",isbn:"978-1-83968-760-0",printIsbn:"978-1-83968-759-4",pdfIsbn:"978-1-83968-761-7",doi:null,price:0,priceEur:0,priceUsd:0,slug:null,numberOfPages:0,isOpenForSubmission:!1,hash:"cc49d6034d85f8f2e2890c6acc3cc629",bookSignature:"Dr. Abhijit Biswas",publishedDate:null,coverURL:"https://cdn.intechopen.com/books/images_new/10285.jpg",keywords:"Mott Insulators, Semi Metals, Polycrystals, Single Crystals, Electronic Properties, Magnetic Properties, PLD, MBE, Topological Insulators, Topological Hall Effect, Devices Applications, Catalysis",numberOfDownloads:null,numberOfWosCitations:0,numberOfCrossrefCitations:null,numberOfDimensionsCitations:null,numberOfTotalCitations:null,isAvailableForWebshopOrdering:!0,dateEndFirstStepPublish:"September 9th 2020",dateEndSecondStepPublish:"October 7th 2020",dateEndThirdStepPublish:"December 6th 2020",dateEndFourthStepPublish:"February 24th 2021",dateEndFifthStepPublish:"April 25th 2021",remainingDaysToSecondStep:"5 months",secondStepPassed:!0,currentStepOfPublishingProcess:5,editedByType:null,kuFlag:!1,biosketch:"A pioneering researcher in the field of tailoring metal oxide crystal surfaces and growth as well as engineering of thin films for various emergent phenomena and energy applications. Dr. Biswas received his Ph.D. from POSTECH, South Korea.",coeditorOneBiosketch:null,coeditorTwoBiosketch:null,coeditorThreeBiosketch:null,coeditorFourBiosketch:null,coeditorFiveBiosketch:null,editors:[{id:"194151",title:"Dr.",name:"Abhijit",middleName:null,surname:"Biswas",slug:"abhijit-biswas",fullName:"Abhijit Biswas",profilePictureURL:"https://mts.intechopen.com/storage/users/194151/images/system/194151.png",biography:"Dr. Abhijit Biswas is a research associate at the Indian Institute of Science Education and Research (IISER) Pune, in India. His research goal is to design and synthesize highest quality epitaxial heterostructures and superlattices, to play with their internal degrees of freedom to exploit the structure–property relationships, in order to find the next-generation multi-functional materials, in view of applications and of fundamental interest. 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Currently, he is also serving as a reviewer of several reputed peer-review journals.\nDr. Biswas received his B.Sc. in Physics from Kalyani University, followed by M.Sc in Physics (specialization in experimental condensed matter physics) from Indian Institute of Technology (IIT), Bombay. His Ph.D., also in experimental condensed matter physics, was awarded by POSTECH, South Korea for his work on the transport phenomena in perovskite oxide thin films. 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1. Introduction
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One of the important biopolymers present in some cereals and fungi is the β-glucan. This polysaccharide plays an important role in the immune system, skin protection, among others. In addition to their cholesterol-lowering and potential cancer-preventing properties, β-glucans may be useful in controlling blood glucose levels. The β-D-glucans from yeast and some plants have been shown to have antitumor and antibacterial activity when injected or ingested by animals in experimentation [1–7].
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Cereal grains, such as barley, oats, and rye, and fungi, such as Aspergillus, Saccharomyces, and mushrooms, contain β-D-glucans [8, 9]. The concentration of β-glucan in oats ranges from 1.9 to 8.0% [10, 11]. In barley grains, these values can reach 3.5–4.8% [12]. These variations are associated with genotype of grain and location and the environmental conditions in which the culture was grown and may result in variation in the quality of β-glucan. This problem is reduced if the source is from microorganisms, which are cultured in defined conditions, and they are not dependent from the location or the environmental conditions.
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2. Chemical structure of β-glucans
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Glucans are glucose polymers, classified according to their interchain linkage as being either α- or β-linked. β-glucans are a heterogeneous group of non-starch polysaccharides, consisting of D-glucose monomers linked by β-glycosidic bonds [13]. The central skeleton of the β-glucans is formed by linear monomers of D-glucose connected at position β-(1-3), with side chains attached to β-(1-6) or β-(1-4)-D-glucopyranosyl unit linkage (Figure 1). In yeast, the skeleton is branching at β-(1-6) and in plants and bacteria at β-(1-4) unit linkage [14–16]. In mushrooms, molecules with binding β-(1-6) and others with connections β-(1-6) and β-(1-4), whether or not linked to protein, were reported [17]. Significant structural differences in β-glucans are characterized by the glycosidic linkage ratios depending on both the source and method of isolation. In the cereal β-glucans, for example, the trisaccharide-to-tetrasaccharide ratios follow the order of wheat (4.2–4.5), barley (2.8–3.3), and oat (2.0–2.4) [18].
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Figure 1.
Polymer of β (1-3)-D-glycopyranosyl units with branching at β (1-6) and β (1-4)-D-glycopyranosyl units.
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3. Biological properties and applications of β-glucans
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In the last decades, the β-glucans have received special attention for its biological activity. Numerous beneficial effects have been attributed to this polymer, in particular due to its immunomodulatory potential. However, beyond the modulatory action of the immune system, several other activities related to β-glucans have been evaluated and proven, as their antitumoral, anti-inflammatory, antimutagenic, and antioxidant action, their hypoglycemic and hypocholesterolemic capacity, and also their protective effect against infections [19]. The β-glucans have a long scientific history, encompassing hundreds of studies. However, this molecule is not properly explored even in therapy, as an additive in food or feed, probably due to its relatively expensive price—about U$ 36/kg (brand Macrogard; Biorigin, Quatá, São Paulo, Brazil). Research involving the biological activity of this polymer originated in the 1940s, with the renowned scientist Pillemer and his colleagues, who obtained a crude-insoluble extract of the cell wall of the Saccharomyces cerevisiae, called zymosan, consisting of proteins, chitin, β-glucan, mannans, and lipids. According to the authors, this extract was able to stimulate the immune response in a non-specific manner [20]. Clinical studies in humans involving the β-glucans began in the 1970s, even before the evidence of their mode of action on the immune system, with reports of curing different types of cancer, including breast cancer, melanoma, and adenosquamous carcinoma of the lung after the application of extracts of β-glucans [21].
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3.1. Immune system and immunomodulatory activity of β-glucans
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The immune system operates seeking to protect the organism from infections that can be caused by various agents, including bacteria, viruses, fungi, and parasites. The cells and molecules of the immune system are highly specialized in the defense against infection. Individuals with a compromised immune defense system due to various factors, such as age, chronic infection, or malnutrition, are subject to several problems, including arthritis, reduced healing capacity, reduced proliferation of bone marrow cells with consequent low defense cell counts, anemia, and increased incidence of all types of microbial infections. Studies also show that one of the main elements of the process of aging is a decrease in the functional effectiveness of the immune system [22]. Among the immunologically competent cells, macrophages play a major role in the initiation and maintenance of immune response both innate and adaptive [15]. In addition to the functions of phagocytosis and the release of lysosomal enzymes, macrophages are also responsible for the release of a number of cytokines and inflammatory mediators can stimulate the immune system in general [22].
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The β-glucan belongs to the class of substances BRMs, or a variety of different substances known as Biological Response Modifiers. being able to trigger a series of events in the immune response [23], increasing the immune defense of the host by activating the functions of cells of the immune system [20]. This polymer is currently considered as one of the most potent stimulators of the immune response, effective both orally or intravenously, completely non-toxic and safe [15]. The response of β-glucan in vertebrates begins with its recognition by receptors present on the cell surface of various immune cells, such as macrophages, neutrophils, dendritic cells, and natural killer cells (NK), and receptors have also been described presently as non-immune cells, endothelial cells, fibroblasts, alveolar epithelial, and Langerhans cells [20]. The various receptors present on the cell membranes of immune cells related to the recognition of β-glucan in vertebrates are dectin-1, complement receptor 3 (CR3), lactosylceramide receptor, Toll-like receptor 2 (TLR-2), and scavenger receptors [24, 25]. The dectin-1 is a type II transmembrane protein with receptor extracellular domain CDR which is responsible for carbohydrate recognition, and a cytoplasmic tail with immunoreceptor ITAM (tyrosine-based activating motif) involved in superoxide production by macrophages in response to the immunosystem defense. The dectin-1 can mediate diverse cellular responses, including phagocytosis and endocytosis. This protein may also induce the production of cytokines and inflammatory chemokines, such as tumor necrosis factor (TNF-α), macrophage inflammatory protein-2 (MIP-2), and interleukin-12 (IL-12) [16]. The receptor CR3 stimulates cytokine secretion by NK cells, especially in the presence of pathogens. This receptor acts as a cell adhesion molecule since it has a binding site for carbohydrates located on the terminal carbon, and thus a receptor for the phagocyte β-glucan [15].
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3.2. Medical application: cancer
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Anticarcinogenic substances are able to reduce, delay, or even prevent the development of malignancies [26]. Different studies have shown anticarcinogenic action of β-glucans and their derivatives [1, 2, 4]. At the end of 1970s, a study on mice with subcutaneous tumor implantation revealed that extracts containing high concentrations of β-glucan significantly reduced growth of mammary carcinomas and melanomas in animals treated and verified an increase in survival of these animals [27]. Kogan et al. [6] observed increased inhibition in the occurrence of lung metastases up to 94% in animals that received oral administration of β-glucan during treatment with cyclophosphamide for Lewis lung carcinoma. Several surveys show the effectiveness of antitumor action of β-glucans in chemotherapy and the improvement in the survival of patients with different types of cancer. A study involving women with malignant breast tumors confirmed the activation and proliferation of monocytes in peripheral blood of patients upon oral administration of β-glucan. According to the researchers, clinical improvement in the survival of patients with no evidence of any recurrent side effects was demonstrated [4]. The effective immune response against tumor cells mediated by β-glucans is based on the activation and expansion of several immune functions, among them the activation of cytotoxic T cells specifically attack cancer cells [28]. The CD4+ T lymphocytes play a role as modulators of immune cells to produce multiple cytokines. The latter are mediators essential for the generation of an effective immune response involving CD8+ T cells, which are necessary for the defense against tumor cells [1]. The effects of β-glucan in lymphocyte activation involving the antitumor immune response have been reported in experimental animal and human models. A study of 30 patients with advanced prostate cancer, who were treated by oral administration of a soluble fraction of β-glucan (carboxymethyl glucan), revealed that after administration there was a significant increase in CD3+, CD4+, and CD8+ in peripheral blood of patients and consequent stimulation of the immune system [2].
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3.3. β-glucans applied in other diseases
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Since β-glucans affect immune function stimulating various immune cell activations, studies were performed to demonstrate the effective application of this immunomodulatory compound in treatment of diseases. Patients with severe periodontitis have failed for the recruitment and activation of macrophages [29]. β-glucans induce macrophage activation and establishment of Th1, and their use may be responsible for the inhibition of tissue destruction in periodontal disease. The use of β-glucan in dental treatment has been systematically evaluated in recent years. Studies with animals showed a significantly reduced periodontal bone loss after oral administration of β-(1-3),(1-6) glucan [30]. Acar et al. [31] investigated the effects of non-surgical periodontal therapy (NPT) with an adjunctive use of systemic β-glucan on clinical, microbiological, and gingival parameters. Their findings showed that β-glucan might increase the concentration of TGF-β1, thereby augmenting periodontal healing potential. Proposals for treating allergic diseases using β-glucans have also been reported. A new therapeutic strategy for allergic diseases using β-glucan was proposed, with beneficial action in restoring the function of type 2 T-helper cells. Through the application of subcutaneous injections in child patients, β-glucan was demonstrated to be able to modulate allergic sensitization in patients, greatly improving their quality of life [32]. Furthermore, the antibacterial, antiviral, and antifungal properties of β-glucan and its derivatives are also reported. Different studies have shown the protective effect of β-glucan to Staphylococcus aureus [33], Pneumocystis carinii, Leishmania donovani, and Influenza virus [22]. The protective effect of β-glucan from S. cerevisiae against DNA damage and cytotoxicity in wild-type (k1) and repair-deficient xrs5 CHO cells were evaluated by Oliveira et al. [34].
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3.4. Food and feed applications of β-glucans
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The search for higher human living standards and greater longevity has generated the need for the development of nutritional alternatives that result in improved general health which means more enjoyment of life, less diseases and less time, and money required for medical needs. In this context, special foods enriched with molecules with health benefits are been developed. Some studies dealing with the enormous benefits of β-glucan as a nutritional supplement [31, 35–37]. Used as adjunctive to the positive effects of antioxidants, lipid balance enhancers, antibiotics, and other therapeutics, the β-glucans are currently considered a true antiaging supplement. These properties are associated with several studies which have shown biological activity of β-glucan, describing its action modulating the immune system and antitumor action [1, 3].
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3.4.1. β-glucan in the human diet
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In recent years, there has been increasing interest in the effect of the use of β-glucan as a dietary supplement. Different studies seek to prove the use of this polysaccharide in the diet has several health benefits. The beneficial effects of consistent intake of β-glucan and its action in reducing cholesterol levels in the blood have been systematically studied. A study of 20 hypercholesterolemic patients, who received daily dietary supplement containing 5.8 g of β-glucan for 4 weeks, reported a 9% decrease in cholesterol level in the intervention group, while there was no difference in the placebo (maltodextrin) group [7]. Nicolosi et al. [38] observed a significant reduction in total and LDL cholesterol in hypercholesterolemic obese patients after 8 weeks of intake of orange juice supplemented with β-glucan. The action of β-glucan on cholesterol reduction can be explained in terms of the reduction in bile reabsorption or the increase in viscosity in the small intestine. However, a more likely explanation relates to the size of the molecule and its subsequent absorption by the intestine. According to Kim et al. [37], molecules of small size, which are consequently less viscous, are less effective in lowering cholesterol. Studies with β-glucan of low molecular size (370,000–1,000,000) reported this polysaccharide ineffective in reducing the cholesterol level [39], whereas Braaten et al. [7] reported a significant reduction in cholesterol levels in the blood of patients who included β-glucan of molecular size above 1.2 million in their diet. β-glucans become a great special food in a diet designed to adjunct in diabetic patients. The action of this polymer in lowering blood glucose level is also reported in the literature. Research has demonstrated the antidiabetic effect of IL-1 cytokine, which increases insulin production, resulting in the lowering of blood glucose levels [40, 41]. Since the β-glucan acts on the activation of macrophages, and these are considered the major source of IL-1 in the human body, this polymer becomes useful in diets designed for diabetic patients. According to Regand et al. [42], the physiological activity of β-glucan in reducing glycemic responses has been mostly attributed to its effect in increasing viscosity in the upper digestive tract. The introduction of β-glucan in the diet may decrease the incidence of colds, respiratory diseases, in addition to alleviating the symptoms caused by these diseases, since this polymer increases the body’s potential to defend against invading pathogens [31]. A study with seventy-five marathon runners showed that daily administration of β-glucan can prevent upper respiratory tract (URTI) symptoms and improve overall health and mood following a competitive marathon [36]. More recently, a study of 162 healthy participants with recurring infections who received a diet supplemented with β-(1-3),(1-6) glucan showed a reduction in the number of symptomatic common cold infections by 25% and the mean symptom score was 15% lower compared to the control group [35].
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3.4.2. β-glucan additives in animal feed
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β-glucan has been prominent among the ingredients used as supplements in animal feed in order to reduce the risk of chronic diseases both in mammals and in fish and birds [43], since they are able to absorb mycotoxins, thus decreasing their toxic effect and mediating their removal from the body [44]. Different food supplements containing β-glucan are available for commercial use for animals. Among them, Bio-Mos® is used in the prevention of infectious diseases of various origins and MTB100® in the elimination of the mycotoxins and inhibition of their toxic effect, both manufactured by Alltech Inc. (Nicholasville, KY). Animals treated with foods supplemented with β-glucan exhibit greater resistance to pathogenic microorganisms, and bacteria or viruses requiring lower dosages of antibiotics or antivirals to deal with infections [5].
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4. Production of purified β-glucan
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4.1. β-glucan extraction and purification by yeast cells
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Many processes and raw materials of obtaining β-glucans have been described, but the challenge is finding the best extraction leading to high purity with the great immunostimulant and antitumor action, periodontal therapy, among others. After the discovery of the benefits of β-glucan for animals and humans, various processes of purification and isolation of this polysaccharide have been developed [44]. The research for new methods of obtaining β-glucan is being conducted prioritizing a non-aggressive extraction, which preserves the most of the original structure of the macromolecule. Currently, β-glucan used as additive in feed is produced by the cultivation of S. cerevisiae or as residue from the fuel ethanol or beer industry. In this respect, just the Brazilian production of sugar cane in the 2012/2013 harvest was 589 million tons of cane and 23.64 billion liters in ethanol was produced [45–47] with expectation of growing. The trading of β-glucan could be increased, since the yeast extraction from the fuel ethanol distilleries up to 5% per day or 7.5 kg powder yeast per m3 ethanol/day would be possible, which could reach at least 177,300 ton of yeast/day, only in the Brazilian fuel ethanol industry.
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4.1.1. Lysis of yeast cell
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The basic process of β-glucan extraction involves the lysis of cells (chemical, biochemical, mechanical, or by autohydrolysis), separation of cell wall (centrifugation or filtration), extraction, and purification (precipitation and centrifugation). The yeast cells are normally processed to produce β-glucan, mannan, and yeast extract. One important aspect of the technology to produce β-glucan and other valuable products from yeasts is the method of cell wall lysis. Yeast autolysis is used in the industrial processes due to the low cost, fractionation efficiency, and quality of products obtained. Firstly, the fresh yeast cells are autolysed, and the cell wall is separated by centrifugation.
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The yeast cell wall has a thickness of 100–200 nm, and the wall is not only for protection and structural function but is also metabolically important [48]. The thickness and structure of the wall could vary depending on several factors like the strain, the industrial process of yeasts, and culture conditions. The concentration of β-glucans also depends on these parameters since the wall is used for the β-glucan extraction. The outer layer of mannoproteins retains the periplasmic proteins conferring resistance to the cells of yeasts and acts as a barrier to external attack of enzymes and some other molecules [49]. The layer of glucan is more internal and linked with chitin in adjacent layers to the plasma membrane and confers rigidity and the cell shape [50].
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Autolysis is an irreversible process caused by intracellular enzymes of yeast under stress conditions, such as temperature, pH, yeast concentrations unsuitable for the survival of the cells. This process is based mainly on heat treatment and causes lysis of the cells from activation of a group of intracellular enzymes that breaks the wall [51]. According to Nagodawithana [51], lysis occurs primarily because of the enzymes β-(1-3) glucanase and protease. Enzymes β-(1-6) glucanases and mannanases participate in solubilizing the matrix of the cell wall, and over forty enzymes have been identified in S. cerevisiae containing a major role in the autolytic process. Probably due to metabolic differences between different strains of S. cerevisiae, several studies disagree on the physicochemical conditions more appropriate for the autolysis of the cells vary from 45 to 55°C in 3–7 days of treatment [52]. The optimization of autolysis of Saccharomyces cerevisiae from a brewery was studied aiming at the maximum ribonucleic acid extraction and yeast extract production [52]. The best conditions for yeast autolysis were 55.2°C, pH = 5.1 and 9.8% NaCl in 24 h of processing. In these conditions, the RNA extraction yield was 89.7%, resulting in 51.3% of dehydrated yeast extract with 57.9% protein, and 48.7% cellular wall with 21.7% protein. The thermal shock at 60°C per 15 min prior to autolysis provided an increase in this yield of 89.7–91.4%. The optimized autolysis including NaCl plasmolysis was efficient, economic, and fast, thus usable for industrial purposes. Currently, yeast residues are exported as yeast flour for feed at low prices by the countries which are producers of fuel ethanol and beer. The improvement of the technology of fractionation and purification in other products like β-glucan, RNA, mannan, mannoprotein, and others is strategic since more valuable products can be produced. This is in accordance with the concept of biorefinery, that is, co-production of biofuels, bioenergy, and marketable chemicals from renewable biomass [53].
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Thereafter, the β-glucan is extracted from autolysed yeast cells by hot alkaline hydrolysis (NaOH) and purified by citric acid precipitation. Another combination of alkali and inorganic acid to extract β-(1-3) glucan was performed by Sandula et al., [54], followed the method described by Machová et al., [55] to obtain water-insoluble β-(1-3) glucan from S. cerevisiae. In this method, 6% NaOH solution at 60°C was also used; however, the extraction was done by 4% phosphoric acid at room temperature [56]. The effects of drying were evaluated in three different processes (lyophilization, spray drying, and solvent precipitation) on the physical properties and immunoregulatory effect of β-glucan of Saccharomyces.
\n
\n
\n
\n
4.2. Chemical modification of β-1,3 glucan
\n
The research of modification of β-1,3 glucan has been performed aiming to improve biological properties. Others steps to obtain modified glucan like methylation, permethylation, carboxymethylation, sulfoethylation, and ultrasonication Depending on the application or use of this molecule. Carboxymethylation of the glucans was made with glucan or chitin–glucan complex suspended in a mixture with 30% NaOH and isopropanol, and stirred at 10°C for 1 h. The degree of substitution of the carboxymethylated glucan was 0.56 or 0.91 for glucan and 0.43 for chitin–glucan complex, depending on the amount of monochloroacetic acid used [57]. The procedure of sulfoethylation of the glucans was performed using sodium β-chloroethylsulfonate in isopropanol solution [58], and permethylation of baker’s yeast glucan was carried out according to Ciucanu & Kerek [59] using powdered NaOH. The immunomodulatory activity was detected in fibrillar (non-soluble) and partially hydrolyzed baker’s yeast glucan as well as its soluble derivatives prepared by carboxymethylation and sulfoethylation. All these glucans showed anti-infective activity against Klebsiella pneumoniae after intravenous or subcutaneous prophylactic application to mice [60].
\n
The evolution of β-(1,3) glucan use in the pharmaceutical and medical areas, as well as food and feed, depends on the development of more economical and efficient methods of extraction, purification, and chemical modification of this interesting molecule. Although their biological properties are amply evidenced, more studies are needed about its application, making this knowledge more available to benefit the health of human and animal.
\n
\n
\n
\n
5. Conclusion
\n
β-(1-3) glucan is a promising healthier food and feed additive whose special properties certified ranging from the activation of the immune system, replacement of antibiotics in animal production, particularly for fish and pork, and various therapies: antitumor, allergic and respiratory diseases, periodontitis and peritonitis. This polymer has also proven to be available as food ingredient for the control of cholesterol and diabetes in special foods. Despite having started their studies for some decades, this molecule remains expensive and not widely available, with the technology dominated by a few producers.
\n
The extraction methods using alkali and acid, with previous pre-treatments, and the step of purification and chemical modification, are needed to obtain β-glucan according to specific biological properties. The solubility, molecular size, level of protein, and degree of methylation are essential parameters to be considered for these properties. This work also highlighted some technological aspects of economic obtaining of β-glucan from yeast.
\n
\n\n',keywords:"β-glucans, chemical properties, extraction, purification, immunostimulating properties",chapterPDFUrl:"https://cdn.intechopen.com/pdfs/50843.pdf",chapterXML:"https://mts.intechopen.com/source/xml/50843.xml",downloadPdfUrl:"/chapter/pdf-download/50843",previewPdfUrl:"/chapter/pdf-preview/50843",totalDownloads:1452,totalViews:655,totalCrossrefCites:1,totalDimensionsCites:2,hasAltmetrics:0,dateSubmitted:"October 16th 2015",dateReviewed:"April 13th 2016",datePrePublished:null,datePublished:"July 13th 2016",dateFinished:null,readingETA:"0",abstract:"Yeasts are a potential source for prebiotic β-glucans. This polysaccharide is characterized by d-glucose monomers linked by β-glycosidic bonds. There are significant structural differences in β-glucans depending on the source and method in which they are obtaining. This polymer is a healthier food and feed additive. Numerous beneficial effects have been attributed to this polymer, in particular immunomodulatory action. Different studies confirm safe use and applicability of β-glucans in medicine for the treatment of diseases (cancer, infections, respiratory diseases) and reduction in glucose and cholesterol levels. Many advances in the processes to obtain β-glucans have been presented, including extraction, purification, and chemical modification, aiming the biological properties and yield. One limitation of their use is the cost, so a strategic discussion of the use of yeast biomass was performed for the production of β-glucans. An extensive and systematic review was undertaken to contribute to the science and technology to obtain β-glucans and their use in different applications.",reviewType:"peer-reviewed",bibtexUrl:"/chapter/bibtex/50843",risUrl:"/chapter/ris/50843",book:{slug:"probiotics-and-prebiotics-in-human-nutrition-and-health"},signatures:"Pedro De Oliva-Neto, Sidmeire Santos Oliveira, Estevão Zilioli and Márcia Zilioli Bellini",authors:[{id:"179544",title:"Dr.",name:"Pedro",middleName:null,surname:"De Oliva-Neto",fullName:"Pedro De Oliva-Neto",slug:"pedro-de-oliva-neto",email:"pedroolivaneto@gmail.com",position:null,institution:{name:"Sao Paulo State University",institutionURL:null,country:{name:"Brazil"}}},{id:"181094",title:"Dr.",name:"Márcia",middleName:null,surname:"Zilioli-Bellini",fullName:"Márcia Zilioli-Bellini",slug:"marcia-zilioli-bellini",email:"mzbellini@gmail.com",position:null,institution:null},{id:"181096",title:"Dr.",name:"Estevão",middleName:null,surname:"Zilioli",fullName:"Estevão Zilioli",slug:"estevao-zilioli",email:"estevaoz@gmail.com",position:null,institution:null},{id:"181097",title:"MSc.",name:"Sidmeire",middleName:null,surname:"Santos-Oliveira",fullName:"Sidmeire Santos-Oliveira",slug:"sidmeire-santos-oliveira",email:"meiri_soliveira@hotmail.com",position:null,institution:null}],sections:[{id:"sec_1",title:"1. Introduction",level:"1"},{id:"sec_2",title:"2. Chemical structure of β-glucans",level:"1"},{id:"sec_3",title:"3. Biological properties and applications of β-glucans",level:"1"},{id:"sec_3_2",title:"3.1. Immune system and immunomodulatory activity of β-glucans",level:"2"},{id:"sec_4_2",title:"3.2. Medical application: cancer",level:"2"},{id:"sec_5_2",title:"3.3. β-glucans applied in other diseases",level:"2"},{id:"sec_6_2",title:"3.4. Food and feed applications of β-glucans",level:"2"},{id:"sec_6_3",title:"3.4.1. β-glucan in the human diet",level:"3"},{id:"sec_7_3",title:"3.4.2. β-glucan additives in animal feed",level:"3"},{id:"sec_10",title:"4. Production of purified β-glucan",level:"1"},{id:"sec_10_2",title:"4.1. β-glucan extraction and purification by yeast cells",level:"2"},{id:"sec_10_3",title:"4.1.1. Lysis of yeast cell",level:"3"},{id:"sec_12_2",title:"4.2. Chemical modification of β-1,3 glucan",level:"2"},{id:"sec_14",title:"5. Conclusion",level:"1"}],chapterReferences:[{id:"B1",body:'\nMagnani, M., Castro-Gómez, R.J.H., Mori, M.P., Kuasne, H., Gregório, E.P., Libos Jr., F. & Cólus, I.M.S. (2011a). Protective effect of carboxymethyl-glucan (CM-G) against DNA damage in patients with advanced prostate cancer. Genetics and Molecular Biology, 34(1), 131–135.'},{id:"B2",body:'\nMagnani, M., Castro-Gómez, R.J.H., Aoki, M.N., Gregório, E.P. & Libos Jr, F. Morimoto, H.K., Reiche, E.M.V. & Watanabe, M.A.E. (2011b). Analysis of peripheral T cells and the CC chemokine receptor (CCR5) delta32 polymorphism in prostate cancer patients treated with carboxymethyl-glucan (CM-G). Natural Product Research: Formerly Natural Product Letters, 26(10), 945–951.'},{id:"B3",body:'\nMurakawa, K., Fukunaga, K., Tanouch, M., Hosokawa, M., Hossan, Z. & Takahashi, K. (2007). Therapy of myeloma in vivo using marine phospholipid in combination with Agaricus blazei Murill as an immune respond activator. Journal of Oleo Science, 56(4), 179–188.'},{id:"B4",body:'\nDemir, G., Klein, H.O., Mandel-Molinas, N. & Tuzuner, N. (2007). β-glucan induces proliferation and activation of monocytes in peripheral blood of patients with advanced breast cancer. International Immunopharm, 7, 113–116.'},{id:"B5",body:'\nXiao, Z., Trincado, C.A. & Murtaugh, M.P. (2004). β-Glucan enhancement of T cell IFN-gamma response in swine. Veterinary Immunology and Immunopathology, 102(3), 315–320.'},{id:"B6",body:'\nKogan, G., Šandula, J., Korolenko, T.A., Falameeva, O.V., Poteryaeva, O.N., Zhanaeva, S.Ya., Levina, O.A., Filatova, T.G. & Kaledin, V.I. (2002). Increased efficiency of Lewis lung carcinoma chemotherapy with a macrophage stimulator—yeast carboxymethyl glucan. International Immunopharmacol, 2, 775–781.'},{id:"B7",body:'\nBraaten, J.T., Wood, P.J., Scott, F.W., Wolynetz, M.S., Lowe, M.K., Bradley-White, P. & Collins, M.W. (1994). 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(1992). Effect of β-glucan, starch, and fibre content and steam vs. dry rolling of barley grain on its degradability and utilization by steers. Animal Feed Science and Technology, 37(2), 33–46.'},{id:"B13",body:'\nEl Khoury, D., Cuda, C., Luhovyy, B.L. & Anderson, G.H. (2012). Beta glucan: health benefits in obesity and metabolic syndrome. Journal of Nutrition and Metabolism, 2012: 28. doi:10.1155/2012/851362.'},{id:"B14",body:'\nMagnani, M. & Castro-Gómez, R.J.H. (2008). β-glucan from Saccharomyces cerevisiae: constitution, bioactivity and obtaining. Semina: Ciencias Agrarias, 29(3), 631–650.'},{id:"B15",body:'\nChan, G.C., Chan, W.K. Sze, D.M. (2009). The effects of β-glucan on human immune and cancer cells. Journal of Hematology & Oncology, 2, 25–36.'},{id:"B16",body:'\nStone, B.A. & Clarke, A.E. (1992). Chemistry and biology of (1,3)-D-glucans. La Trobe University, Victoria, Australia Press.'},{id:"B17",body:'\nCamelini, C.M., Mendonça, M., Dias, P.F. & Maraschin, M. (2005). β-glucans from mushrooms. Biotecnologia Ciencia e Desenvolvimento, 35, 36–47.'},{id:"B18",body:'\nLi, W., Cui, S.W. & Kakuda, Y. (2005). Extraction, fractionation, structural and physical characterization of wheat β-D-glucans. Carbohydrate Polymers, 63, 408–416.'},{id:"B19",body:'\nJantova, S., Bakos, D., Birosova, L. & Matejov, P. (2015). Biological properties of a novel coladerm-beta glucan membrane. In vitro assessment using human fibroblasts. Biomed Papers of Medical Faculty of the University Palacky Olomouc, Czech Repub, 159(1):67–76. doi: 10.5507/bp.2012.115.'},{id:"B20",body:'\nBrown, G.D. & Gordon, S. (2003). Fungal β-glucans and mammalian immunity. Immunity, 19(3), 311–315.'},{id:"B21",body:'\nMansell, P.W.A., Ichinose, I.I., Reed, R.J., Krements, E.T., McNamee, R.B. & Di Luzio, N.R. (1975). Macrophage-mediated destruction of human malignant cells in vive. Journal of the National Cancer Institute, 54, 571–580.'},{id:"B22",body:'\nAkramienė, D., Kondrotas, A., Didžiapetrienė, J. & Kėvelaitis, E. (2007). Effects of β-glucans on the immune system. Medicina (Kaunas), 43(8), 597–606.'},{id:"B23",body:'\nBohn, J.A. & BeMiller, J.M. (1995). (1-3)-β-D-glucans as biological response modifiers: a review of structure-functional activity relationships. Carbohydrate Polymers, 28 (1), 3–14.'},{id:"B24",body:'\nKwiatkowski, S., Kwiatkowski, S.E. Yeast (Saccharomyces cerevisiae) Glucan Polysaccharides—Occurrence, Separation and Application in Food, Feed and Health Industries. (2012). In: D.N. Karunaratne (Ed.), The Complex World of Polysaccharides, (47–70), In Tech, Rijeka, Croatia. http://dx.doi.org/10.5772/48100.'},{id:"B25",body:'\nBattle, J., Ha, T., Li, C., Della Beffa, V., Rice, P., Kalbfleisch, J., Browder, W. & Williams, D. (1998). Ligand binding to the (1-3)-β-D-glucan receptor stimulates NFkB activation, but not apoptosis in U937 cells. Biochemical and Biophysical Research Communications, 249(2), 499–504.'},{id:"B26",body:'\nKuroda, Y. & Hara, Y. (1999). Antimutagenic and anticarcinogenic activity of tea polyphenols. Mutation Research, 436(1), 69–97.'},{id:"B27",body:'\nDi Luzio, N.R. (1983). Immunopharmacology of glucan: a broad spectrum enhancer of host defense mechanisms. Trends in Pharmacological Sciences, 4, 344–347.'},{id:"B28",body:'\nManners, D.J., Mason, A.J. & Patterson, J.C. (1973). The structure of a 1,3 β-glucan from yeast cell walls. Biochemistry Journal, 135, 19–30.'},{id:"B29",body:'\nChaple, C.C., Srivastrava, M. & Hunter, N. (1998). Failure of macrophage activation in destructive periodontal disease. The Journal of Pathology, 186, 281–286.'},{id:"B30",body:'\nHartland, R.P., Vermeulen, C.A., Sietsma, J.H., Wessels, J.G.H. & Klis, F.M. (1994). The linkage of (1-3)-β-glucan to chitin during cell wall assembly in Saccharomyces cerevisiae. Yeast (Chichester, England), 10(12), 1591–1599.'},{id:"B31",body:'\nAcar, N.N., Noyan, U., Kuru, L., Kadir, T. & Kuru, B. (2012). Adjunctive Systemic Use of Beta-Glucan in the Nonsurgical Treatment of Chronic Periodontitis. In N. Budeneli (Ed.), Pathogenesis and Treatment of Periodontitis, (pp. 167–182). Shanghai: In Tech China.'},{id:"B32",body:'\nSarinho, E., Medeiros, D., Schor, D., Silva, A.R., Sales, V., Motta, M.E., Costa, A., Azoubel, A. & Rizzo, J.A. (2009). Production of interleukin-10 in asthmatic children after beta-1-3-glucan. Allergol Immunopathol, 37, 188–192.'},{id:"B33",body:'\nDi Luzio, N.R. & Williams, D.L. (1978). Protective effect of glucan against systemic Staphylococcus aureus septicemia in normal and leukemic mice. Infection and Immunity, 20, 804–810.'},{id:"B34",body:'\nOliveira, R.J., Matuo, R., da Silva, A.F., Matiazi, H.J., Mantovani, M.S. & Ribeiro, L.R. (2007). Protective effect of β-glucan extracted from Saccharomyces cerevisiae against DNA damage and cytotoxicity in wild-type (k1) and repair-deficient xrs5 CHO cells. Toxicology In Vitro: An International Journal Published in Association with BIBRA, 21, 41–52.'},{id:"B35",body:'\nAuinger, A., Riede, L., Bothe, G., Busch, R. & Gruenwald, J. (2013). Yeast (1,3)-(1,6)-beta-glucan helps to maintain the body’s defense against pathogens: a double-blind, randomized, placebo controlled, multicentric study in healthy subjects. European Journal of Nutrition, 52(8), 1913–1918.'},{id:"B36",body:'\nTalbott, S. & Talbott, J. (2009). Effect of Beta 1,3/1,6 Glucan on upper respiratory tract infection symptoms and mood state in marathon athletes. Journal of Sports Science and Medicine, 8, 509–515.'},{id:"B37",body:'\nKim, S.Y., Song, H.J., Lee, Y.Y., Cho, K. & Roh, Y.K. (2006). Biomedical Issues of Dietary fiber –Glucan. Journal of Korean Medical Science, 21, 781–789.'},{id:"B38",body:'\nNicolosi, R., Bell, S.J., Bistrian, B.R., Greenberg, I., Forse, R.A. & Blackburn, G.L. (1999). Plasma lipid changes after supplementation with β-glucan fiber from yeast. American Journal of Clinical Nutrition, 70(2), 208–212.'},{id:"B39",body:'\nBeer, M.U., Arrigoni, E. & Amado, R. (1995). Effects of oat gum on blood cholesterol levels in healthy young men. European Journal of Clinical Nutrition, 49, 517–22.'},{id:"B40",body:'\nLang, C.H. & Dobrescu, C. (1989). Interleukin-l induced increases in glucose utilization are insulin mediated. Life Sciences 45(22), 27–34.'},{id:"B41",body:'\nRobertsen, B., Engstad, R.E. & Jorgensen, J.B. (1994). Beta-glucans as Immunostimulants in fish. Modulators of Fish Immune Responses, 1, Fair Haven, NJ, USA.'},{id:"B42",body:'\nRegand, A., Tosh, S.M., Wolever, T.M.S. & Wood, P.J. (2009). Physicochemical properties of β-glucan in differently processed oat foods influence glycemic response. Journal of Agricultural and Food Chemistry, 57, 8831–8838.'},{id:"B43",body:'\nKogan, G. & Kocher, A. (2007). Role of yeast cell wall polysaccharides in pig nutrition and health protection. Livestock Science, 109, 161–165.'},{id:"B44",body:'\nLi, J., Li, D.F., Xing, J.J., Cheng, Z.B. & Lai, C.H. (2006). Effects of β-glucan extracted from Saccharomyces cerevisiae on growth performance, and immunological and somatotropic responses of pigs challenged with Escherichia coli lipopolysaccharide. Journal of Animal Science, 84, 2374–2381.'},{id:"B45",body:'\nMAPA—Brazilian Department of Agriculture, Livestock and Supply (2013). http://www.agricultura.gov.br/vegetal/safras-estoques. Access in the site: April 23, 2014.'},{id:"B46",body:'\nCONAB Brazilian National Company of Supply. (2013). Site: http://www.conab.gov.br/OlalaCMS/uploads/arquivos/13_04_09_10_30_34_boletim_cana_portugues_abril_2013_4o_lev.pdf. Access in the site: Access in: April, 2014.'},{id:"B47",body:'\nAguiar, C. (2011). STAB congress of sugar and ethanol. Management practices and Sustainability. Access site: http://www.stab.org.br/12sba/5.CLEBERAGUIAR.SAOMANOEL.26.10.11hrs.pdf'},{id:"B48",body:'\nDzienzak, J.D. (1987). Yeast and Yeast derivatives applications. Food Technology, 41(2), 122–125.'},{id:"B49",body:'\nKopecká, M., Phaff, H.J. & Fleet, G.H. (1974). Demonstration of a fibrillar component in the cell wall of the yeast Saccharomyces cerevisiae and its chemical nature. The Journal of Cell Biology, 62(1), 66–76.'},{id:"B50",body:'\nKapteyn, J.C., Ram, A.F., Gross, E.M., Kollar, R., Montijn, R.C., Van Den Ende, H., Llobel, A.A., Cabib, E. & Klis, F.M. (1997). Altered extent of cross-linking of β 1,6-glucosylated mannoproteins to chitin in Saccharomyces cerevisiae mutants with reduced cell wall β 1,3 glucan content. Journal of Bacteriology, 179(20), 6279–6284.'},{id:"B51",body:'\nNagodawithana, T. (1992). Yeast-derived flavors and flavor enhancers and their probable mode of action. Food Technology, 46, 138–144.'},{id:"B52",body:'\nOliveira, A.M. & Oliva-Neto, P. (2011). Improvement in RNA extraction from S. cerevisie by optimization in the autolysis and NH3 hydrolysis. Brazilian Archives of Biology and Technology, 54, 1007–1018.'},{id:"B53",body:'\nCherubini, F. & Ulgiati, S. (2010), Crop residues as raw materials for biorefinery systems—A LCA case study. Applied Energy, 87, 47–57.'},{id:"B54",body:'\nSandula, J., Kogan, G., Kacuráková, M. & Machová, E. (1999). Microbial (1-3)-β-D-glucan their preparation, physico-chemical characterization and immunomodulatory activity. Carbohydrate Polymer, 38, 247–253.'},{id:"B55",body:'\nMachová, E., Kogan, G. Alfóldi, J., Soltes, L. & Sandula, J.(1995). Enzymatic and ultrasonic depolymerization of carboxymethylated β(1-3)-D-glucans derived from S. cerevisiae. Journal of Applied Polymer Science, 55, 699–704.'},{id:"B56",body:'\nTorronen, R., Kansanen, L., Uusitupa, M., Hanninen, O., Myllymaki, O., Harkonen, H. & Malkki, Y. (1992). Effects of an oat bran concentrate on serum lipids in free-living men with mild to moderate hypercholesterolaemia. European Journal of Clinical Nutrition, 46, 621–627.'},{id:"B57",body:'\nJamas, S., Easson, D.D. & Ostroff, G.R. (1997). Glucan preparation. US Patent 5622939.'},{id:"B58",body:'\nPastýr, J., Sandula, J., Master, L., Trnovec, T. & Benes, G. (1997). Preparation of water-soluble sulfoderivatives of microbial β(1-3)-D-glucans. Slovak Patent no. 278783.'},{id:"B59",body:'\nCiucanu, I. & Kerek, F. (1984). A simple and rapid method for the permethylation of carbohydrates. Carbohydr Res., 131, 209–217.'},{id:"B60",body:'\nKogan, G., Master, C., Sandula, J., Navarová, J. & Trnovec, T. (1989). Recent results on the structure and immunomodulating activities of yeast glucan. In V. Crescenzi, I.C.M. Dea, S. Pruletti, S.S. Stivala, I.W. Sutherland (Eds). Biochemical and Biotechnological Advances in Industrial Polysaccharides. Elsevier. New York.'}],footnotes:[],contributors:[{corresp:"yes",contributorFullName:"Pedro De Oliva-Neto",address:"pedroolivaneto@gmail.com",affiliation:'
São Paulo State University (UNESP)—School of Sciences and Languages of Assis, Brazil
Integrated Adamantinenses Colleges (FAI), Adamantina, Brazil
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Cutler",authors:[{id:"76407",title:"Dr.",name:"Stephen",middleName:null,surname:"Cutler",fullName:"Stephen Cutler",slug:"stephen-cutler"},{id:"76409",title:"Dr.",name:"Afeef",middleName:null,surname:"Husni",fullName:"Afeef Husni",slug:"afeef-husni"}]},{id:"32949",title:"Alkaloids and Anthraquinones from Malaysian Flora",slug:"alkaloids-and-anthraquinones-from-malaysian-flora",signatures:"Nor Hadiani Ismail, Asmah Alias and Che Puteh Osman",authors:[{id:"67720",title:"Prof.",name:"Nor Hadiani",middleName:null,surname:"Ismail",fullName:"Nor Hadiani Ismail",slug:"nor-hadiani-ismail"},{id:"73827",title:"Ms.",name:"Asmah",middleName:null,surname:"Alias",fullName:"Asmah Alias",slug:"asmah-alias"},{id:"73828",title:"Ms.",name:"Che Puteh",middleName:null,surname:"Osman",fullName:"Che Puteh Osman",slug:"che-puteh-osman"}]},{id:"32950",title:"Phytochemistry of some Brazilian Plants with Aphrodisiac Activity",slug:"phytochemistry-of-some-brazilian-plants-with-aphrodisiac-activity",signatures:"Cinara V. da Silva, Fernanda M. Borges and Eudes S. Velozo",authors:[{id:"68493",title:"MSc.",name:"Cinara",middleName:"Vasconcelos",surname:"Da Silva",fullName:"Cinara Da Silva",slug:"cinara-da-silva"},{id:"75727",title:"Prof.",name:"Eudes",middleName:null,surname:"Velozo",fullName:"Eudes Velozo",slug:"eudes-velozo"},{id:"76095",title:"BSc.",name:"Fernanda",middleName:null,surname:"Borges",fullName:"Fernanda Borges",slug:"fernanda-borges"}]},{id:"32951",title:"A Phytochemical and Ethnopharmacological Review of the Genus Erythrina",slug:"a-phytochemical-and-ethnopharmacological-review-of-the-genus-erythrina",signatures:"João X. de Araújo-Júnior, Mariana S.G. de Oliveira, Pedro G.V. Aquino, Magna S. Alexandre-Moreira and Antônio E.G. Sant'Ana",authors:[{id:"68518",title:"Dr.",name:"João Xavier",middleName:null,surname:"de Araújo-Júnior",fullName:"João Xavier de Araújo-Júnior",slug:"joao-xavier-de-araujo-junior"},{id:"79530",title:"MSc.",name:"Mariana Santos Gomes",middleName:null,surname:"De Oliveira",fullName:"Mariana Santos Gomes De Oliveira",slug:"mariana-santos-gomes-de-oliveira"},{id:"79532",title:"Dr.",name:"Pedro",middleName:"Gregorio Vieira",surname:"Aquino",fullName:"Pedro Aquino",slug:"pedro-aquino"},{id:"79533",title:"Dr.",name:"Magna Suzana",middleName:null,surname:"Alexandre-Moreira",fullName:"Magna Suzana Alexandre-Moreira",slug:"magna-suzana-alexandre-moreira"},{id:"79536",title:"Dr.",name:"Antônio Euzébio Goulart",middleName:null,surname:"Sant'Ana",fullName:"Antônio Euzébio Goulart Sant'Ana",slug:"antonio-euzebio-goulart-sant'ana"}]},{id:"32952",title:"Phytochemistry, Pharmacology and Agronomy of Medicinal Plants: Amburana cearensis, an Interdisciplinary Study",slug:"phytochemistry-pharmacology-and-agronomy-of-medicinal-plants-amburana-cearensis-an-interdisciplinary",signatures:"Kirley M. Canuto, Edilberto R. Silveira, Antonio Marcos E. Bezerra, Luzia Kalyne A. M. Leal and Glauce Socorro B. Viana",authors:[{id:"71155",title:"Dr.",name:"Kirley",middleName:"Marques",surname:"Canuto",fullName:"Kirley Canuto",slug:"kirley-canuto"},{id:"76136",title:"Prof.",name:"Edilberto R.",middleName:null,surname:"Silveira",fullName:"Edilberto R. Silveira",slug:"edilberto-r.-silveira"},{id:"76139",title:"Prof.",name:"Antonio Marcos E.",middleName:null,surname:"Bezerra",fullName:"Antonio Marcos E. Bezerra",slug:"antonio-marcos-e.-bezerra"},{id:"76234",title:"Prof.",name:"Luzia Kalyne A. M.",middleName:null,surname:"Leal",fullName:"Luzia Kalyne A. M. Leal",slug:"luzia-kalyne-a.-m.-leal"},{id:"76238",title:"Prof.",name:"Glauce Socorro B.",middleName:null,surname:"Viana",fullName:"Glauce Socorro B. Viana",slug:"glauce-socorro-b.-viana"}]},{id:"32953",title:"General Introduction on Family Asteracea",slug:"genus-matricaria-chemistry-and-pharmacology",signatures:"Maha Aboul Ela, Abdalla El-Lakany and Mohamad Ali Hijazi",authors:[{id:"75980",title:"Prof.",name:"Maha",middleName:null,surname:"Aboul Ela",fullName:"Maha Aboul Ela",slug:"maha-aboul-ela"},{id:"75990",title:"Prof.",name:"Abdalla",middleName:"Mohamad",surname:"El-Lakany",fullName:"Abdalla El-Lakany",slug:"abdalla-el-lakany"},{id:"75992",title:"MSc.",name:"Mohamad Ali",middleName:null,surname:"Hijazi",fullName:"Mohamad Ali Hijazi",slug:"mohamad-ali-hijazi"}]},{id:"32954",title:"Bioavailability of Phytochemicals",slug:"bioavailability-of-phytochemicals",signatures:"Indah Epriliati and Irine R. Ginjom",authors:[{id:"67608",title:"Dr.",name:"Indah",middleName:null,surname:"Epriliati",fullName:"Indah Epriliati",slug:"indah-epriliati"}]},{id:"32955",title:"Ximenia americana: Chemistry, Pharmacology and Biological Properties, a Review",slug:"ximenia-americana-chemistry-pharmacology-and-biological-properties-a-review",signatures:"Francisco José Queiroz Monte, Telma Leda Gomes de Lemos, Mônica Regina Silva de Araújo and Edilane de Sousa Gomes",authors:[{id:"56270",title:"Dr.",name:"Francisco José",middleName:null,surname:"Queiroz Monte",fullName:"Francisco José Queiroz Monte",slug:"francisco-jose-queiroz-monte"},{id:"57275",title:"Dr.",name:"Telma Leda",middleName:null,surname:"Gomes De Lemos",fullName:"Telma Leda Gomes De Lemos",slug:"telma-leda-gomes-de-lemos"},{id:"57276",title:"Dr.",name:"Monica Regina",middleName:null,surname:"Silva De Araujo",fullName:"Monica Regina Silva De Araujo",slug:"monica-regina-silva-de-araujo"},{id:"119872",title:"Ms.",name:"Edilane",middleName:null,surname:"Gomes",fullName:"Edilane Gomes",slug:"edilane-gomes"}]},{id:"32956",title:"Phytochemicals and Their Pharmacological Aspects of Acanthopanax koreanum",slug:"phytochemicals-and-their-pharmacological-aspects-of-acanthopanax-koreanum",signatures:"Young Ho Kim, Jeong Ah Kim and Nguyen Xuan Nhiem",authors:[{id:"66128",title:"Prof.",name:"Young Ho",middleName:null,surname:"Kim",fullName:"Young Ho Kim",slug:"young-ho-kim"},{id:"66830",title:"Dr.",name:"Jeong Ah",middleName:null,surname:"Kim",fullName:"Jeong Ah Kim",slug:"jeong-ah-kim"},{id:"66831",title:"Associate Prof.",name:"Nguyen Xuan",middleName:null,surname:"Nhiem",fullName:"Nguyen Xuan Nhiem",slug:"nguyen-xuan-nhiem"}]},{id:"32957",title:"Polyphenol Antioxidants and Bone Health: A Review",slug:"phytochemical-antioxidants-and-bone-health-a-review",signatures:"L.G. Rao, N. Kang and A.V. Rao",authors:[{id:"82663",title:"Dr.",name:"Venketeshwer",middleName:null,surname:"Rao",fullName:"Venketeshwer Rao",slug:"venketeshwer-rao"}]},{id:"32958",title:"The Pentacyclic Triterpenes , -amyrins: A Review of Sources and Biological Activities",slug:"the-pentacyclic-triterpenes-amyrins-a-review-of-sources-and-biological-activities",signatures:"Liliana Hernández Vázquez, Javier Palazon and Arturo Navarro-Ocaña",authors:[{id:"69449",title:"Dr.",name:"Arturo",middleName:null,surname:"Navarro-Ocaña",fullName:"Arturo Navarro-Ocaña",slug:"arturo-navarro-ocana"}]},{id:"32959",title:"Phytochemical Studies of Fractions and Compounds Present in Vernonanthura Patens with Antifungal Bioactivity and Potential as Antineoplastic",slug:"phytochemical-studies-of-fractions-and-compounds-present-in-vernonanthura-patens-with-antifungal-bio",signatures:"Patricia Isabel Manzano Santana, Mario Silva Osorio, Olov Sterner and Esther Lilia Peralta Garcìa",authors:[{id:"75995",title:"Dr.",name:"Patricia Isabel",middleName:null,surname:"Manzano Santana",fullName:"Patricia Isabel Manzano Santana",slug:"patricia-isabel-manzano-santana"},{id:"120150",title:"Dr.",name:"Esther Lilia",middleName:null,surname:"Peralta Garcìa",fullName:"Esther Lilia Peralta Garcìa",slug:"esther-lilia-peralta-garcia"},{id:"120151",title:"Dr.",name:"Mario",middleName:null,surname:"Silva Osorio",fullName:"Mario Silva Osorio",slug:"mario-silva-osorio"},{id:"149222",title:"Dr.",name:"Olov",middleName:null,surname:"Sterner",fullName:"Olov Sterner",slug:"olov-sterner"}]},{id:"32960",title:"The Inhibitory Effect of Natural Stilbenes and Their Analogues on Catalytic Activity of Cytochromes P450 Family 1 in Comparison with Other Phenols - Structure and Activity Relationship",slug:"the-inhibitory-effect-of-natural-stilbenes-and-their-analogs-on-catalytic-activity-of-cytochromes-p4",signatures:"Renata Mikstacka, Zbigniew Dutkiewicz, Stanisław Sobiak and Wanda Baer-Dubowska",authors:[{id:"71011",title:"Dr.",name:"Renata",middleName:null,surname:"Mikstacka",fullName:"Renata Mikstacka",slug:"renata-mikstacka"},{id:"119842",title:"Dr.",name:"Zbigniew",middleName:null,surname:"Dutkiewicz",fullName:"Zbigniew Dutkiewicz",slug:"zbigniew-dutkiewicz"},{id:"119844",title:"Prof.",name:"Stanisław",middleName:null,surname:"Sobiak",fullName:"Stanisław Sobiak",slug:"stanislaw-sobiak"},{id:"119845",title:"Prof.",name:"Wanda",middleName:null,surname:"Baer-Dubowska",fullName:"Wanda Baer-Dubowska",slug:"wanda-baer-dubowska"}]}]}]},onlineFirst:{chapter:{type:"chapter",id:"72259",title:"Cell Cycle and Factors Involved in Inhibition or Progression of Breast Cancer",doi:"10.5772/intechopen.92576",slug:"cell-cycle-and-factors-involved-in-inhibition-or-progression-of-breast-cancer",body:'
1. Introduction
Deregulation in cell cycle is a remarkable feature of tumor cells [1, 2]. Cell cycle helps to maintain homeostasis of normal cell growth and viability in a compact process. Cell cycle occurs in four phases as follows:
preparation for cell division in G1 phase;
process of DNA synthesis in S phase;
G2 phase for cell growth and enzyme production; and
mitosis: M phase, which is regulated by several controlled events, directs the replication of DNA and cell division [3].
The transitions between G1 to S and G2 to M phase are governed by changes in the kinase activity of CDKs [4]: Cdk1, Cdk2, Cdk4, Cdk6, and cyclins. Cyclins are the regulatory units, and CDKs contain the catalytic subunit of an activated heterodimer. The cyclin binds to CDKs and gets activated by forming CDK/cyclin complex by phosphorylation leading the dividing cell into next phase of cell cycle. During G1 phase, the predominant cyclin-CDK complexes are cyclin D-Cdk4, 6, cyclin E-Cdk2, cyclin A-Cdk2 during S phase, cyclin A-Cdk1, and cyclin B-Cdk1 during G2/mitotic phases. The control of the G2/M transition is important in all cancers resulting in chromosomal aberrations, but the G1/S transition involves many of the important cell-cycle events that may be altered in breast cancer. G1/S transition involves functions of the oncogenes/tumor suppressors cyclin E, cyclin D1, and p27 [5]. The oncogenic processes do occur by targeting the regulators of G1 phase progression [6]. During the G phase, cells respond to extracellular signals by either going into next division or withdraw from the cycle and thus are arrested in a state (Go). G1 progression is dependent on stimulation by mitogens or growth factors and can be blocked by anti-proliferative cytokines, but cancer cells do not obey these controls. Cancer cells remain in a continuous cycle of cell division by halting maturation and terminal differentiation. Once the cells pass a restriction point late in G1, they do not respond to extracellular growth regulatory signals and commit themselves to the independent program that causes cell division. The cells, which pass through the restriction point G1 and enter into S phase, which is controlled by cyclin-dependent protein kinases (CDKs) that are regulated by cyclins D, E, and A, are committed to divide.
Cyclin D acts as growth factor regulator in response to extracellular signals in the cell cycle. The activity of Cyclin D depends on mitogenic stimulation upon binding with CDK4 and CDK6. Once bound, the catalytic activity of this complex is maximum in G1-S phase transition, but withdrawal of mitogen causes stoppage of cyclin D synthesis, and thus, the D cyclins holoenzyme activities decay rapidly, and the cells exit the cycle [7]. So, if cyclin DI-dependent kinase activity is lost before the restriction point, it prevents cells from entering S phase [8]. To pass through first check point – G1 phase that occurs in normal cell cycle, cyclin D-dependent kinases should phosphorylate protein retinoblastoma tumor suppressor protein (RB) [9]. As the hyper-phosphorylated RB gets dissociated from E2f, DP1, RB complex will result in the activation of E2F genes and leads to transcription of several genes such as cyclin E, cyclin A, and DNA polymerase. RB and other RB-like proteins (pI30, P107), which regulate gene expression which in turn are regulated by a family of heterodimeric transcriptional regulator E2Fs [10], which can transactivate genes and are required for S phase entry [11]. INK4 proteins inhibit (inhibitors of CDK4 and CDK6 INK4 proteins can directly block cyclin D-dependent kinase activity and cause G1 phase arrest) cyclin D-dependent kinases that phosphorylate RB. RB pathway does not functioning normal, which is feature of cancer cells [12]. The RB is inactivated by phosphorylation or by DNA damage; RB gene causes shrinking of G1 phase, and cell size is decreased. The mitogens and other signals required for cell are still present [13]. As the RB negative cells have few requirements for growth factors, these factors in addition to RB phosphorylation work for restriction point control [14]. As the cell cycle proceeds, the cyclin A- and cyclin B-dependent kinases keep RB in its hyper-phosphorylated state. RB is not dephosphorylated until mitosis is completed and again renters the GI phase or Go. The activity of cyclin A synthesis occurs later in GI and is important for the G1-S transition, as blockage of cyclin A function in cells can also block S phase entry. For cell cycle progression, the inactivation of cyclin E and E2F is important when the cell enters S phase [15]. Cyclin B, B-cdc2 complex leads to stimulation of nuclear envelope and initiation of prophase, but its deactivation leads the cell to exit mitosis [16].
2. Drug resistance
Hindrance in treating cancer patient mainly occurs by drug resistance [17]. Targeted therapies on breast cancer depend on the type of receptor being implicated by the expression of estrogen receptor (ER), progesterone receptor (PR), and overexpression of Her2/neu [17]. The therapeutic agents given in such cases, which eventually develop resistance as an acquired drug resistance, are clinically bigger challenge to treat. Thus, patient’s resistant to chemotherapy has poor prognosis and overall poor survival [18].
2.1 Cell cycle regulation in tamoxifen-resistant breast cancers
The main drug given to patients expressing estrogen receptor is tamoxifen, which is the first therapeutic agent for the estrogen or progesterone receptor expressing breast cancers, mostly in premenopausal women with or without conventional chemotherapeutic agents [19]. The estrogen receptor (ER) induction occurs during G0/G1 phase in MCF-7 cells and breast cancer cells [19]. In the late S-phase, a rapid increase in ER has been reported [19]. A tamoxifen-resistant phenotype was developed by long-term exposure of MCF-7 xenografts to tamoxifen resulted in an altered expression of ER during the G0/G1 phase [19]. It has been shown that tamoxifen-resistant MCF-7 cells express higher levels of cell cycle regulators cyclin E1 and CDK2 than parental cells [20]. It has been shown that cyclins E1 and E2 were overexpressed in the tamoxifen-resistant cells when compared with parental MCF-7 cells [20]. TAMR cells may be dependent on cyclin E more than MCF-7C, which indicates that CDK2 is inhibited and is a potential therapeutic marker in endocrine-resistant breast cancer [20]. Cyclin E2 downregulation is required for anti-estrogen inhibition of cell proliferation; cyclin E2 overexpression is associated with endocrine resistance in breast cancer providing reason for deregulation of the cell cycle in endocrine resistance [21, 22, 23, 24].
3. Genes associated with breast cancer development and its progression
There are various genes associated with breast cancer, and how these respond to different treatments are mentioned as follows:
3.1 EGFR
Epidermal growth factor receptor EGFR (ERBB1 or HER1) is from ERBB family of cell-surface receptor tyrosine kinases including HER2, also known as NEU or ERBB2 [25, 26]. The epidermal growth factor receptor family consists of four cell surface receptors; EGF receptor also called as HER1, HER2 or neu, HER3, and HER4. Epithelial growth factor binds to the receptor and stimulates homo/hetero dimerization of receptor with other ERBB member like HER2, receptor phosphorylation, which makes binding sites available for cytosolic proteins containing src homology 2 (SH2) domains [27]. EGFR growth factors cause activation of downstream effectors such as RAS-RAF-MEK-ERK-MAPK and PI3K-AKT-mTOR pathway. PI3K-AKT-mTOR sources irreversible entry of the cell in S phase of cell cycle resulting in cell proliferation [28]. There are various EGFR ligands such as transforming growth factor-α (TGF-α), amphiregulin, epigen, betacellulin, heparin-binding EGF, and epiregulin [29]. EGFR has an important involvement in cellular differentiation, motility, survival, and tissue development [30]. There are many copies of the EGFR gene in some of the breast cancer cells termed as EGFR amplification, which effects on behavior and response of cancer cell. There are other EGFR-positive cancers like colon cancer, which respond to medicines that target EGFR-positive cancers [31]. In a clinical study, there was an increase in EGFR gene copy number in about 6% of breast cancers and protein overexpression in 7% of breast cancers [32]. The study also showed that increased EGFR gene copy number changes, and protein overexpression was seen mostly in ER negative, PR negative, and HER2 negative (triple negative) cases with three exceptions that are HER2-positive cases in total of 175 cases (reference). The study was similar to that of gene expression profiling studies, which have identified EGFR expression mainly in basal-like breast carcinomas (reference). There was another subtype of breast carcinoma that showed an increase in EGFR copy number, or EGFR protein expression is the heterogeneous category of metaplastic carcinoma. These tumors are subtypes called as basal-like breast carcinomas [33] and were seen in 47 metaplastic breast carcinomas in which EGFR protein overexpression was in 32 cases, but gene amplification (as >5 EGFR gene copy number) was seen only in 11 of these 32 (34%) cases [33]. There are other studies that have shown that EGFR gene amplification and EGFR protein overexpression in various organ systems have found similarity in approximately 50% cases [34]. EGFR protein expression is the result of multiple genomic processes of which EGFR gene amplification is only one of them [34]. EGFR protein expression is seen in breast carcinoma, which is mostly triple negative, and there exists a relation between EGFR gene copy number and protein expression, but relation is not as strong as seen with HER2 [34]. The therapeutic use of EGFR as a responsive marker in breast carcinoma is being studied and needs to identify breast cancer patients that will respond to EGFR-related therapies. A new mechanism-based inhibitors and combination therapies are being worked to overcome therapeutic resistance in tumors [34, 35, 36].
3.2 HER2
HER2 gene is amplified in breast cancers by about 20% categorized as HER2-positive breast cancers [37], the extra HER2 protein leads to increase in activation of signal pathway, which results in uncontrolled growth and occurrence of cancer. Breast tumors having HER2 overexpressed proteins are more aggressive than other breast tumors [37]. This results in poorer prognosis in patients and decreased survival rate compared with patients whose tumors do not overexpress HER2 [37]. The inhibition of HER2 signaling will provide a tool to reduce breast cancer. Monoclonal antibodies like lapatinib are used to inhibit the signaling [37]. Herceptin (trastuzumab) is also a monoclonal antibody binding to HER2 [37]. This stops receptor from activating the signaling pathways, which is responsible for proliferation and survival of breast cancer cells [37]. Herceptin also causes inhibition of cancer cell growth by activating an immune response, which will damage nearby cells [37]. It is used to treat breast cancer only in tumor overexpressing HER2 with at least one high risk like estrogen receptor or progesterone receptor negative, pathologic tumor size greater than 2 cm, Grades 2–3, age less than 35 years [37]. Herceptin is used in combination with paclitaxel for first-line treatment of HER2-overexpressing metastatic breast cancer [37].
And as a single agent for treatment of HER2-overexpressing breast cancer in patients who have received one or more chemotherapy regimens for metastatic disease [33, 37, 38].
3.3 HSP27
Heat shock protein 27 (HSP27) is the small molecular weight heat shock protein (HSP) family (12–43 kDa). HSP27 and different members of small HSP family possess a conserved c-terminal domain, the α-crystallin domain, which is similar to the vertebrate eye lens α-crystallin [39]. HSP27 was originally characterized in response to heat shock as a protein chaperone making proper refolding of damaged proteins [40]. It has been seen that HSP27 protein also responds to cellular stress such as oxidative stress and chemical stress. HSP27 is a protein, which functions as a protein chaperone, as an antioxidant helps in inhibition of apoptosis and actin cytoskeletal remodeling, regulation of cell development, cell differentiation, and signal transduction [41]. The oligomerization state of HSP27 is due to chaperone activity as the aggregates of large oligomers have high chaperone activity, whereas dimers have no chaperone activity. Large aggregates are formed under heat shock [40]. Hsp27 occurs in all cell types, mostly of muscle cells. It is located mainly not only in the cytosol but also in the perinuclear region, endoplasmic reticulum, and nucleus. It is overexpressed during cell differentiation and development. It has an essential role in the differentiation of tissues [41].
HSP27 functions as an antioxidant during oxidative stress, which lowers the levels of reactive oxygen species (ROS) by increasing the levels of intracellular glutathione and lowering the levels of intracellular iron [40, 42]. During chemical stress, protein acts as an anti-apoptotic agent through mitochondrial-dependent and -independent pathways of apoptosis [43]. During Fas-FasL-mediated apoptosis, HSP27 binds DAXX and stops the binding of Ask1 by DAXX [43]. HSP27 also interplays with Bax and cytochrome c stopping mitochondrial-dependent apoptosis [43]. HSP27 is mostly useful in protection from programmed cell death by inhibition of caspase-dependent apoptosis [43]. The anti-apoptotic properties of HSP27, which occur due to chemical stress, have been useful in chemotherapies such as doxorubicin and gemcitabine [44, 45]. HSP27 regulates actin cytoskeletal dynamics during heat shock and stress conditions, promotes both actin polymerization, and concerts as an actin capping protein. The upregulation of HSP27 is a biomarker acting in some of the disease subsequently, a cell safeguards itself from death or reduces oxidative stress by the help of HSP27 [46].
In vitro studies have shown that HSP27 acts as an ATP-independent chaperone by inhibiting protein aggregation and stabilizing partially denatured proteins, which ensures refolding by the Hsp70-complex [46]. It also preserves the focal contacts fixed at the cell membrane [46]. The main function of Hsp27 is to provide thermo tolerance in vivo, cytoprotection, and support of cell survival under stress conditions [46]. Another function of Hsp27 is the activation of the proteasome. It speeds up the degradation of irreversibly denatured proteins and junk proteins by binding to ubiquitinated proteins and to the 26S proteasome [46]. Hsp27 enhances the activation of the NF-κB pathway that controls a lot of processes, such as cell growth and inflammatory and stress responses [47]. Various reports have confirmed that cytoprotective properties of Hsp27 have been attributed to its ability to modulate reactive oxygen species production and to raise glutathione levels [47]. Hsp27 is known to play a role in the process of cell differentiation [47].
Hsp27 expression is varied in several cells such as Ehrlich ascites cells, embryonic stem cells, normal B cells, B-lymphoma cells, osteoblasts, keratinocytes, and neurons [47]. The upregulation of Hsp27 relates with the rate of phosphorylation and with an increase in large oligomers [48]. It is possible that Hsp27 plays a crucial role in the termination of growth [40].
3.4 HSP27 in breast cancer
Tumor cells show an increase in transcription of heat shock proteins (HSPs) due to loss of p53 functions and increased expression of proto-oncogenes such as HER and c-Myc, which is important for tumorigenesis [49]. Cellular protection and protein folding being the entailed function of HSPs are operative during oncogenesis [49]. Since tumor cell growth and survival are enabled by the increased expression of HSPs. HSP27 is mostly the important heat shock protein involved in protection from programmed cell death by inhibiting caspase-dependent apoptosis [45]. Since HSP27 has been associated with poor prognosis in many types of cancers such as gastric, liver, and prostate carcinoma, osteosarcoma, rectal, lung, and breast cancer [45]. HSP27 has been reported to play an important drug resistance in breast cancer, and some other cancers, HSPs, are involved in immune tolerance by cancer cells and are important targets for cancer therapy process [50]. A study done by Langer et al. in 2008 found that the protein expression profiles in patients with esophageal adenocarcinomas from two groups have shown as responsive and nonresponsive to neo-adjuvant platin and 5-fluorouracil based chemotherapy. The study showed that low HSP27 expression has a correlation with nonresponsiveness to the chemotherapy application [49]. It shows that low levels of HSP27 expression are associated with a negative outcome in cancer. HSP27 levels were studied in patients having colon or rectal cancer [49]. It showed that high HSP27 expression level results in incomplete resection margins in rectal cancer and poor survival.
HSP27 expression was not having any role in survival of colon cancer group but was related to poor survival in the rectal cancer group [49]. The metastatic breast cancer cell lines, which overexpress Her2 and are resistant to Herceptin (SK-BR3 HR), also overexpress HSP27 [49]. The downregulation of HSP27 protein levels was shown by transfecting with siRNA, where Herceptin resistance was also reduced in SK-BR3-HR cells [49]. HSP27 could form a complex with Her2, resulting in a potential mechanism by which the protein potentiates [51]. Her2 overexpressing breast cancer tumors have showed increased expression of phosphorylated HSP27, particularly at serine 78 [51, 52].
3.5 H2AX (H2A histone family, member X)
Histone H2A is programmed by a gene H2AFX (H2A histone family, member X), as H2A is one of the four core histones of DNA in humans and eukaryotes [53]. H2AX helps in nucleosome formation and in the structure of DNA. DNA known as the most stable material present, whose damage occurs due to ionizing radiation, hypoxia, reactive oxygen species, chemicals, and replication or transcriptional errors, which causes activation of DNA repair pathway [53]. Different materials can cause different types of damage in DNA-like double stranded breaks (DSBs), where both DNA strands have been cleaved [53]. If the damage occurred is not repaired, DSBs are lethal for the cell. DNA damage leads to an activation of the DNA damage repair pathway, phosphorylation of histone H2AX on serine 139. Activation of downstream pathway is done by the kinases of the PI3 family (ataxia telangiectasia mutated, ATR, and DNA-PKcs), which are responsible for this phosphorylation, especially ATM. γ-H2AX enrolls other factors, for example, 53BP1, BRCA1, MDC1, and the MRE11-RAD50-NBS1 (MRN) complex to sites of damage [53]. The DSBs, which are not repaired due to irradiation induced γ-H2AX foci, have been used in tumors as a biomarker for sensitivity to radiotherapy [54]. Endogenous γ-H2AX foci are present in normal primary human cells and tissues [54]. In tumor cells, phosphorylated H2AX exists in different levels in the absence of exogenously DSBs [54]. Instability of chromosomes occurs in cells having more endogenous foci [41]. The colocalization of these endogenous foci in association with other DNA repair factors, for example, 53BP1, MRN complex shows that DNA repair occurs at these sites [54]. The endogenous expression of γ-H2AX is present not only in tumor cell lines but also in cancer tissues and in their precursor lesions, which gives an insight into activated DNA damage repair in tumorigenesis [55]. The endogenous expression of DNA damage response factors is also due to damaged, shortened telomeres and hypoxia [56, 57].
Constitutive γ-H2AX expression is higher in triple negative and in BRCA1 and p53-mutated breast cancer cell lines, which makes a relation between endogenous γ-H2AX expression and 53BP1 expression in breast cancer tissue [55]. Other studies have also supported that triple negative breast cancers are having more endogenous γ-H2AX expression and have higher chances of carrying errors in components of the DNA damage repair pathway [55, 57]. Higher occurrence of γ-H2AX positive is present in basal like and triple negative tumors that are BRCA1 mutation carriers. So, the breast cancer patients having high endogenous γ-H2AX or 53BP1 expression showed a subset of triple negative tumors with poor prognosis. The expression of endogenous γ-H2AX in cancers is due to telomeres (protective structures that form the chromosome ends in eukaryotes) [57].
Cell having DNA damaged after duplication of DNA results in shortened telomeres after every cell cycle, so in precancerous event, there occurs shortening of telomeres and activation of telomerase, an enzyme necessary for telomere lengthening [58]. Telomere shortening in normal process is an action for replication arrest and replicative senescence, but in the absence of a telomeric structure, chromosome ends are not stable and are likely either to undergo degradation, combining with other chromosomes resulting in genomic instability or having DNA double-stranded breaks [58]. A good number of endogenous γ-H2AX foci present, which do not have actual double-stranded breaks, are in fact uncapped telomeres, but the DNA damage and phosphorylation of H2AX at these sites occur due to nonfunctioning of telomere [58]. Telomere-associated chromosomal rearrangements may lead to a tumor phenotype with the associated immortality and replicative potential without any barrier [58, 59].
4. PARP poly ADP ribose polymerase
4.1 PARP in normal cells
PARP1 (protein) repairs single-strand breaks of DNA in a normal cell when it is damaged or mutated, and the cell survives when its DNA repaired, but sometimes when the DNA repair mechanism fails, the cell undergoes suicidal apoptotic process, subsequently that the damaged DNA is not passed to progeny cells [60]. When DNA is damaged or requires repair, one of the proteins, which is involved in repairing damaged DNA, is poly (ADP ribose) polymerase 1, or PARP1 moves at the site of damage, gets activated, and enables various DNA repair proteins to repair the broken strand of DNA, but if the breaks in DNA are not repaired until DNA replication occurs, then the replication itself causes double-strand breaks to form [60]. Inhibition of PARP1 is done by number of drugs, which causes double-strand breaks. Tumors having BRCA1, BRCA2, or PALB2 mutations where repair is not done, the double-strand breaks cannot be repaired causing death of cells [61]. In normal cells, DNA replication is not as frequent as in cancer cells, and they also do not have mutated BRCA1 or BRCA2 but have homologous repair mechanism, which makes them to survive the inhibition of PARP [61]. There are cancer cells that lack the tumor suppressor PTEN and maybe sensitive to PARP inhibitors because of downregulation of Rad51, a critical homologous recombination component [33]. A study has shown that PARP inhibitors may also be effective against PTEN-defective tumors like prostate cancers. Most of the tumors are sensitive to PARP inhibitors [61].
4.2 PARP in breast cancer cells
DNA damage in dividing cells or tumor cells is caused mainly by the chemotherapeutic drugs and radiation therapy, but if PARP repairs the damage caused by these agents, the tumor cells survive and grow.
4.3 Inhibiting PARP: mechanism of action
The preclinical studies have shown that standard therapies alone are not as effective as in combination with PARP inhibitors; they are used in cancer cells, which make protein unable to function during chemotherapy, which results in apoptosis of the cell where DNA is unrepaired [61]. In inherent DNA repair defects, such as breast tumors with mutations in the DNA repair proteins BRCA1 or BRCA2, PARP inhibitors are effective as single agents, and they undergo an arrest of the cell cycle and apoptosis on exposure to PARP inhibitors, whereas cells with normal BRCA proteins survive and continue to grow [61]. It has also been predicted that cancer cells with BRCA1 or BRCA mutations are more sensitive to PARP inhibitors to undergo growth arrest and apoptosis than cells with normal BRCA1 or BRCA2 [61]. This occurs due to combination of PARP and loss of BRCA1 or BRCA2 function causing inactivation of two major forms of DNA repair [61], and the damaged cells are not able to maintain the integrity of their genome and become more prone to apoptosis [37, 38, 62].
Function of PARP inhibitors is to block PARP enzyme activity, which stops the repair of DNA damage and causes the cell death [62]. In one of a clinical study that has shown the PARP inhibitors localize PARP proteins near the site of DNA damage, which suggests its role in antitumor activity [62]. The PARP inhibitors are able to trap PARP proteins on damaged DNA, and this function varies among inhibitors, for example, PARP family of proteins in humans includes PARP1 and PARP2, which are used in binding of DNA and protein repair action [63]. DNA damage causes activation of these proteins; they recruit other proteins that are actually involved in repairing DNA [63]. In normal condition, PARP1 and PARP2 are released from DNA when the repair mechanism is in process [64]. The study shows that when they are attached to PARP inhibitors, PARP1 and PARP2 become trapped on DNA [38]. The trapped PARP-DNA complexes are more harmful to cells than the single-strand DNA breaks, which are not repaired that accumulate in the absence of PARP activity resulting in harmful action of PARP inhibitors [38, 62]. There may be two classes of PARP inhibitors, catalytic inhibitors that block PARP enzyme activity and do not trap PARP proteins on DNA and dual inhibitors that both inhibit PARP enzyme activity and act as PARP poison [38, 63, 64]. Various PARP inhibitors are used in clinical trials as shown in Table 1.
A number of studies have been done to see the toxicity with PARP inhibitors as monotherapy in tumors with homologous recombination defects and have been compared with chemotherapy [68]. Moreover, in some studies, combination of PARP inhibitors is used in combination with chemotherapy. PARP inhibitors as known can act as chemo sensitizing agents [68]. The resistance to chemotherapy drugs occurs when PARP repairs the DNA damage caused by these agents, for example, temozolomide is an alkylating agent, which causes DNA damage in which PARP inhibitors act as potential anticancer agents [68].
4.5 PARP in combination with radiotherapy
Radiotherapy causes DNA strand breaks leading to DNA damage and cell death; however, it kills all of the targeted cells, having side effects [68]. Combining radiation therapy with PARP inhibitors has been used to overcome the side effects as these inhibitors form double-strand breaks from the single-strand breaks generated by the radiotherapy in tumor tissue with BRCA1 or BRCA2 mutations. In such cases, the combinatorial therapy leads to better and efficient response with less dose of radiation [68].
5. ROS
Reactive oxygen species (ROS) are reactive molecules containing oxygen [69]. These molecules are formed when a chemical reaction takes place, for example, between oxygen ions and peroxides [69]. ROS plays an important role in cell signaling and homeostasis, due to environmental stress like UV or heat exposure, and ROS levels are increased, which damage cell structure and its function [69].
5.1 ROS in cancer
ROS being secondary messengers in cell signaling are required for various biological processes in normal cells; any dysfunction in redox balance results in human cancers [27]. ROS are increased mostly in cancer cells when oncogenes are activated, and there is lack of blood supply, which initiates progression and metastasis of cancer [27]. ROS levels decide the difference between tumor and nontumor cells [27]. Generation and elimination of ROS at the same time in the system are the expenditure to operate regulatory pathways in a normal physiological condition of cell, and this process is balanced by scavenging system [27]. When oxidative stress occurs, ROS are generated more, which cause carboxylation of cellular proteins, peroxidation of lipids, and DNA damage leading to dysfunction of cell resulting in carcinogenesis, while in cancer cells, ROS stress causes increased metabolism and mitochondrial dysfunction [27]. Consequently, ROS have dual function, on one side, it helps in survival of cancer cell, as cell cycle progression, which is regulated by growth factors via receptor tyrosine kinase activation and chronic inflammation, is regulated by ROS [62]. On an altered side, an increase in ROS level suppresses tumor growth by activating cell cycle inhibitors, which induces cell death and senescence by damaging macromolecules [62]. This dual mechanism helps in chemotherapy and radiotherapy, where cancer cells are killed by ROS stress. The cancer cells are able to differentiate between ROS as survival or apoptotic signal because of the dosage, duration, type, and site of ROS production [66]. ROS is used for survival of cancer cells in moderate level and kills cancer cells in excessive level [66]. Effects of ROS are maintained by cell metabolism by producing antioxidant molecules such as reduced glutathione (GSH) and thioredoxin (TRX), which depend on the reducing power of NADPH to maintain their function (reference) [27]. Sometimes tumor cells overproduce ROS because the NADPH oxidase is regulated by the GTPase Rac1, which is a downstream of proto-oncogene Ras [27]. ROS when associated with cancer activate various transcription factors such as nuclear factor kappa-light-chain-enhancer of activated B cells—NF-κB, activator protein-1—AP-1, hypoxia-inducible factor-1α, and signal transducer and activator of transcription 3—STAT3, which cause protein expression for inflammation, cell transformation, tumor cell survival and proliferation and invasion, angiogenesis, and metastasis (reference). ROS also control the expression of different tumor suppressor genes such as p53, retinoblastoma gene (Rb), and phosphatase and tensin homolog (PTEN) [70, 71, 72, 73].
The several causes for oxidative stress in breast cancer cells are as follows:
Thymidine phosphorylase induction in cancer cells is caused by oxidative stress, an enzyme that is overexpressed in breast cancer. Thymidine phosphorylase catabolizes thymidine to thymine and 2-deoxy-D-ribose-1-phosphate, which is a very powerful reducing sugar that rapidly glycates proteins, generating oxygen radicals within the cancer cell [74].
Glucose deprivation and hypoxia is caused by continuously usage of blood supply which causes increased cellular oxidative stress in MCF-7 breast cancer cell line but does not increase in nontransformed cell line, reason being glucose deprivation depletes intracellular pyruvate in breast cancer cell, which prevents the decomposition of endogenous oxygen radicals [75]. Study done [76] supports that breast tumor increases its blood supply, leading to glucose deprivation and hypoxia thus causing glucose deprivation, which rapidly induces cellular oxidative stress within the MCF-7 breast carcinoma cell line, although it does not cause oxidative stress in nontransformed cell lines [75]. Cancer cells like breast cancer cells cause increase in blood vessel development (angiogenesis process), where blood flow causes hypoxia followed by reperfusion, which leads to myocardial infarction leading to generation of ROS which leads to oxidative stress in breast cancer [75].
Breast tumors are accompanied by macrophage population [75]. Oxygen radicals are produced by macrophages; it causes oxidative stress in murine mammary tumor cells. Also, tumor necrosis factor is secreted by macrophages, which also cause cellular oxidative stress [67, 77].
5.2 Effects of ROS in breast cancer
Increase in mutation rate and tumor progression is caused mainly by ROS in which oxygen radicals cause DNA damage, which result in strand breaks, alterations in guanine and thymine bases, and sister chromatid exchanges [78]. ROS lead to inactivation of tumor suppressor genes in tumor cells and increase expression of proto-oncogenes; thus, genetic instability due to persistent oxidative stress in cancer cell will increase malignancy of the tumor [79]. In vitro ROS cause initiation of growth sensing signaling pathways due to cell proliferation in response to hydrogen peroxide because of activation of mitogen-activated protein kinases (MAPKs), like HeLa cells when treated with hydrogen peroxide lead to activation of all three MAPK pathways, extracellular signal-related protein kinase, c-Jun amino-terminal kinase, and stress-activated protein kinase and p38 [79]. Hyper-phosphorylation of c-Jun by oxidative stress activates activator protein-1 in MCF-7 breast cancer cells, which stimulates proliferation [80]. Multidrug-resistant human breast carcinoma cells lead to activation of extracellular signal-related protein kinase-2 when stressed by glucose deprivation [76]. ROS may also cause stimulation of mitosis by MAPK-independent mechanisms. Oncogenic Ras causes ROS production by activating Rac1 and NADPH-oxidase. It has been also seen that in Ras-transformed human fibroblasts, ROS control cell cycle progression without the activation of MAPK pathways [81, 82].
5.3 Resistance to therapy
Apoptosis is caused by oxidative stress, which is induced depending on p53 in both mouse and human cells [83]. Resistance to apoptosis is caused by persistent oxidative stress [84], whereas the resistant to cytolysis by hydrogen peroxide may be explained by an upregulation of anti-ROS mechanism in cancer cells. Hydrogen peroxide activates anti-apoptotic Akt (protein kinase B) leading response to chronic oxidative stress that can be used for anticancer therapy though in radiotherapy, photodynamic therapy, and other chemotherapies generating oxygen radicals showing antitumor activity [85]. This is due to the induction of tumor cell apoptosis in response to oxidative stress and oxygen radical prompted DNA damage [85]. This results in persistent oxidative stress within carcinoma cells causes resistance to therapy that is further increased by oxygen radicals leading to an increasing carcinoma cell expression of P-glycoprotein, the multidrug-resistance efflux pump [86].
Angiogenesis, which may be one of the reasons for oxidative stress, leads to tumor growth in blood borne metastasis of breast tumor, where oxygen radicals cause tumor migration causing increased risk of invasion and metastasis by activation of p38 MAPK and subsequent phosphorylation of heat shock protein-27 by p38 MAPK causing changes in actin dynamics [46, 79]. Studies have shown that phosphorylated heat shock protein-27 promotes the migration of MDA-MB-231 breast cancer cells on laminin-5 in vitro [41]. Oxidative stress in breast tumors causes invasion and metastasis by activating MMPs as well as by inhibiting antiproteases. MMP-2 as gelatinase has a major role in breast cancer invasion and metastasis; once its levels are high, there is a poor prognosis in breast cancer patients [87]. Subsequently, MMP-2 is seen more in malignant than in benign breast tumors; therefore, it is ROS, which also activate MMP-2 due to reaction of oxygen radicals with thiol groups within MMP-2 [88]. Oxygen radicals inactivate protease inhibitors, such as α1-proteinase inhibitor and plasminogen activator by oxidation of methionine residues at their active sites [65], leading to protease activation, which increase invasion and metastasis processes, for example, plasminogen activator causes metastasis [65].
Cancer cells synthesizing ROS at a higher level in vitro and tumors in vivo are under persistent oxidative stress, as oxygen radicals lead to a poorer prognosis, antioxidants can be used for therapeutic role in breast cancer [89]. Various research studies have shown that human melanoma cells were transfected with cDNA encoding the antioxidant enzyme manganese superoxide dismutase leading to suppression of malignancy; cells not only lost their ability to form colonies on soft agar but also no longer formed tumors in nude mice [89]. Various anticancer therapies are there, which add to the oxidative stress within breast cancer such as chemotherapeutic agent’s doxorubicin, mitomycin C, etoposide, and cisplatin, which are superoxide generating agents [85], radiotherapy, and photodynamic therapy, which generate oxygen radicals within the carcinoma cell, and anti-estrogen tamoxifen used in breast cancer therapy also induces oxidative stress within cancer cells in vitro [90]. Conversion of breast tumors to a tamoxifen-resistant phenotype that has been seen is associated with a progressive shift toward a pro-oxidant environment of cells as a result of oxidative stress [90].
6. P53
P53 protein, a tumor protein present in humans, which is encoded by the TP53 gene (tumor suppressor gene), functions to inhibit proliferation of cells and regulates cell cycle, thereby preventing cancer, also called as the guardian of the genome as it maintains the stability in a cellular process preventing genetic mutation, under normal cellular phenomenon the p53 signaling pathway is in static mode, whereas its activation occurs when there is a cellular stresses like DNA damage or oncogene activation [91, 92]. Post-translational modifications activate P53 protein for DNA binding, transactivating downstream effector genes whose activation depends on the nature of stress and its extent. After oxidative stress transcriptional coactivators, for example, apoptosis stimulating protein of p53 and BRCA1 promotes various cellular processes like apoptosis, other components of signaling pathway which are targeted for genetic and epigenetic changes in breast cancer, for example, activation of MDM2 which acts as a negative feedback regulator of the pathway by promoting the degradation of p53 [93].
6.1 P53 mutations in breast cancer
p53 being activator of apoptosis or cell cycle arrest is generated upon DNA damage, or cellular stress has a major role in cancer as it stimulates genomic stability and anti-angiogenic effects, manages tumor inflammation and immune response, and represses metastases [94]. TP53 is mutated mostly in 50% of all human cancers and in 20–30% of breast cancers with more than 15,000 different mutations, which makes P53 as a potential biomarker for breast cancer [94].
In one of a clinical study, it was studied that in premenopausal women, p53 mutation is associated with ER and PR tumors, but in postmenopausal women having breast cancer, the presence of a p53 mutation is associated with higher body mass index (BMI), higher-grade, and poorly differentiated tumors, so women having tumors as well as p53 mutations had a 2.4-fold increased risk of dying from their disease [53]. In an additional clinical study, it has been shown that TP53 mutated noninflammatory locally advanced breast carcinomas respond to doxorubicin-cyclophosphamide chemotherapy unlike TP53 wild-type tumors, due to senescence in TP53 wild-type tumor cell and in MMTV-Wnt1 mammary tumors, growth arrest and senescent phenotype were stimulated in TP53 WT tumors following doxorubicin treatment, and there was no apoptosis while the absence of arrest in mutant tumors caused aberrant mitosis, cell death, and a better clinical response [53, 95]. In ER-positive breast tumors, ER represses the p53-mediated apoptotic response induced by DNA damage, but in ER-negative TP53 mutated breast cancers, accumulation of genetic abnormalities may lead to mitotic catastrophe and better response [95].
6.2 P53 and chemotherapy
Previous clinical studies done on breast cancer patients [96] have seen that ER (+) tumors (mostly TP53 wild type) are mostly resistant to chemotherapy, while ER (−) tumors (mostly a TP53 mutated) are more chemo sensitive, but in another study, it was found that there was no association shown in sensitivity to classical doses of taxane-based therapy and mutated TP53 in breast tumor [97]. TP53 wild-type tumor cells in human breast xenograft models have the presence of senescence in breast cancers in response to the treatment [95] senescence induction and cell cycle arrest in TP53 wild type tumors showed tumor proliferation after the end of treatment while genetic abnormalities and mitotic catastrophe would occur with further response to treatment in TP53 mutated tumors, which was also seen in MMTV-Wnt1 mammary tumors [95]. It has also been seen that growth arrest and senescent phenotype and no apoptosis were induced in TP53 wild-type tumors following doxorubicin treatment, while lack of arrest in R-172-H mutant tumors resulted in aberrant mitoses, cell death, and a better clinical response; wild-type tumors or mutant tumors, which were having a wild-type TP53 allele, did not show apoptosis and did not lose any volume as did TP53 mutant tumors [98]. In ER (+) breast cancers, it was shown that there is a functional interplay between p53 and ER on a genome wide scale and that ER represses the p53-mediated apoptotic response induced by DNA damage, and distinct TP53 gene signatures are also needed to evaluate prognosis and response to chemotherapy in ER-positive and ER-negative breast cancers [74].
Thus, these clinical findings provide a way how to study p53-mediated response to dose-dense doxorubicin-cyclophosphamide chemotherapy in breast carcinomas in ER (+) TP53 wild-type breast tumors and that ER-induced inhibition of p53 apoptotic response would result in tumor cell senescence and resistance to treatment. However, in ER (−) TP53 mutated breast carcinomas, mostly in those having lost both TP53 alleles, there is an increase in genetic abnormalities that lead to mitotic catastrophe and better response [74].
6.3 P53 and ROS signaling
p53, a tumor suppressor protein being redox active transcription factor, organizes and directs cell function during various stresses that lead to genomic instability, on the other hand, reactive oxygen species (ROS) are products or byproducts generated by cells, which function either as signaling molecules or as cell toxicants (reference). Cellular concentration and distribution of p53 have a different cellular function as ROS act as both up-stream signal that causes p53 activation and downstream factor that results in apoptosis [99], subsequently if ROS level is increased due to oxidative stress in cancer cell, then p53 level may be increased to maintain its stability in the environment [99]. A balance is maintained in cellular concentration between oxidant and antioxidant molecules in normal cells, but when the oxidant part increases or when a disruption of redox signaling occurs, oxidative stress is caused in a redox reaction in the system, which results in damage to DNA, proteins, and lipids through oxidative modification resulting in number of diseases and chemotherapeutic cytotoxicity [15].
The genomic stability is maintained by tumor suppressor protein p53, but when there is a cellular stress like disruption of redox signals, which leads to damage DNA, proteins, and lipids. This tumor suppressor gene maintains transcription of various genes and directs cell for cell cycle arrest, senescence or apoptosis through various activation of target genes, many effector molecules like proteins, noncoding RNAs, for example, myc, Hcas or CSE1L, Hzf and miR-34 which help in selecting transactivation of p53 target genes leading to various cellular responses comes into play [85]. Thus, this oxidative stress is associated with p53-dependent cell cycle arrest, DNA repair, and apoptosis, but a clear understanding of the mechanisms of the interactions between ROS and p53 is still elusive [100].
In unstressed cell or normal cell, P53 has a small half-life and is present in low levels by continuous ubiquitination by Mdm2 COP1 (constitutively photomorphogenic 1) and Pirh2 (p53-induced protein with a RING-H2 domain) and derogation by 26S proteasome, where the physiological levels of p53 have different effects on cellular redox potential either it regulates the pro-oxidant and antioxidant genes or it modulates the cellular metabolism [86, 101].
6.4 Levels of p53 and ROS
Overexpression of p53 transactivates a series of p53-induced genes (PIGs) in which many of these PIGs encode redox active proteins including two ROS-generating enzymes, NQO1-quinone oxido-reductase, PIG3, and proline oxidase (POX, PIG6). The upregulation of these pro-oxidant enzymes will lead to oxidative stress and apoptosis [102, 103]. The pro-oxidant genes, which are upregulated, are BAX, PUMA, and p66shc in which BAX and PUMA stimulate uncoupling of mitochondria, which result in ROS generation from a less efficient electron transport chain, and P66shc is a downstream target of p53, which is present in cytoplasm and is translocated into mitochondria by prolyl isomerase 1 (Pin1) and mitochondrial heat shock protein (mtHsp 70), and pro-apoptotic stimulation of p66shc oxidizes cytochrome c, which produces H2O2 and opens mitochondrial permeability transition pore initiating apoptosis, and upregulation of these pro-oxidant enzymes leads to oxidative stress and consequently to apoptosis [102, 103]. More genes have been added to the list of p53-induced pro-oxidant genes, which include BAX, PUMA, and p66Shc of which BAX and PUMA can induce uncoupling of mitochondria, resulting in ROS being generated from a less efficient electron transport chain (ETC) [74, 104]. P53 has a downstream target known as p66Shc, which predominantly exists in cytoplasm and is translocated into mitochondria with the help of prolyl isomerase 1 (Pin1) and mitochondrial heat shock protein 70 (mtHsp 70) [105, 106].
Oxidative stress is caused by suppression of antioxidant genes by p53, which increases cellular ROS, for example, MnSOD (manganese superoxide dismutase) is suppressed at the promoter level by p53 activation or overexpression [107].
6.5 Redox regulation of p53
The oxidative stress caused by ROS is related to various p53-mediated cell processes like cell cycle arrest, DNA repair, and apoptosis like increase in generation of ROS in mitochondria when treated with chemotherapeutic agent’s results in apoptosis, while oxidative stress in the nucleus causes cells to p53-dependent DNA repair [86, 92]. A number of pathways operating to induce redox and p53 signaling select various p53 target genes that decide the final fate of the cell have been found significant in studies going on cisplatin and ginkgo bilobalide resulted in chemotherapeutics-induced ROS increase C-myc [108]. As soon as C-myc levels increase, it causes suppression of p53 transactivation of p21Cip1 blocking cell cycle arrest but does not affect p53-transactivation of the pro-apoptosis gene PUMA leading to apoptosis [108]. The mechanism acts in a same manner as in pathogenic bacterium Pseudomonas aeruginosa induced cell death having azurin, a copper-containing redox protein excreted by Pseudomonas aeruginosa that binds to p53 and transactivates pro-apoptosis protein Bax resulting in apoptosis [108].
6.6 Redox modification
p53-mediated ROS generation is the most important cellular concentration and subcellular localization function as P53 is a redox sensitive protein, which undergoes redox modification and decides the cell fate on the basis of p53 target genes, and the other factors such as cell type, stress, and intensity of stimuli give an insight into the interaction between ROS and p53 [92, 95].
7. P38-MAP kinase
Response to extracellular stimuli is managed and regulated by intracellular signaling pathways by mitogen-activated protein (MAP) kinase pathways whose members are responsible for signaling cascades, mammalian p38s responses, inflammatory cytokines (TNF-& IL-1), growth factors (CSF-1), ultraviolet irradiation, heat shock, osmotic shock, function in cell differentiation, apoptosis, and autophagy [109]. In general, there are four MAP kinase family subgroups, namely extracellular signal-regulated kinases (ERKs), c-jun N-terminal or stress-activated protein kinases (JNK/SAPK), ERK/big MAP kinase 1 (BMK1), and the p38 group of protein kinases [110]. p38 (p38), a 38-kDa protein when phosphorylated by tyrosine as a responsive protein to LPS stimulation (Han et al. 1993) and its kinases are divided by Thr-Gly-Tyr (TGY) dual phosphorylation motif residues in a TXY (where X is Glu, Pro and Gly in ERKs, JNKs and p38 MAPKs) activation motif by a dual specificity, activation of p38 is not only due to responsive nature on stimulus, but on cell type as well., Insulin signaling is reported to activate p38 in 3T3-L1 adipocytes but downregulates p38 in chick forebrain neuron cells [110].
7.1 p38 in the cell cycle
p38 has been studied in G1, G2, and M phases of the cell cycle [30]. p38 MAPK controls both the G2/M and G1/S cell cycle checkpoint in retort to cellular stress corresponding to DNA damage [30]. It facilitates the cell survival processes and initiation/maintenance of cell cycle checkpoints in retort to particular stimuli [30].
7.2 p38 in senescence and tumor suppression
A number of studies have provided evidence of p38 role in tumorigenesis and senescence [28], when there is a loss of senescence in tumor cells, it has been found that its activation may be decreased in tumors and that its pathway units such as MKK3 and MKK6 are lost resulting in increased proliferation [111].
7.3 p38 role in breast cancer
p38 MAPK in survival of tumor cells functions independently of DNA damage and supplements to metastasis, but this effect is indirectly regulated by p38 MAPK through the mediation of factors responsible for survival or migration of cells, for example, basal stimulation of p38 MAPK in B-cell chronic lymphocytic leukemia (B-CLL) is required for the MMP-9 metalloprotease for survival of these cells grown in the presence of stroma cells [112]. However, in vivo studies found that the decreased basal as well as TGFβ1-induced MMP-9 activity in breast cancer cells cause inhibition of p38 MAPK pathway by genetic regulators and pharmacological compounds causing decreased bone metastases [113].
In cell division and cell survival, p38 is studied at checkpoint control [113]. Role of p38 in invasiveness in cultured cell has been seen, which shows that phospho-p38 level is increased in cultured invasive breast cancer cells [95, 114]; increased expression of P38 MAPK in breast cancer has been found in relation to poor prognosis and in invasiveness and metastasis [115]. Overexpression of phosphorylated-P38 MAPK has been seen in ~20% of primary breast carcinomas or in relation to HER2 amplification and tamoxifen resistance and is a potential prognostic marker in breast cancer [116]. Therefore, the role of P38 MAPK in breast cancer cell proliferation remains a subject of study as it has dual function in survival and proliferation depending on the expression of mutant TP53 being present in most ER-breast tumors to develop P38 MAPK inhibitors for the treatment of TP53-mutated, ER-breast cancers, it is expressed at a higher level in ER+ in comparison with ER tumors without post-transductional activation as there was no change in the phosphorylation rate of P38 MAPK [116].
8. Role of tamoxifen resistance in breast cancer
A number of studies have reported the role of P38 MAPK in the resistance of ER+ breast tumors to endocrine therapy [117] and its relation between activated P38 MAPK levels and tamoxifen resistance [114, 118]. It has been reported that P38 MAPK leads to increased ER agonist activity through increased phosphorylation of ER and increased ER signaling through coactivator regulation [76]. There is switch in estrogen receptor signaling from its classical pathway to the AP1-dependent nonclassical pathway upon activation of MAPK by anti-estrogens apart from ER being their main target; thus, the activation of P38 MAPK can reduce the cellular response to endocrine therapy, which has been reported as a biomarker for resistance to endocrine therapy, and its detailed study of expression and its activation in breast tumors may provide a new approach to the resistance of breast cancer to endocrine therapy; also it has been reported that increased phospho-p38 levels have been associated with high expression of EGFR and ErbB2 in tamoxifen-resistant xenografts, where it acts to support nuclear functions of ER [76]. In matched primary and recurrent tamoxifen-resistant tumors (and a parallel study of a mouse xenograft in tamoxifen resistance), a link between phospho-p38 and increased ErbB2 with tamoxifen resistance was found [64, 69, 119, 120]. The graphic illustration of the pathway is displayed in Figure 1.
Figure 1.
Signalling pathway affecting estrogen receptor (ER) causing increase in EGFR level leading to cell proliferation during tamoxifen resistivity. P53 is increased during resistance and controls p21 function as well. ROS level is increased causing cell proliferation which in turn decreases Hsp27 and MAPK-P38 activity during stress lead by tamoxifen resistance.
Acknowledgments
The authors acknowledge Sheri Kashmir Institute of Medical Sciences for academic support.
Conflict of interest
The authors declare no conflict of interest.
\n',keywords:"cell cycle, breast cancer, drug resistance, tumor suppressor genes, oncogenes",chapterPDFUrl:"https://cdn.intechopen.com/pdfs/72259.pdf",chapterXML:"https://mts.intechopen.com/source/xml/72259.xml",downloadPdfUrl:"/chapter/pdf-download/72259",previewPdfUrl:"/chapter/pdf-preview/72259",totalDownloads:243,totalViews:0,totalCrossrefCites:0,dateSubmitted:"January 8th 2020",dateReviewed:"April 16th 2020",datePrePublished:"May 20th 2020",datePublished:null,dateFinished:null,readingETA:"0",abstract:"Cell cycle progression is driven by the sequential activation of a family of cyclin-dependent kinases (CDKs), which phosphorylate and activate proteins that execute events critical to cell cycle progression. Cell cycle checkpoints are scrutiny points that display the order, integrity, and fidelity of the major proceedings of the cell cycle. These comprise development to the correct cell size, the replication, integrity of the chromosomes, and their precise separation at mitosis. Many of these mechanisms are prehistoric in origin and highly preserved and hence have been deeply well versed by studies in model organisms such as the yeasts as well as in higher organisms. These molecular mechanisms switch alternative cell fates with substantial impact on tumor suppression. In the present study, we have explained different checkpoint pathways and the consequences of their dysfunction on cell fate in cancer.",reviewType:"peer-reviewed",bibtexUrl:"/chapter/bibtex/72259",risUrl:"/chapter/ris/72259",signatures:"Shazia Ali, Mohd Ishaq Dar, Rafiq A. Rather and Dil Afroze",book:{id:"8207",title:"Breast Cancer Biology",subtitle:null,fullTitle:"Breast Cancer Biology",slug:"breast-cancer-biology",publishedDate:"July 8th 2020",bookSignature:"Dil Afroze, Bilal Rah, Shazia Ali, Faheem Shehjar, Mohd Ishaq Dar, Shailender S. Chauhan and Natasha Thakur",coverURL:"https://cdn.intechopen.com/books/images_new/8207.jpg",licenceType:"CC BY 3.0",editedByType:"Edited by",editors:[{id:"244441",title:"Prof.",name:"Dil",middleName:null,surname:"Afroze",slug:"dil-afroze",fullName:"Dil Afroze"}],productType:{id:"1",title:"Edited Volume",chapterContentType:"chapter",authoredCaption:"Edited by"}},authors:[{id:"244441",title:"Prof.",name:"Dil",middleName:null,surname:"Afroze",fullName:"Dil Afroze",slug:"dil-afroze",email:"afrozedil@gmail.com",position:null,institution:{name:"Sher-i-Kashmir Institute of Medical Sciences",institutionURL:null,country:{name:"India"}}},{id:"249300",title:"Dr.",name:"Shazia",middleName:null,surname:"Ali",fullName:"Shazia Ali",slug:"shazia-ali",email:"w.shazia@gmail.com",position:null,institution:null}],sections:[{id:"sec_1",title:"1. Introduction",level:"1"},{id:"sec_2",title:"2. Drug resistance",level:"1"},{id:"sec_2_2",title:"2.1 Cell cycle regulation in tamoxifen-resistant breast cancers",level:"2"},{id:"sec_4",title:"3. Genes associated with breast cancer development and its progression",level:"1"},{id:"sec_4_2",title:"3.1 EGFR",level:"2"},{id:"sec_5_2",title:"3.2 HER2",level:"2"},{id:"sec_6_2",title:"3.3 HSP27",level:"2"},{id:"sec_7_2",title:"3.4 HSP27 in breast cancer",level:"2"},{id:"sec_8_2",title:"3.5 H2AX (H2A histone family, member X)",level:"2"},{id:"sec_10",title:"4. PARP poly ADP ribose polymerase",level:"1"},{id:"sec_10_2",title:"4.1 PARP in normal cells",level:"2"},{id:"sec_11_2",title:"4.2 PARP in breast cancer cells",level:"2"},{id:"sec_12_2",title:"4.3 Inhibiting PARP: mechanism of action",level:"2"},{id:"sec_13_2",title:"4.4 PARP in combination with chemotherapy",level:"2"},{id:"sec_14_2",title:"4.5 PARP in combination with radiotherapy",level:"2"},{id:"sec_16",title:"5. ROS",level:"1"},{id:"sec_16_2",title:"5.1 ROS in cancer",level:"2"},{id:"sec_17_2",title:"5.2 Effects of ROS in breast cancer",level:"2"},{id:"sec_18_2",title:"5.3 Resistance to therapy",level:"2"},{id:"sec_20",title:"6. P53",level:"1"},{id:"sec_20_2",title:"6.1 P53 mutations in breast cancer",level:"2"},{id:"sec_21_2",title:"6.2 P53 and chemotherapy",level:"2"},{id:"sec_22_2",title:"6.3 P53 and ROS signaling",level:"2"},{id:"sec_23_2",title:"6.4 Levels of p53 and ROS",level:"2"},{id:"sec_24_2",title:"6.5 Redox regulation of p53",level:"2"},{id:"sec_25_2",title:"6.6 Redox modification",level:"2"},{id:"sec_27",title:"7. P38-MAP kinase",level:"1"},{id:"sec_27_2",title:"7.1 p38 in the cell cycle",level:"2"},{id:"sec_28_2",title:"7.2 p38 in senescence and tumor suppression",level:"2"},{id:"sec_29_2",title:"7.3 p38 role in breast cancer",level:"2"},{id:"sec_31",title:"8. 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Advanced Center for Human Genetics, Sher-i-Kashmir Institute of Medical Sciences, Srinagar, Jammu and Kashmir, India
Advanced Center for Human Genetics, Sher-i-Kashmir Institute of Medical Sciences, Srinagar, Jammu and Kashmir, India
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