Open access

Cripto-1: At the Crossroads of Embryonic Stem Cells and Cancer

Written By

Nadia Pereira Castro, Maria Cristina Rangel, Tadahiro Nagaoka, Hideaki Karasawa, David S. Salomon and Caterina Bianco

Submitted: 22 November 2010 Published: 15 September 2011

DOI: 10.5772/22800

From the Edited Volume

Embryonic Stem Cells - Basic Biology to Bioengineering

Edited by Michael S. Kallos

Chapter metrics overview

3,871 Chapter Downloads

View Full Metrics

1. Introduction

Human Cripto-1 is a member of the Epidermal Growth Factor-Cripto-FRL-1-cryptic (EGF-CFC) family of peptides (Bianco et al., 2010; de Castro et al., 2010). During early vertebrate development, Cripto-1 functions as a co-receptor for transforming growth factor β (TGF-β) ligands, such as Nodal and growth and differentiation factor-1 and -3 (GDF-1 and GDF-3), through an heteromeric complex composed of Activin type II and type I (ALK4) serine threonine kinase receptors in the plasma membrane. Genetic studies in zebrafish and mice have demonstrated that Cripto-1/Nodal signaling is essential for the formation of the primitive streak, patterning of the anterior/posterior (A/P) axis, specification of mesoderm and endoderm and establishment of left/right (L/R)asymmetry(Bianco et al., 2010; de Castro et al., 2010). In adult tissues, Cripto-1 is expressed at low levels in all stages of mammary gland development and its expression increases during pregnancy and lactation. Overexpression of Cripto-1 in mouse mammary epithelial cells leads to their transformation in vitro and can enhance migration, invasion, branching morphogenesis and epithelial to mesenchymal transition (EMT)(Bianco et al., 2010; de Castro et al., 2010). Furthermore, transgenic mouse studies have shown that overexpression of a human Cripto-1 transgene in the mouse mammary gland under the transcriptional control of the mouse mammary tumor virus (MMTV) promoter results in mammary hyperplasias and papillary adenocarcinomas(Wechselberger et al., 2005). Cripto-1 is also expressed at high levels in approximately 50-80% of different types of human carcinomas, including breast, colon, pancreas, lung and ovary(Bianco et al., 2010; de Castro et al., 2010). Cripto-1 is therefore an example of an embryonic gene that plays an important role not only during embryogenesis, but is also implicated in malignant progression. Furthermore, Cripto-1 signaling might represent a common signaling pathway shared by embryonic stem cells and cancer cells. Recent studies have shown that Cripto-1 is an important component of critical core pathways that regulate stem cell self-renewal and differentiation(Hough et al., 2009). Chromatin immunoprecipitation (ChiP) analysis has revealed the presence of Oct-4 and Nanog binding sites in the Cripto-1 promoter region, suggesting that Cripto-1 is a direct transcriptional target of Oct-4 and Nanog transcription factors(Loh et al., 2006). More importantly, several signaling pathways that are critical for early embryonic development and regulate stem cell proliferation and differentiation have been shown to cross-talk with Cripto-1(Bianco et al., 2010). Examples of embryonic signaling pathways that interact with Cripto-1 are the Wnt-β/catenin, the Notch, hypoxia and TGF-β signaling pathways. Interestingly, Cripto-1 and other embryonic genes that regulate stem cell function are also overexpressed in human tumors, confirming this connection between stem cells and cancer. Recently, Cripto-1 has been shown to be highly expressed in a small subset of stem-like cells in human embryonal carcinoma cells, in human malignant melanomas and in androgen-responsive and refractory human prostate cancer cells(Cocciadiferro et al., 2009; Strizzi et al., 2008; Watanabe et al., 2010). Therefore, Cripto-1 signaling pathway may represent an attractive target for treatment in cancer, because Cripto-1 targeting will eliminate not only differentiated cancer cells but also might target an undifferentiated subpopulation of tumor cells that exhibit stem-like characteristics, thereby leading to eradication of the tumor. In this review we will discuss the dual role of Cripto-1 as embryonic gene in the regulation of stem cell self-renewal and differentiation and as oncogene with re-expression in human cancers.


2. The EGF-CFC family

Human Cripto-1 is a member of the EGF-CFC family of peptides identified only in vertebrates, and plays an important role in embryonic development and in tumor progression. The EGF-CFC family includes monkey Cripto-1, mouse Cripto-1 (Cr-1=cfc2), chicken Cripto-1, zebrafish one-eyed pinhead (oep), Xenopus XCR1/FRL-1, XCR2 and XCR3, mouse cryptic (Cfc1) and human Cryptic (CFC1) (Bianco et al., 2005b). Structurally, these proteins contain an NH2-terminal signal peptide, a modified EGF-like domain, a CFC cysteine-rich domain and a short hydrophobic COOH-terminus containing short sequences for glycosylphosphatidylinositol (GPI) cleavage and attachment (Figure 1).

Figure 1.

Structure of the human Cripto-1 protein.

Cripto-1 contains several glycosylation sites and the residue Threonin 88 within the EGF-like domain modulates Cripto-1 ability to activate a Nodal-dependent signaling pathway. Cripto-1 can be cleaved from the cell membrane and can be releasedin the supernatant of cells by activity of the enzyme GPI-phospholipase D(GPI-PLD). EGF: epidermal growth factor, CFC: Cripto-FRL-1-Cryptic, GPI: glycosylphosphatidylinositol, Ser: Serine, Asn: Asparagine, Thr: Threonine.

GPI anchoring determines membrane localization of Cripto-1 within lipid rafts microdomains and is required for the paracrine activity of Cripto-1 as a Nodal co-receptor (Bianco et al., 2008; Watanabe et al., 2007b). Removal of the GPI anchor by GPI-PLD generates a soluble form of Cripto-1, which can therefore function both as a cell membrane anchored protein or as a soluble protein (Watanabe et al., 2007a; Watanabe et al., 2007b). In fact, soluble forms of Cripto-1 are biologically active in a number of different in vitro and in vivo assays (Minchiotti et al., 2001; Xu et al., 1999; Yan et al., 2002). Furthermore, Cripto-1 protein has several glycosyl modification sites, including O-linked glycosylation at Ser40 and Ser161 (-site for GPI-attachment), N-linked glycosylation at Asn79 and O-linked fucosylation at Thr88 (Figure 1) (Minchiotti et al., 2000; Schiffer et al., 2001; Shi et al., 2007; Watanabe et al., 2007a; Watanabe et al., 2007b). Among them, O-linked fucosylation of EGF-CFC proteins is required for their ability to function as co-receptors for the TGF--related protein Nodal (Schiffer et al., 2001). However, Cripto-1 O-fucosylation mutants are fully functional with regard to activation of Nodal independent signaling pathways (Bianco et al., 2008). Another study has demonstrated that is the Thr88 residue and not fucosylation of this residue that is necessary for Cripto-1 to function as a Nodal co-receptor (Schiffer et al., 2001; Shi et al., 2007).


3. Cripto-1 during embryonic development

In the embryonic development EGF-CFC proteins function as co-receptors for the TGF- ligands Nodal, GDF-1 and GDF-3 (Bianco et al., 2010; de Castro et al., 2010 as cited in Yeo et al. 2001; Andersson at al. 2007). Genetic studies in zebrafish and mice have defined an essential role for Nodal that functions through oep/Cripto-1 in the formation of the primitive streak, patterning of the A/P axis, and specification of mesoderm and endoderm (mesoendoderm) (Bianco et al., 2010; de Castro et al., 2010 as cited in Chu et al. 2005). In later stages of embryonic development the EGF-CFC ortholog of Cripto-1, Cryptic, regulates the establishment of L/R axis, allowing asymmetricdevelopment of visceral organs (Bianco et al., 2010 as cited in Yan et al., 1999). Biochemical studies have demonstrated that EGF-CFC proteins bind directly to Nodal, GDF-1 or GDF-3 and the Activin type I receptor ALK4 (ActRIB), recruiting the Activin type II receptor and inducing activation and phosphorylation of Smad-2/Smad-3 signaling pathway (Bianco et al., 2010) (Figure 2).However, Cripto-1 can also regulate A/P axis specification independently of Nodal signaling (D'Andrea et al., 2008). In fact, Cripto-1F78A/F78A mouse embryos carrying the amino acid substitution F78A are unable to activate a Nodal signaling pathway but clearly establish an A/P axis and initiate germ layer formation and gastrulation movements (D'Andrea et al., 2008). During early mouse embryogenesis, Cripto-1 cannot be detected until prior to the gastrulation stage in the inner cell mass and in extra-embryonic trophoblast cells at day 4 of development. Increase in Cripto-1 expression is observed on day 6.5 of embryonic development when Cripto-1 is found in the primitive streak within epiblast cells undergoing EMT, which eventually give rise to mesoderm and endoderm (Bianco et al., 2010; de Castro et al., 2010). Cripto-1 is also detected in the ectoplacental cone at this stage. Cripto-1expression then decreases on day 7 when it is detected mostly in the truncus arterious of the developing heart.

Figure 2.

Cripto-1/Nodal dependent signaling pathway.

Cripto-1 is a co-receptor for Nodal, GDF-1 and GDF-3, allowing them to interact with ALK4 (ActRIB). The Cripto-1/Nodal/ALK4/ActRII receptor complex triggers activation and phosphorylation of Smad-2 and Smad-3. Phosphorylated Smad-2 and Smad-3 form a complex with Smad-4 and they translocate into the nucleus. In the nucleus, Smad-2/-3/-4 complex interacts with CREB binding protein (CBP)/p300 and activates transcription of specific target genes. The heat shock protein GRP78 can also enhance Cripto-1/Nodal-dependent signaling pathway, as discussed later in the text. GDF-1/-3: growth and differentiation factor-1/3, GRP78: glucose-regulated protein 78.

With the exception of the developing heart, little if any expression of Cripto-1 can be detected in the embryo after day 8 (Bianco et al., 2010; de Castro et al., 2010 as cited in Dono et al., 1993; Minchiotti et al., 2000). Disruption of Cripto-1 in Cripto-1 -/- embryos is embryonically lethal and results in the formation of embryos that possess a head without a trunk, demonstrating that there is a severe deficiency in embryonic mesoderm and endoderm without a loss of anterior neuroectoderm formation (de Castro et al., 2010 as cited in Ding et al. 1998). Initiation of the primitive heart tube in Cripto-1 -/- mice is severely inhibited due to failure in the development of functional beating cardiomyocytes, as demonstrated by the absence of expression of terminal myocardial differentiation genes (de Castro et al., 2010 as cited in Xu et al., 1998). Cripto-1 -/- embryonic bodies (EB) derived from Cripto-1-/-embryonic stem (ES) cells fail to form beating cardiomyocytes, while they differentiate into neuronal cells. Addition of a Cripto-1 recombinant protein to Cripto-1 -/-EBs during early time points (0–2 days) of differentiationis able to rescue cardiomyocyte differentiation. However, addition of Cripto-1 recombinant protein during later stages of differentiation fails to rescue cardiamyocyte differentiation, suggesting that Cripto-1 ability to promote cardiac differentiation of EB is restricted to an early window of this differentiation program (Minchiotti, 2005, as cited in Parisi et al., 2003).Interestingly, a microarray study revealed that Cripto-1 -/- ES cells had a reduced mRNA expression of the G protein coupled receptor APJ (also known as angiotensin type I-like receptor) and its ligand Apelin, as compared to control wild type ES cells. Gain of function experiments showed that APJ redirects the neural fate of Cripto-1 -/- ES cells and restores the cardiogenic program. Furthermore,comparison of Cripto-1,APJ and Apelinexpression profile in mouse embryo by in situ hybridization revealedthat expression of Apelin and APJ correlates with Cripto-1 expression. In fact, Apelin mRNA was clearly expressed in the developing primitive streak, whereas APJwas expressed in the primitive streak and adjacent mesoderm,resembling Cripto-1 expression pattern (D'Aniello et al., 2009). Therefore, APJ and Apelin are downstream targets of Cripto-1 signaling pathway and together with Cripto-1 they drive ES cells toward a cardiac lineage.

3.1. Cripto-1 in embryonic stem cells

Stem cells have the capacity to divide for an undetermined period of time and a potential to develop into many different cell types throughout early life and growth. Stem cells are distinguished from other cell types by two important characteristics. First, they possess the capability to differentiate into mature cells of any particular tissue (pluripotency). Second, they can undergo through numerous cell cycle divisions while maintaining their undifferentiated state (self-renewal). ES cells can be isolated from a 3- to 5-day-old embryo, called blastocyst, and have the potential to give rise to all specialized tissues and organs of a mature organism. Adult stem cells are found in various adult tissues, and function as a reservoirfor cells that are lost during injuryor disease (Bendall et al., 2008). Mouse embryonic stem cells (mES) or human embryonic stem cells (hES) have been very useful in the field of stem cell research. Comparison of gene expression profiles across species has shown that mouse and human ES cells share common highly conserved signaling pathways that regulate self-renewaland pluripotency, including the Cripto-1/Nodal signaling pathway. For example,in addition to Cripto-1, genes such as Oct-4, Lefty, Nodal, Sox-2, Utf-1 (undifferentiated embryonic cell transcription factor-1) andTert (telomerase reverse transcriptase) are highly enriched in both mouse and human ES cells (Wei et al., 2005). Additionally, Cripto-1 has been identified as a pluripotency marker also in primate ES cells together with Oct-4, Nanog, Sox-2, Tert, LeftyA, and Rex-1 (Chang et al., 2010). In 2007 a comparative study of a large and diverse set of hES cell lines assessed the expression pattern of commonly used stem cell markers. All the hES cells analyzed exhibited similar expression profile for several stem cell markers, including the glycolipid stage specific embryonic antigens SSEA3 and SSEA4, the keratan sulfate antigens TRA-1-60, TRA-1-81, and the developmentally regulated genes including Nanog,Oct-4,Dnmt3b,Gabrb3, GDF-3 and Cripto-1(Adewumi et al., 2007; Bianco et al., 2010; de Castro et al., 2010). Finally, Cripto-1 has been reported as a direct target gene of stem cell transcription factors (Bianco et al., 2010; de Castro et al., 2010; Hough et al., 2009). For instance, using the ChIP paired-end ditags method, Loh and collaborators mapped the binding sites of the transcription factors Oct-4 and Nanog in the mouse ES cell genome. Cripto-1 promoter was found to include Oct-4 and Nanog binding sites, suggesting that key modulators of stem cell self-renewal and pluripotentiality directly regulate Cripto-1 expression in ES cells(Bianco et al., 2010; de Castro et al., 2010; Loh et al., 2006).

3.1.1. Cross-talk of Cripto-1 with stem cell signature pathways

Several signaling pathways regulate in a coordinate fashion early embryonic development and stem cell proliferation, maintenance and differentiation. Some of these signaling cascades have been shown to cross-talk with Cripto-1 signaling, suggesting a pivotal role played by Cripto-1 in stem cell self-renewal and maintenance. Among these signaling pathways are genes in the Wnt/-cateninsignaling pathway, TGF- family members, the Notch pathway, and hypoxia inducible factor-1 alpha (HIF-1) (Bianco et al., 2010; de Castro et al., 2010). A schematic diagram of the cross-talk of Cripto-1/Nodal signaling with other stem cell signature signaling pathways is shown in figure 3.

Figure 3.

Interplay of Cripto-1/Nodal signaling with other embryonic stem cell signaling pathways.

Cripto-1 signaling is a downstream target of Oct-4, Nanog, Wnt/β-catenin, Notch and Hypoxia/HIF-1α pathways. Cripto-1 also mediates signaling of TGF-β family members and enhances Notch signaling by facilitation of Notch receptor maturation. TGF-: transforming growth factor-,HIF-1: hypoxia inducible factor-1, GDF-1/-3: growth and differentiation factor-1/-3, BMP-4: bone morphogenetic protein-4, ES cells: embryonic stem cells, mES cells: mouse embryonic stem cells.

Activation of the canonical Wnt/-catenin pathway has been reported to sustain the undifferentiated state of ES cells by triggering transcription of genes that regulate ES cell pluripotency and self-renewal, such as Oct-4, Nanog, Sox-2 and Cripto-1. For instance, Cripto-1 has been identified as a direct target gene in the canonical Wnt/-catenin signaling pathway during embryonic development and in colon carcinoma cell lines and tissues (Morkel et al., 2003). Remarkably, in -catenin-/-or Wnt3 -/-mutant mouse embryos, Cripto-1 expressionwas found to be dramatically downregulated, suggesting that the Wnt/-catenin signaling pathway is a positive regulator of Cripto-1 expression during embryonic development(Bianco et al., 2010). In addition, in Xenopus, the Cripto-1 ortholog XCR1/FRL-1 functions as a co-receptor for Wnt11 and together with frizzled receptor 7 and Glypican-4 mediates stabilization and activation of -catenin (Bianco et al., 2010). Several studies have clearly implicated Wnt/-catenin signaling pathway in initiation and maintenance of carcinomas of the skin, intestine, liver, and brain(Bianco et al., 2010; de Castro et al., 2010). Hence, the interaction between the Wnt/-catenin and Cripto-1 signaling pathways might be significant also in cancer initiation and progression. Activation of TGF-/Activin/Nodal signaling has also been reported to be required for the maintenance of undifferentiated state in human ES cells (James et al., 2005; Vallier et al., 2009). Some TGF- family members, including Nodal, GDF-1 and GDF-3, require Cripto-1 for signaling and they are critical for ES cell maintenance and self-renewal(Bianco et al., 2010). Furthermore,Activin, TGF-β and bone morphogenetic protein (BMP)-4 can directly regulate Cripto-1 expression by binding to smad binding elements (SBE) within the Cripto-1 promoter in human embryonal carcinoma cells and in human colon cancer cells (Mancino et al., 2008). GDF-3 and Cripto-1 have also been identified as ES cell markers that are enriched in a population of ES cells which are uncommitted and have high self-renewal capacity (Hough et al., 2009). Finally, Activin/TGF- signaling activity is required for Nanog expression in epiblast cells, suggesting a key role played by TGF- family members in maintaining ES pluripotency and self-renewal (Shin et al., 2011;Wang et al., 2009).The Notch pathway is a key regulator of many developmental processes during fetal and adult differentiation. Studies have reported that inappropriate activation of Notch signaling cascade contributes to tumorigenesis (Wilson & Radtke, 2006; Wang et al., 2009).Interaction between Notch and Cripto-1/Nodal signaling pathways has also been described. Analysis of the transcriptional regulatory regions within the mouse Nodal promoter has identifiedthe presence of CBF1 binding elements, suggesting a direct regulation of Nodal expression by Notch signaling (Bianco et al., 2010; as cited in Raya et al., 2003; Krebs et al 2003). In this regard, mouse embryo double mutants for Notch1 and Notch2 exhibit multiple defects in L/R asymmetry, which is regulated by Nodal. Moreover, a new insight into Notch and Cripto-1/Nodal signaling pathways hasbeen reported. Watanabe and colleagues (2009) using a yeast two-hybridsystem screened a mouse embryo or human colon cDNA prey library forpotential Cripto-1 binding partners. Six candidate genes were isolated, including the mouse Notch3. By coimmunoprecipitation analysis Cripto-1 was found to directly bind to all four mammalian Notch receptors. Surprisingly, binding of Cripto-1to Notch1 occurred mainly inside the cells in the endoplasmic reticulum/Golgi complex, where Cripto-1 enhanced cleavage of the Notch1 extracellular domain through a furin-like convertase. Enhanced cleavage of Notch1 receptor by Cripto-1 potentiates Notch signaling as demonstrated by enhanced ligand-induced activation of Notch signaling in Chinese hamster ovary cells expressing a CBF1-dependent Notch reporter assay (Watanabe et al., 2009). Hypoxia is an important regulator of stem cell proliferation and differentiation (Yeung et al., 2011). In fact, tissue stem cells reside within niches that are naturally hypoxic and low oxygen levels prevent their differentiation toward specific fates. Moreover, HIF-2α can directly regulate Oct-4 expression in ES cells by binding to hypoxia-responsive elements (HREs) within the promoter of mouse Oct-4. HIF-1α interacts with Notch signaling by binding to Notch intracellular domain and enhancing transcription of Notch downstream target genes Hes-1 and Hey-2. HIF-1α, in addition to regulating Notch1 signaling, can also regulate Cripto-1 expression by binding to HREs within the promoter region of mouse and human Cripto-1 gene in mouse ES cells and in human embryonal carcinoma cells(Bianco et al., 2009). In addition, hypoxic conditions enhanced differentiation of mES cells into beating cardiomyocytes when compared with mES cells grown under normoxic conditions. However, expression of Cripto-1 in mES was critical, because hypoxia was unable to induce differentiation of mES cells into cardiomyocytes in the absence of Cripto-1 expression.


4. Cripto-1 in cancer

Similarities between embryonic development and cellular transformation during oncogenesis have led to the identification of common signaling pathways, suggesting that reactivation of developmental signaling pathways might drive cell transformation and tumor progression in adult tissues (Bianco et al., 2010). Cripto-1 is a typical example of an embryonic gene that is re-expressed in human tumors, promoting cellular proliferation, migration, and tumor angiogenesis (Figure 4).

Figure 4.

Expression of Cripto-1 during embryogenesis and tumorigenesis.

Cripto-1 is highly expressed in undifferentiated embryonic stem cells and germ cells. Cripto-1 is important for mesoendoderm differentiation of ES cells and its expression is lost upon differentiation of ES cells toward the three germ cell layers. In the adult, Cripto-1 is re-expressed by tumor cells. Green color: no Cripto-1 expression, red color: Cripto-1 expression. ICM: Inner cell mass, ES: embryonic stem cells.

4.1. Cripto-1 oncogenic activities in vitro and in vivo

The first evidence of Cripto-1 oncogenic activity derives from studies demonstrating that Cripto-1 overexpression can induce in vitro transformation of a variety of cells, including NIH-3T3 fibroblasts and NOG-8 or CID9 mouse mammary epithelial cells (Ciardiello et al., 1991; Ciccodicola et al., 1989; Niemeyer et al., 1998).Furthermore, Cripto-1 can enhance migration and invasionof a variety of normal mammary epithelial cells and human breast and cervical carcinoma cells, suggesting the involvement of Cripto-1 in tumor progression (Ebert et al., 2000; Normanno et al., 2004a; Wechselberger et al., 2001). Cripto-1 can also function as a potent angiogenic protein both in vitro and in vivo, enhancing the proliferation, migration and invasion of human umbilical vascular endothelial cells and stimulating their differentiation into vascular-like structures in matrigel. Likewise, overexpression of Cripto-1 promotes in vivo neovascularization of MCF-7 xenografts, supporting a role for Cripto-1 in modulating tumor angiogenesis (Bianco et al., 2005a). SinceHIF-1 can enhance Cripto-1 expression by directly binding to the Cripto-1 promoter, it is possible that the hypoxic microenvironment within the growing tumor might enhance Cripto-1 expression, which in turn induces new vessel formation to sustain tumor growth (Bianco et al., 2009). Cripto-1 has also been directly implicated in mouse mammary tumor development (Sun et al., 2005; Wechselberger et al., 2005), as demonstrated by transgenic mouse models overexpressing the human Cripto-1 transgene in mouse mammary glands under the control of the MMTV or whey acidic protein (WAP) promoter (Sun et al., 2005; Wechselberger et al., 2005). The majority of nulliparous MMTV-Cripto-1 transgenic mice exhibited enhanced ductal branching, intraductal hyperplasias and hyperplastic alveolar nodules, and about 30-40% of aged multiparous female mice developed multifocal hyperplasias and papillary adenocarcinomas (Wechselberger et al., 2005). Interestingly, under a 2 years observation period, approximately 20% of female nulliparous or multiparous MMTV-Cripto-1 transgenic mice developed uterine leiomyosarcomas as compared to control mice. High levels of Cripto-1 transgene, phosphorylated forms of c-Src, AKT, glycogen synthase kinase-3(GSK-3β) and dephosphorylated active--catenin were detected in the uterine tumors collected from MMTV-Cripto-1 transgenic mice (Strizzi et al., 2007), suggesting a role for Cripto-1 during uterine tumorigenesis either by activation of c-Src and Akt and/or via cross-talk with the canonical Wnt/-catenin signaling pathway.Unlike the MMTV promoter,theWAP promoter is maximally active during mid-pregnancy and lactation. Approximately 50% of old nulliparous WAP-Cripto-1 mice developed multifocal intraductal hyperplasias, and more than 50% of multiparous WAP-Cripto-1 female mice developed multifocal mammary tumors of mixed histological subtypes (Sun et al., 2005). Histological analysis of the WAP-Cripto-1 mammary tumors revealed the presence of tumors containing glandular, papillary and undifferentiated carcinoma, as well as myoepithelioma and adeno-squamous carcinoma. Mammary tumors with mixed histology have also been described in MMTV-Wnt-1 transgenic mice, which have alterations in the canonical Wnt/-catenin pathway. Interestingly, hyperactivation of a canonical Wnt/-catenin pathway was detected in WAP-Cripto-1 mammary tumors, suggesting that the canonical Wnt/-catenin pathway together with Cripto-1 might play an important role during mammary transformation in vivo(Miyoshi et al., 2002a; Miyoshi et al., 2002b; Sun et al., 2005). Finally, several studies have demonstrated that Cripto-1, in addition to function as an oncogene in vitro and in animal models, is overexpressed at the mRNA and protein level in a wide variety of human tumors, including colorectal, breast, gastric, pancreatic, ovarian, endometrium, nasopharynx and lung carcinomas, while very little or no expression is detected in normal adult tissues. Therefore, the selective expression of Cripto-1 in cancer cells suggests that it represents a promising target in cancer therapy. For an extensive review on Cripto-1 expression in human tumors see de Castro et al., 2010.

4.1.1. Intracellular signaling pathways activated by Cripto-1 during oncogenic transformation

While Cripto-1 functions mostly in a Nodal-dependent manner during embryogenesis, several studies have demonstrated that Cripto-1 induces cellular proliferation, motility, survival and EMT in a Nodal-independent fashion. Following binding to the GPI-linked heparan sulphate proteoglycan Glypican-1, Cripto-1 induces activation and phosphorylation of the cytoplasmic tyrosine kinase c-Src, which in turn activates mitogen-activated protein kinase (MAPK)/Phosphatydil inositol 3’ kinase (PI3K)/Akt signaling pathways (Figure 5) (Bianco et al., 2005b).

Figure 5.

Nodal-independent Cripto-1 signaling pathway.

Cripto-1 upon binding to Glypican-1 activates MAPK and Akt signaling pathways during tumor progression, enhancing cell proliferation and survival. MAPK and PI3K/Akt pathways can also inhibit GSK-3β leading to activation and stabilization of β-catenin. GRP78 can also enhance Cripto-1 activation of the MAPK/Akt signaling pathways. GRP78: glucose-regulated protein 78, MAPK: mitogen-activated protein kinase, PI3K: phosphatydil inositol 3’ kinase, GSK3 : glycogen synthase kinase 3, TCF/LEF: T-cell factor/lymphoid enhancer factor, RSK: Ribosomal s6 kinase, STAT: signal transducers and activators of transcription.

Activation of the MAPK and PI3K/Akt signaling pathways by Cripto-1 is independent of Nodal and ALK4, since Cripto-1 can enhance phosphorylation of MAPK and Akt in cells lacking ALK4 and/or Nodal expression (Bianco et al., 2002). Furthermore, the tyrosine kinase c-Src is required by Cripto-1 to induce in vitro transformation of mouse mammary epithelial cells, indicating that inappropriate activation of c-Src by Cripto-1 in a Nodal- and ALK4-independent manner might play a key role in Cripto-1 tumorigenic activity (Bianco et al., 2003). The interaction between Cripto-1 and Gypican-1 occurs within lipid raft microdomains, regions of the cell membrane that are enriched in GPI-linked proteins (Bianco et al., 2003). Cripto-1 mitogenic signaling is also dependent upon binding to GRP78, an endoplasmic reticulum (ER) heat shock chaperone protein that is expressed on the cell surface of tumor cells (Shani et al., 2008). Indeed, disruption of the Cripto-1/GRP78 complex at the cell membrane interferes with Cripto-1 oncogenic activity in vitro, preventing Cripto-1 activation of MAPK/Akt signaling pathway (Figure 5). Interestingly, unlike Glypican-1, GRP78 is also important for Nodal-dependent Cripto-1 signaling, enhancing activation of the Smad-2/Smad-3 signaling pathway (Kelber et al., 2009). Furthermore, GRP78 enhanced Cripto-1-dependent activation of the c-Src/MAPK/Akt signaling pathways, increased cellular proliferation and reduced cell adhesion, as evidenced by a decrease in E-cadherin expression in breast cancer cells (Kelber et al., 2009).


5. Cripto-1 and Cancer Stem Cells

Cancer stem cells (CSCs), also known as tumor initiating cells, share characteristics associated with embryonic stem cells, specifically the ability to give rise to all cell types within a particular tumor tissue. CSCs were first identified in the hematopoietic system and later they have also been reported in solid cancers, including cancers of the breast, lung, prostate, colon, brain, head and neck, and pancreas (Bianco et al., 2010; de Castro et al., 2010). CSCs represent a distinct population of cancer cells with innate chemo- and radio-resistance and therefore are responsible of tumor relapse (Bianco et al., 2010; de Castro et al., 2010 as cited in Huntly and Gilliland 2010). Moreover, CSCs are capable to self-renew and regenerate the original phenotype of the tumor when implanted into immunodeficient mice (Visvader & Lindeman, 2008). Similarities between embryonic development and cell transformation during oncogenesis have led to the identification of common contributing pathways, suggesting that reactivation of developmental signaling pathways might drive cell transformation and tumor progression in adult tissues (Bianco et al., 2010). Cripto-1 is a typical example of a common gene shared by embryonic cells and cancer cells contributing to early embryogenesis and cancer progression. More importantly, Cripto-1 is enriched in a subpopulation of cancer cells with stem-like characteristics. For instance, Watanabe and collaborators (2010) described a heterogeneous Cripto-1 expression pattern in human embryonal carcinoma (EC) with segregation of these cells into two distinct populations portraying high and low Cripto-1 expression. EC cells are pluripotent stem cells derived from germ cell teratocarcinomas and they represent the malignant counterparts of human ES cells. Interestingly, these two subpopulations showed different gene expression profiles and different in vitroand in vivo tumorigenic capability. The Cripto-1 high subpopulation of EC cells formed tumor spheres in a serum-free suspension culture with an efficiency significantly higher than the Cripto-1 low expressing EC cells. Furthermore, the Cripto-1 high expressing EC cells were able to generate tumors larger in size and with a shorter tumor latency period compared with tumors derived from Cripto-1 low expressing EC cells when injected subcutaneously into nude mice. Finally, regulators of pluripotent ES cells, such as Activin/Nodal signaling and the transcription factors Nanog and Oct-4,positively regulated Cripto-1 expression in Cripto-1 high expressing EC cells, suggesting the existence of a core transcriptional regulatory network of pluripotent stem cell transcription factors that cross-regulate each other expression(Loh et al., 2006). However, Cripto-1 expression is dispensable for pluripotent stem cell gene expression in EC cells, since siRNA-mediatedknockdownof Cripto-1 has no effect on the expression of ES-related genes including Oct-4, Nanog, Sox-2 and Lefty. In another study, Cripto-1 has been exploited as a potential melanoma stem cells candidate marker in human malignant melanomas (Strizzi et al., 2008). Strizzi and colleagues,by FACS cell sorting based on Cripto-1 expression, isolated from a human melanoma cell line a subpopulation with stem-like characteristics. The Cripto-1 positive subpopulation of melanoma cells represented a relatively smaller size population with a more spindle-shaped morphology, and showed increased expression of the stem cell associated transcription factors, Oct-4 and Nanog, as compared to the parental melanoma cells. Finally, Cripto-1 and the stem cell markers Oct-4 and SUZ-12 were identified in a small subpopulation of stem-like cells in hormone-responsive and nonresponsive prostate tumor cell (Cocciadiferro et al., 2009). Altogether, these findings suggest that Cripto-1 might be useful in the identification of a subpopulation of cancer cells with stem like behavior that are resistant to conventional therapy and are therefore a major obstacle in the clinical treatment of cancer patients.

5.1. Cancer stem cells and EMT

During embryogenesis, tumor progression and metastasis, epithelial cells undergo dramatic morphological changes, acquiring mesenchymal properties in a process known as EMT. In the embryo, Cripto-1 is detected at high levels in epiblast cells undergoing EMT, which migrate through the primitive streak, eventually giving rise to the mesoderm and endoderm (Bianco et al., 2005b; Strizzi et al., 2005).In the tumor, the expression of EMT regulators at the tumor periphery is critical for tumor cells to acquire a mesenchymal phenotype that allow them to locally invade and escape from the primary tumor site, leading to the establishment of metastatic lesions(Micalizzi et al., 2010a). Cripto-1 is involved in tumor epithelial cells plasticity and may be an important EMT regulator together with Snail, Slug, Twist, and Six1 (Micalizzi et al., 2010b). It has been shown that mammary gland hyperplasias and tumors derived from MMTV-Cripto-1 transgenic mice express molecular markers and signaling molecules characteristics of EMT, suggesting that Cripto-1 might play an important role in facilitating migration and invasion of tumor cells (Strizzi et al., 2004). These findings might be significant since emerging evidence has suggested a link between stem cellsand EMT (Hollier et al., 2009). In fact, EMT induction in immortalized human mammary epithelial cells resulted in the expression of stem cell markers and increased ability to form mammospheres in vitro, suggesting an important role for EMT in generating cancer stem-like cells in human breast tumors (Mani et al., 2008). Since Cripto-1 has been found to promote EMT in mouse mammary epithelial cells and mouse mammary tumors, contributing to a more aggressive mesenchymal phenotype, it is possible that Cripto-1 might support self-renewal, invasiveness and metastatic abilities of breast cancer stem-like cells through induction of an EMT program (Strizzi et al., 2004).


6. Cripto-1 as target for cancer therapy

High expression of Cripto-1 in human carcinomas and its enrichment in a stem-like cancer cell subpopulation strongly support Cripto-1 as a promising candidate for therapeutic intervention in cancer. Two different therapeutic approaches have been successfully used to impair Cripto-1 activity in cancer cells, including anti-Cripto-1 antisense (AS) oligonucleotides and neutralizing monoclonal antibodies (Adkins et al., 2003; Hu et al., 2007; Normanno et al., 1996; Normanno et al., 2004b). For instance, a significant growth inhibition in vitro has been observed in ovarian, breast and colon cancer cells treated with anti-Cripto-1 AS oligonucleotides. A synergistic growth inhibitory effect was detected when anti-Cripto-1 AS oligonucleotides were combined together with oligonucleotides against TGF-α and amphiregulin (AREG), indicating that a variety of growth factors might cooperate in stimulating cancer cell proliferation (Casamassimi et al., 2000; De Luca et al., 2000; De Luca et al., 1999; Normanno et al., 2004b). Additionally, combination of anti-Cripto-1 AS oligonucleotides with anti-TGF-α and anti-AREG AS oligonucleotides was more effective in vivoas compared to single AS oligonucleotide administration, inhibiting the growth of colon cancer tumor xenografts in nude mice in a dose dependent manner (De Luca et al. 2000). Neutralizing antibodies that bind Cripto-1 have also been generated(Adkins et al., 2003; Hu & Xing, 2005). In particular, Adkins and colleagues of Biogen-Idec have generated a panel of monoclonal antibodies (mAbs) directed against a human recombinant Cripto-1 protein expressed as a human IgG1 Fc fusion protein (Adkins et al. 2003). The mAbs are capable to recognize different domains of the Cripto-1 protein, detecting its expression in human breast and colon tumor tissue samples and in human cancer cell lines. Among these anti-Cripto-1 mAbs, anti-CFC mAbs showed blocking activities in vitro and in vivoby interfering with the binding of Cripto-1 with ALK4 through the CFC domain. The anti-CFC blocking antibodies also blocked the interaction of Cripto-1 with Activin B (Adkins et al. 2003), restoring the growth inhibitory function of Activin B in tumor cells. Recently, among these anti-Cripto-1 mAbs, an N-terminal anti-Cripto-1 antibody has been selected to target Cripto-1 in human tumors, due to the higher binding affinity and range of reactivity of this antibody with tumor-derived Cripto-1 (Kelly et al., 2011). A humanized form of the anti-Cripto-1 N-terminal monoclonal antibody-conjugated to a DM4 toxin is currently been evaluated in phase I clinical trials for treatment of patients with refractory or relapsed Cripto-1 positive solid tumors (A phase I study of BIIB015 in relapsed/refractory solid tumors, protocol ID 207ST101/NCT00674947) (Bianco & Salomon, 2010). BIIB015 showed specificity for Cripto-1 in vitro and in vivo with a clinical response ranging between 50% of tumor inhibition to complete tumor regression in xenograft mouse models inoculated with lung (Calu-6), colon (CT-3), testicular (NCCIT) or breast (MDA-MB-231) human tumor cell lines (Kelly et al., 2011).In addition to mouse monoclonal antibodies against Cripto-1, anti-Cripto-1 rat monoclonal antibodies have also been generated. Rat anti-Cripto-1 monoclonal antibodies inhibited tumor cell growth and increased sensitivity of LS174T human colon cancer cells and MCF-7 human breast cancer cells to the cytotoxic effects of chemotherapeutic agents such as cisplatin, 5-Fluorouracil, carboplatin and epirubicin (Xing et al., 2004). Furthermore, a C13 rat monoclonal antibody inhibited cancer cell growth in vivo in LS174T tumor xenografts in SCID mice, inducing up to 80% growth inhibition of established tumors as compared to an untreated control groups. Interestingly, C4 and C13 rat monoclonal antibodies were also highly effective in reducing tumor growth of a human leukemia multidrug resistant (MDR) cell line (CEM/A7R) both in vitro and in vivo in an established xenograft tumor model (Hu et al., 2007).

6.1. Cripto-1 as a target for therapy in neurodegenerative and muscle degenerative diseases

Recent findings have demonstrated that Cripto-1 is a key player in the signaling pathway controlling neural induction in ES cells. Parisi and collaborators showed that Cripto-1 negatively regulated neuronal differentiation of ES cells (Parisi et al., 2003). Furthermore, disruption of Cripto-1 expression in mouse ES cells enhances neurogenesis and midbrain dopaminergic differentiation in vitro(Parish et al., 2005; Sonntag et al., 2005). These results suggest that blocking Cripto-1 expression and activity may provide a novel insight into the treatment of neurodegenerative diseases. Parkinson’s disease is a progressive neurodegenerative disorder characterized by degeneration of dopaminergic neurons of the substantia nigra. Therefore methods that channel undifferentiated ES cells into dopaminergic neurons are under extensive evaluation, aiming to improve the safety of ES cells grafting that often results in uncontrolled proliferation and teratoma formation (Parish & Arenas, 2007). In a rat animal model of Parkinson’s disease, mouse ES cells that are null for Cripto-1 expression (Cripto-1-/- ES cells), when grafted at low density into rats, differentiated into neuronal cells in the brain and were able to restore normal behavior without producing teratomas (Parish et al., 2005). Recently, a tetrameric tripeptide, which prevents Cripto-1/ALK4 interaction and interferes with Cripto-1 signaling was identified(Lonardo et al., 2010). The Cripto-1 blocking peptide was able to induce formation of neuroectoderm and increased midbrain dopaminergic neuron differentiation of mouse ES cells in vitro and in vivo(Lonardo et al., 2010). Moreover, mouse ES cells treated with Cripto-1 blocking peptide enhanced functional recovery and reduced tumor formation in Parkinsonian rats (Lonardo et al., 2010). Overexpression of Cripto-1 has also been observed in the cerebral cortical tissues of macaques that had been infected with a chimeric simian human immunodeficiency virus (SHIV) by cDNA array analysis (Stephens et al., 2006). SHIV enters the central nervous system (CNS) early after inoculation and cause encephalitis, characterized by transient meningitis and astrocytosis. Immunohistochemical analysis and RT-PCR confirmed widespread expression of Cripto-1 in the brains of SHIV-infected macaques. Although the functions of Cripto-1 in the neurons of the adult brain and the overexpression in the brains of SHIV-infected macaques are unclear, Cripto-1 may play a neuroinflammatory role and targeting Cripto-1 with various approaches, such as the tetrameric tripeptide described by Lonardo and colleagues, might inhibit progression of neurodegenerative disease in mammals. Cripto-1 may also be involved in degenerative muscle diseases, such as muscular dystrophy and spinal muscular atrophy. These diseases are characterized by skeletal muscle loss and few therapeutic approaches are available to restore the function of the lost muscle tissue (Tedesco et al., 2010). Cripto-1 is highly expressed in myoblast cells of regenerative muscles, whereas no expression of Cripto-1 is detected in normal muscle fibers. Furthermore, Cripto-1 induced a dose-dependent increase in proliferation and migration of myogenic precursor cells in vitro and enhanced skeletal muscle regeneration and angiogenesis after injury in vivo(Bianco & Salomon, 2010). These studies clearly suggest an involvement of Cripto-1 in neurodegenerative and muscle degenerative disease. Therefore, approaches that have been developed to target Cripto-1 in cancer might benefit also different diseases.


7. Conclusions

Critical signaling pathways are involved in modulating embryonic stem cell fate and behavior, maintaining a delicate balance between survival and self-renewal signals. Among these ES cell “signature” pathways, Cripto-1 is a critical gene that is used by ES cells. For instance, Cripto-1 is either a downstream target of ES transcription factors and/or signaling pathways or can modulate other ES cell signaling cascades (Fig. 3). Further, deregulation of stem cell self-renewal is probably a requirement for the initiation and formation of CSCsand therefore embryonic stem cell signature genes are also involved in cancer formation. Cripto-1 is indeed an embryonic gene that is re-expressed in an aberrant spatial and temporal manner in a variety of human tumors. Recent evidence has clearly demonstrated that Cripto-1 is expressed by a subset of cancer cells with stem-like characteristics (Watanabe et al., 2010). CSCs are considered to be a major obstacle in the complete eradication of tumors due their innate resistance to conventional therapy and therefore identification of surface markers that might discriminateCSCs from the bulk population of tumor cells is under active investigation. Therefore, Cripto-1 targeting in human tumors might have a major breakthrough in cancer therapy. Several approaches have been used to target Cripto-1 in cancer cells in vitro and in vivo, from antisense oligonucleotides to blocking monoclonal antibodies (Bianco & Salomon, 2010). Translation of Cripto-1 research to a clinical setting has been recently achieved. In fact, a humanized anti-Cripto-1 antibody conjugated with a potent cytotoxin is currently being evaluated in a Phase I clinical study in cancer patients. In conclusion, a complete understanding of Cripto-1 signaling in stem cell biology offers a great promise for improving stem cell mediated regenerative therapy as wellas cancer therapy.


  1. 1. Adewumi, O., Aflatoonian, B., Ahrlund-Richter, L., Amit, M., Andrews, P.W., Beighton, G., Bello, P.A., Benvenisty, N., Berry, L.S., Bevan, S., Blum, B., Brooking, J., Chen, K.G., Choo, A.B., Churchill, G.A., Corbel, M., Damjanov, I., Draper, J.S., Dvorak, P., Emanuelsson, K., Fleck, R.A., Ford, A., Gertow, K., Gertsenstein, M., Gokhale, P.J., Hamilton, R.S., Hampl, A., Healy, L.E., Hovatta, O., Hyllner, J., Imreh, M.P., Itskovitz-Eldor, J., Jackson, J., Johnson, J.L., Jones, M., Kee, K., King, B.L., Knowles, B.B., Lako, M., Lebrin, F., Mallon, B.S., Manning, D., Mayshar, Y., McKay, R.D., Michalska, A.E., Mikkola, M., Mileikovsky, M., Minger, S.L., Moore, H.D., Mummery, C.L., Nagy, A., Nakatsuji, N., O’Brien, C.M., Oh, S.K., Olsson, C., Otonkoski, T., Park, K.Y., Passier, R., Patel, H., Patel, M., Pedersen, R., Pera, M.F., Piekarczyk, M.S., Pera, R.A., Reubinoff, B.E., Robins, A.J., Rossant, J., Rugg-Gunn, P., Schulz, T.C., Semb, H., Sherrer, E.S., Siemen, H., Stacey, G.N., Stojkovic, M., Suemori, H., Szatkiewicz, J., Turetsky, T., Tuuri, T., van den Brink, S., Vintersten, K., Vuoristo, S., Ward, D., Weaver, T.A., Young, L.A. & Zhang, W. 2007. Characterization of human embryonic stem cell lines by the International Stem Cell Initiative. Nat Biotechnol, Vol. 25,No.7, (Jul and 2007), pp. (803-816), 1087-0156 (Print)
  2. 2. AdkinsH. B.BiancoC.SchifferS. G.RayhornP.ZafariM.CheungA. E.OrozcoO.OlsonD.De LucaA.ChenL. L.MiatkowskiK.BenjaminC.NormannoN.WilliamsK. P.JarpeM.Le PageD.SalomonD.SanicolaM.2003Antibody blockade of the Cripto CFC domain suppresses tumor cell growth in vivoJ Clin Invest, 4Aug and 2003), 575587
  3. 3. BendallS. C.StewartM. H.BhatiaM.2008Human embryonic stem cells: lessons from stem cell niches in vivoRegen Med, 3May and 2008), 365376X (Electronic)
  4. 4. BiancoC.AdkinsH. B.WechselbergerC.SenoM.NormannoN.De LucaA.SunY.KhanN.KenneyN.EbertA.WilliamsK. P.SanicolaM.SalomonD. S.2002Cripto-1 activates nodal- and ALK4-dependent and-independent signaling pathways in mammary epithelial Cells. Mol Cell Biol, 8Apr and 2002), 25862597
  5. 5. BiancoC.CottenC.LonardoE.StrizziL.BaratyC.MancinoM.GonzalesM.WatanabeK.NagaokaT.BerryC.AraiA. E.MinchiottiG.SalomonD. S.2009Cripto-1 is required for hypoxia to induce cardiac differentiation of mouse embryonic stem cellsAm J Pathol, 5Nov and 2009), 21462158
  6. 6. BiancoC.MysliwiecM.WatanabeK.MancinoM.NagaokaT.GonzalesM.SalomonD. S.2008Activation of a Nodal-independent signaling pathway by Cripto-1 mutants with impaired activation of a Nodal-dependent signaling pathwayFEBS Lett, 29Dec 10 and 2008), 39974002Print)
  7. 7. BiancoC.RangelM. C.CastroN. P.NagaokaT.RollmanK.GonzalesM.SalomonD. S.Roleof.Criptoinstem.cellmaintenance.malignantprogression.Am J Pathol, 2Aug and 532540
  8. 8. BiancoC.RangelM. C.CastroN. P.NagaokaT.RollmanK.GonzalesM.SalomonD. S.2010Role of Cripto-1 in stem cell maintenance and malignant progressionAm J Pathol, 2Aug and 2010), 532540Electronic)
  9. 9. BiancoC.SalomonD. S.2010Targeting the embryonic gene Cripto-1 in cancer and beyondExpert Opin Ther Pat, 12Dec and 2010), 17391749Electronic)
  10. 10. BiancoC.StrizziL.EbertA.ChangC.RehmanA.NormannoN.GuedezL.SalloumR.GinsburgE.SunY.KhanN.HirotaM.Wallace-JonesB.WechselbergerC.VonderhaarB. K.TosatoG.Stetler-StevensonW. G.SanicolaM.SalomonD. S.2005aRole of human cripto-1 in tumor angiogenesisJ Natl Cancer Inst, 2Jan 19 and 2005a), 132141
  11. 11. BiancoC.StrizziL.NormannoN.KhanN.SalomonD. S.2005bCripto-1: an oncofetal gene with many faces.Curr Top Dev Biol, 67and 2005b), 85133
  12. 12. BiancoC.StrizziL.RehmanA.NormannoN.WechselbergerC.SunY.KhanN.HirotaM.AdkinsH.WilliamsK.MargolisR. U.SanicolaM.SalomonD. S.2003A Nodal- and ALK4-independent signaling pathway activated by Cripto-1 through Glypican-1 and c-Src.Cancer Res, 6Mar 15 and 2003), 11921197
  13. 13. CasamassimiA.De LucaA.AgrawalS.StrombergK.SalomonD. S.NormannoN.2000EGF-related antisense oligonucleotides inhibit the proliferation of human ovarian carcinoma cells.Ann Oncol, 3Mar and 2000), 319325Print)
  14. 14. ChangT. C.LiuY. G.EddyC. A.JacobyE. S.BinkleyP. A.BrzyskiR. G.SchenkenR. S.2010Derivation and Characterization of Novel Nonhuman Primate Embryonic Stem Cell Lines from In Vitro-Fertilized Baboon Preimplantation EmbryosStem Cells Dev, Vol. (Nov 4 and 2010), 15578534Electronic)
  15. 15. CiardielloF.DonoR.KimN.PersicoM. G.SalomonD. S.1991Expression of cripto, a novel gene of the epidermal growth factor gene family, leads to in vitro transformation of a normal mouse mammary epithelial cell line. Cancer Res, 3Feb 1 and 1991), 10511054
  16. 16. CiccodicolaA.DonoR.ObiciS.SimeoneA.ZolloM.PersicoM. G.1989Molecular characterization of a gene of the ‘EGF family’ expressed in undifferentiated human NTERA2 teratocarcinoma cells.Embo J, 7Jul and 1989), 19871991
  17. 17. CocciadiferroL.MiceliV.KangK. S.PolitoL. M.TroskoJ. E.CarrubaG.2009Profiling cancer stem cells in androgen-responsive and refractory human prostate tumor cell lines. Ann N Y Acad Sci, 1155Feb and 2009), 257262
  18. 18. D’AndreaD.LiguoriG. L.Le GoodJ. A.LonardoE.AnderssonO.ConstamD. B.PersicoM. G.MinchiottiG.2008Cripto promotes A-P axis specification independently of its stimulatory effect on Nodal autoinductionJ Cell Biol, 3Feb 11 and 2008), 597605Electronic)
  19. 19. D’AnielloC.LonardoE.IaconisS.GuardiolaO.LiguoroA. M.LiguoriG. L.AutieroM.CarmelietP.MinchiottiG.2009G protein-coupled receptor APJ and its ligand apelin act downstream of Cripto to specify embryonic stem cells toward the cardiac lineage through extracellular signal-regulated kinase/p70S6 kinase signaling pathwayCirc Res, 3Jul 31 and 2009), 231238Electronic)
  20. 20. de CastroN. P.RangelM. C.NagaokaT.SalomonD. S.BiancoC.2010Cripto-1: an embryonic gene that promotes tumorigenesisFuture Oncol, 7Jul and 2010), 11271142Electronic)
  21. 21. De LucaA.ArraC.D’AntonioA.CasamassimiA.LositoS.FerraroP.CiardielloF.SalomonD. S.NormannoN.2000Simultaneous blockage of different EGF-like growth factors results in efficient growth inhibition of human colon carcinoma xenografts.Oncogene51Nov 30 and 2000), 58635871Print)
  22. 22. De LucaA.CasamassimiA.SelvamM. P.LositoS.CiardielloF.AgrawalS.SalomonD. S.NormannoN.1999EGF-related peptides are involved in the proliferation and survival of MDA-MB-468 human breast carcinoma cells.Int J Cancer, 4Feb 9 and 1999), 589594
  23. 23. EbertA. D.WechselbergerC.NeesM.ClairT.SchallerG.Martinez-LacaciI.Wallace-JonesB.BiancoC.WeitzelH. K.SalomonD. S.2000Cripto-1-induced increase in vimentin expression is associated with enhanced migration of human Caski cervical carcinoma cellsExp Cell Res, 1May 25 and 2000), 223229
  24. 24. HollierB. G.EvansK.ManiS. A.2009The epithelial-to-mesenchymal transition and cancer stem cells: a coalition against cancer therapiesJ Mammary Gland Biol Neoplasia, 1Mar and 2009), 2943
  25. 25. HoughS. R.LaslettA. L.GrimmondS. B.KolleG.PeraM. F.2009A continuum of cell states spans pluripotency and lineage commitment in human embryonic stem cellsPLoS One, 11and 2009), e7708
  26. 26. HuX. F.LiJ.YangE.VandervalkS.XingP. X.2007Anti-Cripto Mab inhibit tumour growth and overcome MDR in a human leukaemia MDR cell line by inhibition of Akt and activation of JNK/SAPK and bad death pathways.Br J Cancer, 6Mar 26 and 2007), 918927
  27. 27. HuX. F.XingP. X.2005Cripto monoclonal antibodies.Drug News Perspect, 5Jun and 2005), 293303Print)
  28. 28. JamesD.LevineA. J.BesserD.Hemmati-BrivanlouA.2005TGFbeta/activin/nodal signaling is necessary for the maintenance of pluripotency in human embryonic stem cells.Development, 6Mar and 2005), 12731282Print)
  29. 29. KelberJ. A.PanopoulosA. D.ShaniG.BookerE. C.BelmonteJ. C.ValeW. W.GrayP. C.2009Blockade of Cripto binding to cell surface GRP78 inhibits oncogenic Cripto signaling via MAPK/PI3K and Smad2/3 pathwaysOncogene24Jun 18 and 2009), 23242336Electronic)
  30. 30. KellyR. K.OlsonD. L.SunY.WenD.WorthamK. A.AntognettiG.CheungA. E.OrozcoO. E.YangL.BaillyV.SanicolaM.2011An antibody-cytotoxic conjugate, BIIB015, is a new targeted therapy for Cripto positive tumoursEur J Cancer, Vol. (Mar 31 and 2011), 18790852Electronic)
  31. 31. LohY. H.WuQ.ChewJ. L.VegaV. B.ZhangW.ChenX.BourqueG.GeorgeJ.LeongB.LiuJ.WongK. Y.SungK. W.LeeC. W.ZhaoX. D.ChiuK. P.LipovichL.KuznetsovV. A.RobsonP.StantonL. W.WeiC. L.RuanY.LimB.NgH. H.2006The Oct4 and Nanog transcription network regulates pluripotency in mouse embryonic stem cells.Nat Genet, 4Apr and 2006), 431440Print)
  32. 32. LonardoE.ParishC. L.PonticelliS.MarascoD.RibeiroD.RuvoM.De FalcoS.ArenasE.MinchiottiG.2010A small synthetic cripto blocking Peptide improves neural induction, dopaminergic differentiation, and functional integration of mouse embryonic stem cells in a rat model of Parkinson’s diseaseStem Cells8Aug and 2010), 13261337Electronic)
  33. 33. MancinoM.StrizziL.WechselbergerC.WatanabeK.GonzalesM.HamadaS.NormannoN.SalomonD. S.BiancoC.2008Regulation of human Cripto-1 gene expression by TGF-beta1 and BMP-4 in embryonal and colon cancer cells.J Cell Physiol, 1Apr and 2008), 192203Electronic)
  34. 34. ManiS. A.GuoW.LiaoM. J.EatonE. N.AyyananA.ZhouA. Y.BrooksM.ReinhardF.ZhangC. C.ShipitsinM.CampbellL. L.PolyakK.BriskenC.YangJ.WeinbergR. A.2008The epithelial-mesenchymal transition generates cells with properties of stem CellsCell, 4May 16 and 2008), 704715
  35. 35. MicalizziD. S.FarabaughS. M.FordH. L.2010aEpithelial-mesenchymal transition in cancer: parallels between normal development and tumor progressionJ Mammary Gland Biol Neoplasia, 2Jun and 2010a), 117134Electronic)
  36. 36. MicalizziD. S.WangC. A.FarabaughS. M.SchiemannW. P.FordH. L.2010bHomeoprotein Six1 increases TGF-beta type I receptor and converts TGF-beta signaling from suppressive to supportive for tumor growth.Cancer Res, 24Dec 15 and 2010b), 1037110380Electronic)
  37. 37. MinchiottiG.2005Nodal-dependant Cripto signaling in ES cells: from stem cells to tumor biology.Oncogene37Aug 29 and 2005), 56685675Print)
  38. 38. MinchiottiG.MancoG.ParisiS.LagoC. T.RosaF.PersicoM. G.2001Structure-function analysis of the EGF-CFC family member Cripto identifies residues essential for nodal signalling.Development, 22Nov and 2001), 45014510Print)
  39. 39. MinchiottiG.ParisiS.LiguoriG.SignoreM.LaniaG.AdamsonE. D.LagoC. T.PersicoM. G.2000Membrane-anchorage of Cripto protein by glycosylphosphatidylinositol and its distribution during early mouse development.Mech Dev, 2Feb and 2000), 133142Print)
  40. 40. MiyoshiK.RosnerA.NozawaM.ByrdC.MorganF.Landesman-BollagE.XuX.SeldinD. C.SchmidtE. V.TaketoM. M.RobinsonG. W.CardiffR. D.HennighausenL.2002aActivation of different Wnt/beta-catenin signaling components in mammary epithelium induces transdifferentiation and the formation of pilar tumors.Oncogene36Aug 15 and 2002a), 55485556Print)
  41. 41. MiyoshiK.ShillingfordJ. M.Le ProvostF.GounariF.BronsonR.vonBoehmer. H.TaketoM. M.CardiffR. D.HennighausenL.KhazaieK.2002bActivation of beta-catenin signaling in differentiated mammary secretory cells induces transdifferentiation into epidermis and squamous metaplasias. Proc Natl Acad Sci U S A, 1Jan 8 and 2002b), 219224Print)
  42. 42. MorkelM.HuelskenJ.WakamiyaM.DingJ.van de WeteringM.CleversH.TaketoM. M.BehringerR. R.ShenM. M.BirchmeierW.2003Beta-catenin regulates Cripto- and Wnt3-dependent gene expression programs in mouse axis and mesoderm formation.Development, 25Dec and 2003), 62836294
  43. 43. NiemeyerC. C.PersicoM. G.AdamsonE. D.1998Cripto: roles in mammary cell growth, survival, differentiation and transformation.Cell Death Differ, 5May and 1998), 440449
  44. 44. AngelisE.SelvamM. P.GrassiM.MagliuloG.TortoraG.BiancoA. R.MendelsohnJ.SalomonD. S.CiardielloF.1996Growth inhibition of human colon carcinoma cells by combinations of anti-epidermal growth factor-related growth factor antisense oligonucleotides.Clin Cancer Res, 3Mar and 1996), 601609Print)
  45. 45. NormannoN.De LucaA.BiancoC.MaielloM. R.CarrieroM. V.RehmanA.WechselbergerC.ArraC.StrizziL.SanicolaM.SalomonD. S.2004aCripto-1 overexpression leads to enhanced invasiveness and resistance to anoikis in human MCF-7 breast cancer cells.J Cell Physiol, 1Jan and 2004a), 3139
  46. 46. NormannoN.De LucaA.MaielloM. R.BiancoC.MancinoM.StrizziL.ArraC.CiardielloF.AgrawalS.SalomonD. S.2004bCRIPTO-1: a novel target for therapeutic intervention in human carcinoma.Int J Oncol, 4Oct and 2004b), 10131020
  47. 47. ParishC. L.ArenasE.2007Stem-cell-based strategies for the treatment of Parkinson’s diseaseNeurodegener Dis, 4and 2007), 339347Print)
  48. 48. ParishC. L.ParisiS.PersicoM. G.ArenasE.MinchiottiG.2005Cripto as a target for improving embryonic stem cell-based therapy in Parkinson’s disease.Stem Cells, 4Apr and 2005), 471476Print)
  49. 49. ParisiS.D’AndreaD.LagoC. T.AdamsonE. D.PersicoM. G.MinchiottiG.2003Nodal-dependent Cripto signaling promotes cardiomyogenesis and redirects the neural fate of embryonic stem cellsJ Cell Biol, 2Oct 27 and 2003), 303314Print)
  50. 50. SchifferS. G.FoleyS.KaffashanA.HronowskiX.ZichittellaA. E.YeoC. Y.MiatkowskiK.AdkinsH. B.DamonB.WhitmanM.SalomonD.SanicolaM.WilliamsK. P.2001Fucosylation of Cripto is required for its ability to facilitate nodal signaling.J Biol Chem, 41Oct 12 and 2001), 3776937778Print)
  51. 51. ShaniG.FischerW. H.JusticeN. J.KelberJ. A.ValeW.GrayP. C.2008GRP78 and Cripto form a complex at the cell surface and collaborate to inhibit transforming growth factor beta signaling and enhance cell growth. Mol Cell Biol, 2Jan and 2008), 666677Electronic) 0270-7306 (Linking)
  52. 52. ShiS.GeC.LuoY.HouX.HaltiwangerR. S.StanleyP.2007The threonine that carries fucose, but not fucose, is required for Cripto to facilitate Nodal signaling.J Biol Chem, 28Jul 13 and 2007), 2013320141Print)
  53. 53. ShinM.AlevC.WuY.NagaiH.ShengG.2011Activin/TGF-beta signaling regulates Nanog expression in the epiblast during gastrulationMech Dev, Vol. (Mar 22 and 2011), 18726356Electronic)
  54. 54. SonntagK. C.SimantovR.BjorklundL.CooperO.PruszakJ.KowalkeF.GilmartinJ.DingJ.HuY. P.ShenM. M.IsacsonO.2005Context-dependent neuronal differentiation and germ layer induction of Smad4-/- and Cripto-/- embryonic stem cells.Mol Cell Neurosci, 3Mar and 2005), 417429Print)
  55. 55. StephensE. B.JacksonM.CuiL.PacyniakE.ChoudhuriR.LivermanC. S.SalomonD. S.BermanN. E.2006Early dysregulation of cripto-1 and immunomodulatory genes in the cerebral cortex in a macaque model of neuroAIDSNeurosci Lett, 2Dec 20 and 2006), 9499Print)
  56. 56. StrizziL.AbbottD. E.SalomonD. S.HendrixM. J.2008Potential for cripto-1 in defining stem cell-like characteristics in human malignant melanomaCell Cycle13Jul 1 and 2008), 19311935
  57. 57. StrizziL.BiancoC.HirotaM.WatanabeK.MancinoM.HamadaS.RaafatA.LawsonS.EbertA.D’AntonioA.LositoS.NormannoN.SalomonD.2007Development of leiomyosarcoma of the uterus in MMTV-CR-1 transgenic mice.J Pathol, 1Jan and 2007), 3644
  58. 58. StrizziL.BiancoC.NormannoN.SalomonD.2005Cripto-1: a multifunctional modulator during embryogenesis and oncogenesis.Oncogene37Aug 29 and 2005), 57315741
  59. 59. StrizziL.BiancoC.NormannoN.SenoM.WechselbergerC.Wallace-JonesB.KhanN. I.HirotaM.SunY.SanicolaM.SalomonD. S.2004Epithelial mesenchymal transition is a characteristic of hyperplasias and tumors in mammary gland from MMTV-Cripto-1 transgenic mice.J Cell Physiol, 2Nov and 2004), 266276
  60. 60. SunY.StrizziL.RaafatA.HirotaM.BiancoC.FeigenbaumL.KenneyN.WechselbergerC.CallahanR.SalomonD. S.2005Overexpression of human Cripto-1 in transgenic mice delays mammary gland development and differentiation and induces mammary tumorigenesis.Am J Pathol, 2Aug and 2005), 585597
  61. 61. TedescoF. S.DellavalleA.Diaz-ManeraJ.MessinaG.CossuG.2010Repairing skeletal muscle: regenerative potential of skeletal muscle stem cellsJ Clin Invest, 1Jan 4 and 2010), 1119Electronic)
  62. 62. VallierL.MendjanS.BrownS.ChngZ.TeoA.SmithersL. E.TrotterM. W.ChoC. H.MartinezA.Rugg-GunnP.BronsG.PedersenR. A.2009Activin/Nodal signalling maintains pluripotency by controlling Nanog expressionDevelopment8Apr and 2009), 13391349
  63. 63. VisvaderJ. E.LindemanG. J.2008Cancer stem cells in solid tumours: accumulating evidence and unresolved questionsNat Rev Cancer, 10Oct and 2008), 755768
  64. 64. WangZ.LiY.BanerjeeS.SarkarF. H.2009Emerging role of Notch in stem cells and cancerCancer Lett, 1Jun 28 and 2009), 812
  65. 65. WatanabeK.BiancoC.StrizziL.HamadaS.MancinoM.BaillyV.MoW.WenD.MiatkowskiK.GonzalesM.SanicolaM.SenoM.SalomonD. S.2007aGrowth factor induction of Cripto-1 shedding by glycosylphosphatidylinositol-phospholipase D and enhancement of endothelial cell migration.J Biol Chem, 43Oct 26 and 2007a), 3164331655Print)
  66. 66. WatanabeK.HamadaS.BiancoC.MancinoM.NagaokaT.GonzalesM.BaillyV.StrizziL.SalomonD. S.2007bRequirement of glycosylphosphatidylinositol anchor of Cripto-1 for trans activity as a Nodal co-receptor.J Biol Chem, 49Dec 7 and 2007b), 3577235786Print)
  67. 67. WatanabeK.MeyerM. J.StrizziL.LeeJ. M.GonzalesM.BiancoC.NagaokaT.FaridS. S.MargaryanN.HendrixM. J.VonderhaarB. K.SalomonD. S.2010Cripto-1 is a cell surface marker for a tumorigenic, undifferentiated subpopulation in human embryonal carcinoma cellsStem Cells8Aug and 2010), 13031314Electronic)
  68. 68. WatanabeK.NagaokaT.LeeJ. M.BiancoC.GonzalesM.CastroN. P.RangelM. C.SakamotoK.SunY.CallahanR.SalomonD. S.2009Enhancement of Notch receptor maturation and signaling sensitivity by Cripto-1J Cell Biol, 3Nov 2 and 2009), 343353
  69. 69. WechselbergerC.EbertA. D.BiancoC.KhanN. I.SunY.Wallace-JonesB.MontesanoR.SalomonD. S.2001Cripto-1 enhances migration and branching morphogenesis of mouse mammary epithelial cellsExp Cell Res, 1May 15 and 2001), 95105
  70. 70. WechselbergerC.StrizziL.KenneyN.HirotaM.SunY.EbertA.OrozcoO.BiancoC.KhanN. I.Wallace-JonesB.NormannoN.AdkinsH.SanicolaM.SalomonD. S.2005Human Cripto-1 overexpression in the mouse mammary gland results in the development of hyperplasia and adenocarcinoma.Oncogene25Jun 9 and 2005), 40944105
  71. 71. WeiC. L.MiuraT.RobsonP.LimS. K.XuX. Q.LeeM. Y.GuptaS.StantonL.LuoY.SchmittJ.ThiesS.WangW.KhrebtukovaI.ZhouD.LiuE. T.RuanY. J.RaoM.LimB.2005Transcriptome profiling of human and murine ESCs identifies divergent paths required to maintain the stem cell state.Stem Cells, 2Feb and 2005), 166185
  72. 72. WilsonA.RadtkeF.2006Multiple functions of Notch signaling in self-renewing organs and cancerFEBS Lett, 12May 22 and 2006), 28602868Print)
  73. 73. XingP. X.HuX. F.PieterszG. A.HosickH. L.Mc KenzieI. F.2004Cripto: a novel target for antibody-based cancer immunotherapy.Cancer Res, 11Jun 1 and 2004), 40184023
  74. 74. XuC.LiguoriG.PersicoM. G.AdamsonE. D.1999Abrogation of the Cripto gene in mouse leads to failure of postgastrulation morphogenesis and lack of differentiation of cardiomyocytes.Development, 3Feb and 1999), 483494Print)
  75. 75. YanY. T.LiuJ. J.LuoY.E. C.HaltiwangerR. S.Abate-ShenC.ShenM. M.2002Dual roles of Cripto as a ligand and coreceptor in the nodal signaling pathwayMol Cell Biol, 13Jul and 2002), 44394449Print)
  76. 76. YeungT. M.GandhiS. C.BodmerW. F.2011Hypoxia and lineage specification of cell line-derived colorectal cancer stem cellsProc Natl Acad Sci U S A, 11Mar 15 and 2011), 43824387Electronic)

Written By

Nadia Pereira Castro, Maria Cristina Rangel, Tadahiro Nagaoka, Hideaki Karasawa, David S. Salomon and Caterina Bianco

Submitted: 22 November 2010 Published: 15 September 2011