Targeting Tumor Perfusion and Oxygenation Modulates Hypoxia and Cancer Sensitivity to Radiotherapy and Systemic Therapies

Hypoxia, a partial pressure of oxygen (pO2) below physiological needs, is a limiting factor affecting the efficiency of radiotherapy. Indeed, the reaction of reactive oxygen species (ROS, produced by water radiolysis) with DNA is readily reversible unless oxygen stabilizes the DNA lesion. While normal tissue oxygenation is around 40 mm Hg, both rodent and human tumors possess regions of tissue oxygenation below 10 mm Hg, at which tumor cells become increasingly resistant to radiation damage (radiobiological hypoxia) (Gray, 1953). Because of this so-called “oxygen enhancement effect”, the radiation dose required to achieve the same biologic effect is about three times higher in the absence of oxygen than in the presence of normal levels of oxygen (Gray et al., 1953; Horsman & van der Kogel, 2009). Hypoxic tumor cells, which are therefore more resistant to radiotherapy than well oxygenated ones, remain clonogenic and contribute to the therapeutic outcome of fractionated radiotherapy (Rojas et al., 1992). Tumor hypoxia results from the imbalance between oxygen delivery by poorly efficient blood vessels and oxygen consumption by tumor cells with high metabolic activities. On the one hand, oxygen delivery is impaired by structural abnormalities present in the tumor vasculature (Munn, 2003). They include caliber variations with dilated and narrowed single branches of tumor vessels, non-hierarchical vascular networks, disturbed precapillary architecture, and incomplete vascular walls. These structural abnormalities cause numerous functional impairments, i.e. increased transcapillary permeability, increased vascular permeability, interstitial hypertension, and increased flow resistance (Boucher et al., 1996; McDonald & Baluk, 2002). It is however important to note that, although hastily formed immature tumor microvessels lack smooth muscle layer(s) and are therefore unable to provide autoregulation, it is not uncommon to find mature blood vessels with smooth muscle layers and neural junctions inside slow-growing tumors (e.g. most human tumors) (Feron, 2004). On the other hand, the altered tumor cell metabolism with elevated metabolic rates also contributes to the occurrence of hypoxic regions in tumors and further causes extracellular acidification. Tumor hypoxia occurs in two ways: chronic hypoxia (or diffusion-limited hypoxia), and acute hypoxia (or perfusion-limited or fluctuating hypoxia). Chronic hypoxia has classically been thought to result from long diffusion distances


Introduction
Hypoxia, a partial pressure of oxygen (pO 2 ) below physiological needs, is a limiting factor affecting the efficiency of radiotherapy. Indeed, the reaction of reactive oxygen species (ROS, produced by water radiolysis) with DNA is readily reversible unless oxygen stabilizes the DNA lesion. While normal tissue oxygenation is around 40 mm Hg, both rodent and human tumors possess regions of tissue oxygenation below 10 mm Hg, at which tumor cells become increasingly resistant to radiation damage (radiobiological hypoxia) (Gray, 1953). Because of this so-called "oxygen enhancement effect", the radiation dose required to achieve the same biologic effect is about three times higher in the absence of oxygen than in the presence of normal levels of oxygen (Gray et al., 1953;Horsman & van der Kogel, 2009). Hypoxic tumor cells, which are therefore more resistant to radiotherapy than well oxygenated ones, remain clonogenic and contribute to the therapeutic outcome of fractionated radiotherapy (Rojas et al., 1992). Tumor hypoxia results from the imbalance between oxygen delivery by poorly efficient blood vessels and oxygen consumption by tumor cells with high metabolic activities. On the one hand, oxygen delivery is impaired by structural abnormalities present in the tumor vasculature (Munn, 2003). They include caliber variations with dilated and narrowed single branches of tumor vessels, non-hierarchical vascular networks, disturbed precapillary architecture, and incomplete vascular walls. These structural abnormalities cause numerous functional impairments, i.e. increased transcapillary permeability, increased vascular permeability, interstitial hypertension, and increased flow resistance (Boucher et al., 1996;McDonald & Baluk, 2002). It is however important to note that, although hastily formed immature tumor microvessels lack smooth muscle layer(s) and are therefore unable to provide autoregulation, it is not uncommon to find mature blood vessels with smooth muscle layers and neural junctions inside slow-growing tumors (e.g. most human tumors) (Feron, 2004). On the other hand, the altered tumor cell metabolism with elevated metabolic rates also contributes to the occurrence of hypoxic regions in tumors and further causes extracellular acidification. Tumor hypoxia occurs in two ways: chronic hypoxia (or diffusion-limited hypoxia), and acute hypoxia (or perfusion-limited or fluctuating hypoxia). Chronic hypoxia has classically been thought to result from long diffusion distances www.intechopen.com Advances in Cancer Therapy 290 between tumor vessels as the consequence of the more rapid expansion of tumors cells than that of the supporting vasculature (Vaupel et al., 1989). It is now well established that steep longitudinal gradients of pO 2 along the vascular tree, as opposed to radial diffusion of oxygen, can largely contribute to deficiencies in tumor oxygen supply (Dewhirst et al., 1999). The origin of acute hypoxia in tumors is not firmly established. The commonly held view has been that acute hypoxia results primarily from vascular stasis, which stems from one of three causes: 1) vascular collapse in regions of high tumor interstitial pressure, 2) vessel plugging by leukocytes, and 3) impingement of tumor cells on the vascular lumen. It has been demonstrated that temporal instability in tumor red blood cell flux could lead to transient hypoxia , and Dewhirst linked temporal changes in microvessel red blood cell flux to changes in the oxygen content in the same vessel . Factors that may contribute to flow fluctuations include arteriolar vasomotion and rapid vascular modeling (Baudelet et al., 2004Dewhirst et al., 1996;Patan et al., 1996). More recent studies indicate a widespread presence of fluctuating hypoxia in solid tumors (Cardena-Navia et al., 2008). The effect of tumor hypoxia on the response to treatment by ionizing radiation has been demonstrated in a multitude of experimental studies. In a series of clinical studies in the early nineties, Vaupel and others showed d e f i n i t i v e l y t h a t m e a s u r e m e n t s o f p O 2 by polarographic microelectrodes provided useful criteria for predicting the response of tumors to radiation therapy (Gatenby et al., 1988;Hockel et al., 1993;Okunieff et al., 1993;Stone et al., 1993;Thomas et al., 1994). These results stimulated considerable efforts in defining and evaluating therapeutic approaches designed to overcome tumor hypoxia as source of resistance (Horsman & van der Kogel, 2009). A particular area under focus is thus to combine radiotherapy with treatments that increase tumor pO 2 . Other approaches consist to chemically radiosensitize hypoxic cells or alternatively to exploit hypoxia as a mean to selectively kill the resistant population of hypoxic cells. Before the advent of imaging methods able to provide non-invasively oxygen estimation, animal and clinical studies were generally designed to evaluate the effect of a given treatment on tumor pO 2 as measured by Eppendorf or histological markers of tumor hypoxia. The clinical end points were generally locoregional control and survival. Modifiers of oxygen delivery tested in clinical trials included hyperbaric oxygen therapy (HBO), oxygen and carbogen breathing. Hypoxic cell radiosensitizers (possessing a selective toxicity for the radioresistant hypoxic cells) tested in clinical trials included metronidazole, misonidazole, nimorazole, and tirapazamine. In a systematic review, J. Overgaard (2007) identified 10,108 patients in 86 randomized trials designed to modify tumor hypoxia in patients treated with curative attempted primary radiation therapy alone. Overall modification of tumor hypoxia significantly improved the effect of radiotherapy for the outcome of locoregional control and with an associated significant overall survival benefit. No significant influence was found on the incidence of distant metastases or on the risk of radiation-related complications. From this meta-analysis, the authors concluded in 2007 that "Ample data exist to support a high level of evidence for the benefit of hypoxic modification. However, hypoxic modification still has no impact on general clinical practice". Currently, the most advanced therapeutic interventions used in the clinic to target tumor hypoxia are either the DAHANCA (Danish head and neck cancer) trial, the application of the ARCON (Accelerated radiotherapy, carbogen and nicotinamide) protocol, and phase III studies with Tirapazamine. In the DAHANCA phase III study, nimorazole has been used as hypoxic radiosensitizer on 422 patients, and it was shown that this compound improves the www.intechopen.com Targeting Tumor Perfusion and Oxygenation Modulates  Hypoxia and Cancer Sensitivity to Radiotherapy and Systemic Therapies   291 effect of radiotherapeutic management in head and neck cancer (Overgaard et al., 1998). Since these results, nimorazole administration became part of the standard irradiation protocol for Head and Neck cancer in Denmark. However, these findings have had no impact on general clinical practice except for Denmark because earlier generations of these agents induced rather severe peripheral neuropathy and because nearly all of the individual phase III trials yielded negative or inconclusive results (Ang, 2010). The ARCON protocol consists in the combination of accelerated radiotherapy to overcome tumor cell proliferation, carbogen breathing to overcome diffusion-limited hypoxia, and nicotinamide to minimize capillary bed shutdown and thereby reduce perfusion-related acute hypoxia. Phase I and II clinical trials have shown the feasibility and tolerability of the treatment and have produced promising results in term of tumor control, in particular in cancer of the head and neck and bladder (Kaanders et al., 2002). A large improvement in survival was demonstrated using this approach during radiotherapy for bladder cancer. The randomized multicentre phase III trial, designed and coordinated at Mount Vernon Cancer Centre, demonstrated a 13% benefit in overall survival when radiotherapy was combined with carbogen and nicotinamide compared to radiotherapy alone (ASTRO, 2009). Results from a large phase III trial launched to test this regimen will become available within the next 2 years. Finally, Tirapazamine (TPZ) has attracted interest after preclinical studies showing that in addition to augmenting the cytotoxicity of both radiation and cisplatin, this compound selectively kills hypoxic cells (Rischin et al., 2001;. Phase I and II studies of the combination of TPZ with radiation and cisplatin were performed on patients with locally advanced head and neck carcinoma. On the basis of the phase II data, a large international phase III trial was launched (Peters et al., 2010). Surprisingly, the combination did not show any evidence of improvement in overall survival. Nevertheless, patients were not previously screened for tumor hypoxia, the study was multicentric with some centers enrolling fewer than five patients and a consequent decrease in the quality of radiotherapy planning and delivery which can have dramatic consequences on outcome (Ang, 2010). This chapter will explore 2 strategies to radiosensitize tumors to X-rays: to increase oxygen delivery by exploiting the reactivity of mature tumor vessels (the so-called 'provascular' approach) and to decrease oxygen consumption by tumor cells. The goal of the provascular approach is to temporarily increase tumor perfusion and oxygenation through pharmacological interventions. Accordingly, radiotherapy could benefit from tumor reoxygenation whereas a decrease in interstitial pressure could facilitate tumor accessibility to circulating drugs. Alternatively, a second approach is to decrease the oxygen consumption by tumor cells since theoretical modeling studies demonstrated that reducing O 2 consumption was far more efficient at reducing tumor hypoxia than increasing blood pO 2 or flow (Secomb et al., 1995). We will also describe attempts to combine both approaches that can be considered as complementary strategies. The evaluation and validation of these adjuvant therapies require imaging techniques capable to accurately monitor tumor perfusion and oxygenation. From the clinical analyses cited above, it also appeared that the variation in the results among the trials reflects a considerable heterogeneity among tumors and that patient individualization would be mandatory for the success of such therapeutic approach. There is therefore an essential need to predict individually the presence of hypoxic regions in tumors. Based on individual tumor characteristics and/or the ability to alleviate tumor hypoxia, it will become possible to adapt the individual treatment either by delivering optimal radiation doses into the resistant areas or by delivering an associated treatment for www.intechopen.com Advances in Cancer Therapy 292 potentiating the efficacy of radiation treatments. In the early nineties, invasive techniques such as polarographic electrodes have been used in clinical studies to definitely establish the value of hypoxia as a predictive marker of the response of tumors to irradiation. Although this method was successful in demonstrating the central role played by tumor hypoxia in the clinical response to radiation therapy, it has never been used in standard clinical practice because of its invasiveness and the difficulty to systematically carry out longitudinal studies in individual patients. Fortunately, it is now possible to estimate tumor oxygenation by using minimally or non invasive techniques. This will be the purpose of the last part of this chapter.

Improving oxygen delivery to the tumor: The provascular approach
Tumors are highly heterogeneous and this heterogeneity extends to the tumor vasculature (see introduction). Beside neovessels that are the target of anti-angiogenic agents, human and rodent tumors also contain blood vessels that are structurally mature (Mattson et al., 1978;Peterson & Mattson, 1984). These vessels possess the minimal contractile features (such as pericytes or vascular smooth muscle cells) endowing them with vasocontractile properties. The intrinsic reactivity of tumor-feeding vessels modulates oxygen delivery and the accessibility of circulating drugs to the tumor. A selective and transient dilation of these vessels should thus improve the tumor response to radiotherapy (which depends on tumor oxygenation) and chemotherapy (which depends on perfusion and on the vascular exchange area). We termed this approach 'provascular' to contrast with antivascular and antiangiogenic approaches that are destructive by nature (Sonveaux, 2008). The net effect of systemic vasodilation on tumor pO 2 is unpredictable because it primarily depends on the arrangement of vessels (in series or in parallel) between the tumor and surrounding host tissues (Zlotecki et al., 1995). The key issue to resolve is thus to identify tumor-selective vasodilators. Treatment optimization would also require to monitor on individual bases the tumor response to treatment, preferentially using early surrogate, predictive and noninvasive markers.

Nitric Oxide (NO) and endothelin-1 (ET1) related strategies
Physiologically, the vascular tone is determined by the balance between nitric oxide (NO, a potent vasodilator) and endothelin-1 (ET1, a potent vasoconstrictor) (Sonveaux & Feron, 2005a). A number of studies have explored the functionality and the provascular exploitability of these 2 systems, as described below.

Exogenous and endogenous NO
NO was initially investigated for its vasodilatory activity and NO-donors were anticipated to improve the therapeutic efficacy of chemo-and radiotherapy upon combinational delivery (Sonveaux et al., 2009). We first considered the effect of the application of exogenous NO on tumor hemodynamic parameters and radiation response. This was performed by systemic administration of NO donor compounds, including isosorbide dinitrate (Jordan et al., 2000), Xanthinol Nicotinate (Segers et al., 2010), and S-nitrosocaptopril (Jordan et al., 2010a). The stimulation of the production of endogenous NO was also achieved by administration of insulin . All treatments resulted in a transient acute improvement of experimental tumor oxygenation with a consecutive increase in tumor radiosensitivity upon sequential administration of X-rays during the www.intechopen.com Targeting Tumor Perfusion and Oxygenation Modulates Hypoxia and Cancer Sensitivity to Radiotherapy and Systemic Therapies 293 reoxygenation window identified for each tumor model (Jordan et al., 2010a). The reoxygenation effect was shown to be due to an increase in tumor blood flow for Isosorbide Dinitrate, Xanthinol Nicotinate and S-nitrosocaptopril, using either dynamic contrastenhanced magnetic resonance imaging (DCE-MRI), where the number of perfused voxels and/or Ktrans, Kep, or Vp parameters was increased (see 5.2.1) , or patent blue staining (Jordan & Gallez, 2010b). Importantly, for some co-treatments, the increase in blood flow occurred concomitantly with a decrease in the rate of oxygen consumption by tumor cells. Inhibition of tumor cell respiration is the main mechanism accounting for insulin-induced tumor reoxygenation (see below). Endogenous NO is produced by a series of enzymes collectively termed NO-synthases (NOS). The endothelial isoform, eNOS, is adapted for the local stimulation of vasodilation following a response to stimuli that release calcium from intracellular stores and promote a calcium-calmodulin-dependent release of eNOS from its inhibitory complex with caveolin-1 (Cav-1) (Arnold et al., 1977;Michel et al., 1997). This mode of activation allows the transient production of micromolar amounts of NO responsible for vasodilatation. Using myography, we showed that this system is insensitive to classical eNOS stimulators (such as acetylcholine) selectively in tumor arterioles, thus suggesting that strategies able to restore eNOS activity would selectively target tumor vessels . Among different treatments, we have found that ionizing radiations themselves were able to restore the normal vasodilatory properties of tumor vessels. X-rays, through the production of reactive oxygen species (ROS), indeed induce an increase in eNOS expression concomitantly with a decrease in Cav-1 expression, which removes a functional brake promoting eNOS activation (Sonveaux et al., , 2009. Irradiations further stimulate NO production through the ROS-dependent activation of the PI3 kinase pathway, a well described pathway supporting Akt-mediated eNOS phosphorylation (on Ser1177, human sequence) and activation (Sonveaux et al., 2003(Sonveaux et al., , 2007a. We documented that radiation-induced vasodilation takes an active part in the antitumor effects of X-rays by showing that eNOS inhibition between the first and second irradiation of a clinical regimen of fractionated radiotherapy results in the total loss of the antitumor efficacy of the second dose, whereas eNOS inhibition before a single dose does not preclude cytotoxic effects . Active vasodilation after each of the consecutive doses of fractionated radiotherapy is associated with a window of tumor reoxygenation that offers a scientific rationale for the clinical use of radiotherapy in its fractionated mode.

S-nitrosylated hemoglobin and nitrites
A smart delivery of exogenous NO would help to resolve the Steal Effect, a process through which systemic vasodilation may in fact reduce tumor perfusion and oxygenation by redirecting blood to normal blood vessels that are generally more sensitive to vasoactive treatments and constitute a denser network (Zlotecki et al., 1995). Using hemoglobin (Hb) is an interesting approach because Hb is a physiological NO carrier (in the form of Snitrosothiol) poised to deliver NO selectively in hypoxic tissues such as tumors (Sonveaux et al., 2005b). NO delivery, indeed, is possible only after the conformational change associated with Hb deoxygenation (Jia et al., 1996;McMahon et al., 2002;Stamler et al., 1997). Using cell-free human S-nitrosylated Hb (SNO-Hb) in rats, we documented a transient increase in tumor perfusion, but only when SNO-Hb was delivered in oxygenated blood (i.e., intraarteriolar injection or intravenous injection concomitantly with carbogen breathing) (Sonveaux et al., 2005b). In deoxygenated blood, SNO-Hb would otherwise readily deoxygenate and release NO at the site of delivery. While increased tumor perfusion at low dose SNO-Hb is primarily attributable to central effects (i.e., baroreceptor inhibition), SNO-Hb at higher doses could act as a tumor-selective vasodilator and could therefore be used as a radiosensitizing treatment. Inhalation of the NO-donor gas ethyl nitrite, which promotes the S-nitrosylation of intra-erythrocytic Hb in the lungs, could have the same effects while minimizing toxic side effects associated with the administration of naked Hb (Moya et al., 2002;Sonveaux et al., 2007b). While the use of SNO-Hb exploits hypoxia as a mean to selectively deliver NO to tumors, one can also take advantage of the low pH coupled to the high metabolic activities of many solid tumors. Nitrites for example can be reduced to NO either by enzymatic catalysis (nitrite reductase activities of xanthine oxidase, eNOS and Hb) or by non enzymatic disproportionation, and these processes are facilitated in an acidic microenvironment (Angelo et al., 2006;Godber et al., 2000;Modin et al., 2001;Vanin et al., 2007;Zweier et al., 1999). They have been used clinically as an antidote for cyanide poisoning (Holland & Kozlowski, 1986), which also indicates that they can be safely administrated to humans. We therefore tested whether the low pH of tumors (on average pH 6.7) could be exploited to generate NO from nitrites selectively in tumors. We observed ex vivo that nitrite-induced vasodilation was more pronounced at pH 6.7 compared to pH 7.4 (Frerart et al., 2008). We also found that the bioactivity of nitrites at low pH encompassed NO-mediated inhibition of tumor cell respiration, which indicates that the robust and transient increase in tumor pO 2 after nitrite delivery to mice is the result of the combination of vasoactive and metabolic responses. When administered to reach a plasma concentration of 100 µM in mice, nitrites sensitized tumors to radiotherapy (Frerart et al., 2008). Further clinical applications are however confronted to financial issues: clinical trials are now warranted whereas nitrites or their use in cancer therapy can not be patented.

Endothelin-1 inhibitors
Endothelin-1 (ET-1) is a strong vasoconstrictor and an autocrine growth factor produced by tumor cells (Haynes & Webb, 1994;Shichiri et al., 1991). It has a key role in the accommodation of vasoactive blood vessels to variations in intraluminal pressure: ET-1 mediates the myogenic tone, a vasoconstriction that buffers perfusion changes when the blood pressure increases (Huang & Koller, 1997). In tumors, the constant exposure of arterioles to ET-1 in vivo results in an increased myogenic tone that can be detected ex vivo . We reasoned that it constituted a reserve for vasorelaxation that could be exploited to sensitize tumors to radio-and chemotherapy. ET-1 induces vasoconstriction when binding to ET A receptors expressed by contractile vascular cells (Maguire & Davenport, 1995). Using the ET A antagonist BQ123, we observed ex vivo a vasodilation selectively in tumor vessels (compared to size-matched vessels from nonmalignant tissues) that translated in vivo into increased tumor perfusion and oxygenation . Both responses were tumor-selective and transient. BQ123 as a pretreatment therefore improved the antitumor effects of X-ray radiotherapy and cyclophosphamide (after systemic delivery) Sonveaux et al., 2004).

Normalization effect of anti-angiogenic agents
Given that anti-angiogenic agents will likely be combined with radiation therapy, it is critical to understand alterations in tumor oxygenation and perfusion, as well as to define www.intechopen.com Targeting Tumor Perfusion and Oxygenation Modulates Hypoxia and Cancer Sensitivity to Radiotherapy and Systemic Therapies 295 optimal time points for the delivery of radiation. Our group previously studied the modifications in the tumor environment early after treatment with the anti-angiogenic agent thalidomide, with a special focus on a possible normalization of the tumor vasculature (Jain, 2001;Tong et al., 2004) that could be beneficial for radiotherapy. Our results showed an increase in tumor pO 2 during the first 2 days of thalidomide treatment, which was likely the result of the ability of thalidomide to modify tumor microenvironmental parameters such as the vascular supply and tumor perfusion, as shown by DCE-MRI (see 5.2.1) and histological analysis using the endothelial marker CD31 (Ansiaux et al., 2005). Indeed, the histological analysis revealed profound modifications in the vascular supply: a reduction in the number of tumor microvessels after thalidomide treatment together with a dilation of the remaining vessels with no decrease in the tumor vascular density. The perfusion measured by DCE-MRI showed an increased plasma volume fraction (see 5.2.1), which could be explained by the shift to larger blood vessel diameters as observed in histology analysis, perhaps due to compensation for the loss of small vessels. Interestingly, similar observations were not obtained using more specific anti-angiogenic agents such as SU-5416 or ZD-6474 . For these compounds, tumor reoxygenation was rather due to a decrease in the rate of oxygen consumption by tumor cell and no normalization effect was observed in the tumor models under study (see below). We hypothesized that specific inhibition of vascular endothelial growth factor (VEGF) signaling via VEGFR2 by SU-5416 or ZD-6474 may have been compensated by another angiogenic pathway such as basic fibroblast growth factor (bFGF), platelet-derived growth factor (PDGF), transforming growth factor (TGF)-, or Tie-2 signaling (Folkman et al., 2001;Stratmann et al., 1998); contrary to thalidomide which acts on different angiogenic pathways. It is nevertheless important to note that these findings are specific to the tumor models under study, since ZD-6474 was described earlier to be able to decrease both flow and permeability in human colon tumors (Bradley et al., 2008) and was able to induce transient normalization of the vasculature in gliomas (Claes et al., 2008).

Decreasing oxygen consumption by tumor cells
Tumor oxygenation is a matter of supply and demand. Whereas the provascular strategy intends to improve oxygen supply, several strategies are aimed at decreasing oxygen consumption by tumor cells rendering molecular O 2 available for the stabilization of radiation-induced DNA damage. Indeed, theoretical modeling studies demonstrated that reducing O 2 consumption could be more efficient at reducing tumor hypoxia than increasing blood pO 2 or flow (Secomb, 1995). Two main targets can be considered for inhibiting oxygen consumption: (i) direct interference with the mitochondrial respiratory chain (at different levels), and (ii) modulation of the redox status to change the mitochondrial membrane potential (Pilkington et al., 2008); the final aim being a subsequent increase in tumor pO 2 and enhancement of the efficacy of radiotherapy. In contrast to provascular strategies, Laser Doppler flowmetry, DCE-MRI and electron paramagnetic resonance (EPR) oximetry have revealed that the radiosensitizing effects of these treatments are primarily caused by a decrease in the rate of oxygen consumption by tumor cells, thus allowing oxygen to be redirected from a metabolic fate to the stabilization of DNA lesions. Indeed, apart from NO donors, all the treatments described below did not show any significant increase in tumor blood flow concomitant to the increase in tumor oxygenation. Some of them even showed a decrease in tumor blood flow that was counteracted by the dramatic decrease in oxygen consumption by tumor cells (i.e. insulin and NS-398). In addition, regarding NO-mediated treatments, our models showed that the radiotherapeutic response not only depended on the tumor pO 2 but also on the net level of NO achieved at the time of irradiation, NO itself being able to stabilize irradiation-induced DNA lesions in vivo . The first drug that was described to inhibit oxygen consumption in tumors was metaiodobenzylguanidine (MIBG), which causes an inhibition of the mitochondrial site I electron transfer, inhibition of NAD(P)H oxidation, and is described to alter tumor glycolysis by inhibiting oxygen consumption (Biaglow et al., 1998). We consecutively focused on different innovative treatments that may alter oxygen consumption by tumor cells, as listed below.

Insulin
This hormone was known to increase blood flow in human skeletal muscle and was postulated to be an important modulator of tumor oxygenation . Indeed, we showed that insulin had a profound effect on tumor oxygenation that was not due to an increase in tumor blood flow but to a decrease in tumor cell oxygen consumption. The increase in tumor oxygenation resulted in an important enhancement in the sensitivity of tumors to irradiation. The likely scenario involves a stimulation of eNOS and a consequent increase in NO release. As NO regulates mitochondrial respiration by virtue of reversible interactions with cytochrome c oxidase (complex IV), an increase in NO release consequently decreased cell respiration . A preclinical study confirmed the dose-dependant increase in tumor oxygenation and radiation sensitivity by insulin, without any increase in the radiation toxicity for normal tissues (Jordan et al., 2006a).

Glucocorticoids
Earlier work had demonstrated that the administration of cortisone to rats resulted in both the inhibition of oxygen consumption and the uncoupling of oxidative phosphorylation in liver mitochondria (Kimberg et al., 1968). Glucocorticoids seemed to decrease the cytochrome c oxidase (complex IV) activity of isolated rat kidney mitochondria by a direct mechanism (Simon et al., 1998). Our group showed an important increase in tumor oxygenation induced by an effect on oxygen consumption. Decreased oxygen consumption could be explained by the capacity of glucocorticoids to inhibit cytochrome c oxidase of the mitochondrial respiratory chain. The result of this increase in tumor oxygenation was an improvement of the radiation efficacy by a factor of 1.7 .

Anti-inflammatory drugs
Several reports indicated that many non-steroidal anti-inflammatory drugs (NSAIDs) uncouple mitochondrial oxidative phosphorylation with important consequences on cell oxygen consumption. However, it was suggested that the response was dependent on the dose as well as on the type of NSAIDs. For the first time, our group reported that the administration of NSAIDs induced a dramatic increase in tumor oxygenation explained by reduced oxygen consumption. An increase in the tumor response was observed when the irradiation was applied at the time of maximal reoxygenation (Crokart et al., 2005).

Thyroid hormones
Chronic alteration in the thyroid status has been shown to affect mitochondrial oxygen consumption in skeletal muscle (Gredilla et al., 2001). Also, studies have demonstrated that www.intechopen.com Targeting Tumor Perfusion and Oxygenation Modulates Hypoxia and Cancer Sensitivity to Radiotherapy and Systemic Therapies 297 hypothyroidism slows down the neoplastic process, whereas administration of a thyroid hormone preparation restores tumor growth rates (Mishkin et al., 1981;Shoemaker & Dagher, 1979;Theodossiou et al., 1999). In humans, several case reports have indicated a prolonged survival in the presence of hypothyroidism (Cristofanilli et al., 2005;Hercbergs & Leith, 1993). Moreover, a decrease in the thyroid function may also serve to favorably influence the response to treatment. Finally, patients presented an enhanced response rate to chemotherapy and survived significantly longer under hypothyroidism (Hercbergs et al., 2003). Our group recently demonstrated that the thyroid status is associated with a significant change in tumor radiosensitivity since the regrowth delay was increased in hypothyroid mice compared to euthyroid mice. Mechanistically, we demonstrated that the higher level of tumor oxygenation in hypothyroid mice results from a significant reduction in the oxygen consumption rate of tumors .

NO donors
We recently tested whether S-nitrosocaptopril, a molecule combining a NO donor and an angiotensin converting enzyme inhibitor (ACE inhibitor), could temporarily improve the hemodynamic status of experimental tumors. We identified a time window during which tumor oxygenation was improved, as a result of a combined effect on tumor blood flow and oxygen consumption. Consequently, the administration of S-nitrosocaptopril contributed to the increase in efficacy of radiation therapy, an effect that was not observed with captopril alone (Jordan et al., 2010a).

Anti-angiogenic agents
As stated earlier, two anti-angiogenic agents, SU-5416 and ZD-6474, have also been identified as potent inhibitors of oxygen consumption (Ansiaux et al., 2007(Ansiaux et al., , 2009). Our major findings regarding those specific anti-angiogenic agents were the following: (a) SU-5416 and ZD-67474 both induce an increase in tumor oxygenation at an early phase of treatment (after 2 days of daily injections); (b) this tumor reoxygenation can be exploited to increase the efficacy of combined radiotherapy; (c) the mechanism of increase in tumor oxygenation does not involve a ''normalization'' of the tumor vasculature as described previously for thalidomide in the same tumor model (Ansiaux et al., 2005) but is consistent with the decrease in the rate of oxygen consumption by the tumor cells. Indeed, at this early stage of the treatment, no apparent remodeling of the tumor vasculature and no changes in tumor perfusion and permeability parameters were observed, using histological and DCE-MRI analysis, respectively. We however demonstrated a reduction in tumor oxygen consumption after those treatments. The reduction factor in oxygen consumption observed was sufficient to abolish tumor hypoxia, as we reported previously using the treatments listed above.

Hyperthermia: Combining provascular and oxygen consumption effects in a single treatment
Hyperthermia is a potent adjuvant therapy with radiotherapy and chemotherapy, and the perfect illustration of a strategy combining transient, local vasodilatation with the inhibition of tumor cell respiration. The heat treatment consists of elevating the temperature of tumors to a supra-physiological range of 40°C to 45°C at which tumor reoxygneation occurs with limited skin toxicity. Hyperthermia induces a graded response in tissues characterized by decreased oxygen consumption at temperatures ≥ 40°C, vasodilatation between 41°C and 41.5°C, and vascular damage above 42°C. Although direct tumor cell killing was demonstrated in vitro at higher temperatures, long-term tumor control has never been demonstrated using hyperthermia as the sole treatment modality. Vasodilation only modestly contributes to tumor reoxygenation at the low thermal doses. Increased pO 2 rather primarily results from changes in oxygen consumption in the target cells, and at least two different processes have been identified to contribute to this response. It is now well demonstrated that an important target of heat is proteins among which enzymes of the respiratory chain are more sensitive to heat inactivation/denaturation than glycolytic enzymes (Lepock et al., 1987;Kelleher et al., 1995). But the inhibition of mitochondrial respiration by heat lasts longer than the turnover time of respiratory enzymes, suggesting the existence of an additional mechanism. Dewhirst in collaboration with our group (Moon et al., 2010) recently demonstrated that mild hyperthermia activates the transcription factor hypoxia-inducible factor 1 (HIF-1) through an hypoxia-independent mechanism involving the sequential activation of Extracellular signal-Regulated Kinases (ERK) by heat shock, ERK-induced upregulation of the expression of the Nox1 subunit of NAD(P)H oxidase, increased ROS production by NAD(P)H oxidase, ROS-induced HIF-1 protein stabilization, and, ultimately, HIF-1 activation. HIF-1 target genes include most glycolytic enzymes and transporters as well as major pro-angiogenic molecules such as VEGF. Among these genes, we showed that pyruvate dehydrogenase kinase 1 (PDK1) largely mediates the inhibition of mitochondrial respiration by heat in tumor cells through inhibiting pyruvate dehydrogenase (PDH), i.e., the enzyme coupling glycolysis to the tricarboxylic acid (TCA) cycle (Moon et al., 2010). Furthermore, consistent with the increase in VEGF expression that we also observed in heat-treated tumors, we documented an increased vascular density in perfused tumor areas where oxygen is extracted from the blood. Tumor reoxygenation by mild hyperthermia is thus a multifaceted process involving the combination of decreased O 2 consumption by tumor cells and increased O 2 delivery by blood vessels. This and the fact that reoxygenation occurs at thermal doses lower than those inducing vascular damage justifies the use of mild hyperthermia as a combination treatment notably with radiotherapy. Although several clinical trials have confirmed that combining heat and radiotherapy is indeed associated with better patient treatment outcome (Brizel et al., 1996;Jones et al., 2003Jones et al., , 2005Vujaskovic et al., 2003), the future clinical development of hyperthermia strongly relies on designing tools allowing for homogeneous thermal dose distribution and improving imaging techniques able to correlate thermal maps of tumors to the clinical outcome of patients .

Non invasive imaging of tumor oxygenation and perfusion
The study of magnetic resonance (MR) markers over the past decade has provided evidence that the tumor microenvironment and hemodynamics play a major role in determining therapy outcome. Therefore, the identification of relevant non-invasive imaging endpoints is of crucial importance in the management of cancer patients. Improvement of the therapeutic index was evidenced in numerous preclinical studies that used multimodal imaging. The impact of non-invasive imaging in oncology extends from guiding preclinical development of targeted biomarkers and therapeutic agents, to assisting in the diagnosis and staging of tumors in the clinic, as well as monitoring the therapeutic response.

Tumor oxygenation measurements
There is a critical need for developing dynamic, non-invasive methods for direct oxygen mapping in the clinical practice. Although hypoxia is recognized as a crucial issue in many www.intechopen.com Targeting Tumor Perfusion and Oxygenation Modulates Hypoxia and Cancer Sensitivity to Radiotherapy and Systemic Therapies 299 disorders and in treatment response, the lack of easy-to-use and efficient methods to quantify oxygen deprivation hampers further pathophysiological understanding and restricts the clinical implementation of oxygen mapping techniques resulting in the absence of gold standard for measuring hypoxia in the day-to-day practice (Tatum et al., 2006). Below is a non exhaustive review of the most relevant non invasive methods able to assess tumor hemodynamic parameters. Methods to measure absolute pO 2 mostly encompass EPR oximetry and 19 F relaxometry whereas indirect methods include Blood Oxygen Level-Dependent (BOLD) MRI, Oxygen enhanced relaxation MRI, Oxygen enhanced longitudinal relaxation MRI and positron emission tomography (PET) tracers retained in hypoxic regions. Of note, our group has also developed innovative methods to assess tumor oxygen consumption in vitro and in vivo, which have been reviewed elsewhere (Jordan & Gallez, 2011).

Electron Paramagnetic Resonance (EPR) oximetry
EPR is a MR method that detects only species containing unpaired electrons (Gallez & Swartz, 2004a). One of the numerous applications of EPR is in vivo oximetry. Molecular oxygen is a triplet radical that possesses two unpaired electrons which are responsible for its paramagnetism. However, EPR is not able to detect oxygen itself when dissolved in fluids near room temperature: in biological systems, the output signal lines are so broadened as to be undetectable. Indirect methods exist. Most of these methods rely on the paramagnetic properties of molecular oxygen, which acts as an efficient relaxer for other paramagnetic species (Gallez et al., 2004b). The enhancement of relaxation rates scales linearly with the concentration of oxygen over a wide range of oxygen tensions. The lack of detectable levels of endogenous paramagnetic species makes it necessary to use exogenous paramagnetic materials. Variations in pO 2 of less than 1mmHg can be detected using particulate materials. While EPR spectroscopy provides local measurements, EPR imaging techniques provide spatially resolved measurements of these materials. The spatial distribution of free radicals can be performed utilizing magnetic field gradients in a manner similar to that of MRI. Spectral-spatial EPR imaging encodes both the spatial distribution of the spin probe and the spectral information, which allows the mapping of molecular oxygen (Kuppusamy et al., 2003). For this purpose, the use of soluble EPR materials such as trityl radicals is more convenient as they can diffuse in the whole tissue. EPR oximetry was compared with other methods that provide direct or indirect measurements of tumor oxygenation: with polarographic electrodes, the distribution of nitroimidazoles, the BOLD effect in MRI, and pO 2 recordings using OxyLite (reviewed in Gallez et al., 2004b). Two major challenges are now considered for moving this technology into the clinic: (i) assuring biocompatibility of the oxygen sensors in humans and (ii) modifying the instruments so that they can be used for humans instead of small animals (Swartz et al., 2004).

5.1.2
19 F relaxometry 19 F NMR spectroscopy and imaging of perfluorocarbon (PFC) emulsions (hydrocarbons with protons having been replaced with fluorine nuclei) has been extensively exploited to measure the oxygen tension of biological systems in preclinical studies. The 19 F MR signal of the PFC is sensitive to the pO 2 of the surrounding tumor tissue, and acts as an oximeter. The principle behind 19 F MR oximetry relies on the linear increase of the NMR spin-lattice relaxation rate R 1 (=1/T 1 ) of PFC emulsions with increasing oxygen tension (Mason et al. 1996). 19 F MR oximetry provides a sensitive measure of tissue oxygen tension and is a powerful approach for monitoring tumor hypoxia. Several PFCs have been used for NMR oximetry, but hexafluorobenzene (HFB) is preferred (Mason et al., 1996;Zhao, et al., 2004) because it has a six-fold symmetry with a single 19 F NMR resonance, and a low sensitivity to temperature. Its spin lattice relaxation rate is highly sensitive to pO 2 and exhibits a linear relationship across the entire range of tissue oxygenation. Mason and colleagues have been successfully developing fluorocarbon relaxometry using echo planar imaging for dynamic oxygen mapping (FREDOM) MRI following direct intratumoral injection of the oxygen reporter molecule HFB. Our group further developed an MRI fluorocarbon oximetry technique using snapshot inversion recovery with an improved temporal resolution of 1.5 minutes (vs. 6.5 minutes for FREDOM) ). Our method therefore provides a rapid way to map tumor oxygenation and is particularly suitable to monitor acute changes of pO 2 in tumors, including spontaneous fluctuations Magat et al., 2010). The translation to the clinic is currently limited by the lack of development of coils in the clinical setting, and the lack of characterization of PFCs in humans.

Blood Oxygen Level Dependent (BOLD) MRI
Functional MRI (fMRI) was first developed as an indirect method of imaging brain activity at high temporal resolution (Ogawa et al., 1990). The relative decrease in deoxyhemoglobin concentration, which has a paramagnetic effect, can be detected by MRI as a weak transient rise in the T 2 * weighted signal. This is the BOLD contrast principle. Apart from its very large application in neuroscience, the use of BOLD contrast in tumors brought with it new challenges of understanding and interpretation. Since then, BOLD MRI has become a useful tool for addressing important questions regarding the pathophysiology of tumors. However, it has both advantages and disadvantages. One advantage of BOLD MRI is that it is noninvasive and can be used to monitor real time changes of tumor oxygenation during pharmacological treatments or to monitor spontaneous fluctuations in experimental tumors (Baudelet & Gallez 2002;Baudelet et al., 2004). It does not require externally administered contrast medium or radioactive isotopes, it can be repeated as necessary, and flow dependence can be decoupled. BOLD MRI, in combination with hypercapnia and hyperoxia, is also an attractive method for assessing maturation and the functional state of tumor blood vessels . As for disadvantages, BOLD MRI is unfortunately a nonquantitative method for monitoring tumor pO 2 . This is the result of the extreme sensitivity of changes in R 2 * to the basal state of tumor oxygenation and blood volume fraction. The intra and intertumoral distribution of these parameters may be greatly heterogeneous, making it very difficult to compare estimated pO 2 changes between two regions or individuals. Even more problematic is the fact that the change in R 2 * is not always indicative of the change in pO 2 . Concomitant changes in blood volume, blood pH and metabolic status can lead to smaller-than-expected or even negative changes in R 2 * (Baudelet & Gallez, 2002). Similarly, changes in oxygen consumption rate has been described to result in a lack of change in R 2 * even though absolute pO 2 is increased (Jordan et al., 2006b).

Oxygen enhanced longitudinal relaxation MRI
An alternative MRI technique for evaluating change in tumor oxygenation using endogenous contrast relies in the increase of the proton longitudinal relaxation rate (R 1 ) of www.intechopen.com Targeting Tumor Perfusion and Oxygenation Modulates  Hypoxia and Cancer Sensitivity to Radiotherapy and Systemic Therapies   301 water containing oxygen, due to the paramagnetic properties of oxygen. The measured change in R 1 is, in theory, proportional to the change in tissue oxygen concentration (O'Connor et al., 2007(O'Connor et al., , 2009. Studies have indeed demonstrated that oxygen-enhanced MRI produces measurable signal changes in normal tissues in patients and is feasible on conventional clinical scanners. Therefore, oxygen-induced increase in R 1 has the potential to provide noninvasive measurements of change in tumor oxygen concentration, distinct from BOLD imaging. Nevertheless, the technique still lacks in sensitivity and the measured delta R 1 may include errors resulting from changes independent of tissue oxygen content, such as alteration in blood flow or tissue H 2 O content (O'Connor et al., 2009).

Hypoxia assessed by Positron Emission Tomography (PET)
18 F-labeled fluoromisonidazole ( 18 F-MISO) is probably the most widely used PET imaging agent for hypoxia. 18 F-MISO accumulates in tissues by binding to intracellular macromolecules when pO 2 < 10 mm Hg. Retention within tissues is dependent on nitroreductase activity (that is, on the reduction status of a NO 2 group on the imidazole ring) and accumulation in hypoxic tissues over a range of blood flows has been observed (Tatum et al., 2006). 18 F-MISO is only sensitive to the presence of hypoxia in viable cells: 18 F-MISO is not retained in necrosis because the electron transport chain that reduces the nitroimidazole to a bioreductive alkylating agent is no longer active (Padhani et al., 2007). Nevertheless, 18 F-MISO PET is able to monitor the changing hypoxia status of lung tumors during radiotherapy (Koh et al., 1995). Studies in sarcoma (Rajendran et al., 2003) and head and neck cancer (Rajendran et al., 2004) have demonstrated a correlation of 18 F-MISO uptake with poor outcome to radiation and chemotherapy. Other 18 F labeled nitroimidazoles are currently evaluated, including EF3 and fluoroazomycin arabinoside (FAZA), for example (Tatum et al., 2006).

Tumor perfusion measurements
Microvascular parameters such as permeability and perfusion are of particular interest in the context of the abnormal tumor microvascular network. Useful imaging systems have been developed to monitor angiogenesis and the microvasculature in vivo, including DCE-MRI (Choyke, et al. 2003), PET and Single Photon Emission Computed Tomography (SPECT), CT, Doppler ultrasound, and optical imaging methods (see Jennings, et al., 2008).

Dynamic Contrast Enhanced MRI
DCE-MRI consists in the acquisition of serial MR images before, during, and after the administration of an intravenous contrast agent (CA) to produce time series images that enable pixel-by-pixel analysis of contrast kinetics within a tumor. Pharmacokinetic models provide a means of summarizing contrast enhancement data in terms of parameters that relate to the underlying vascular anatomy and physiology. As described by Tofts et al. (1999), the essential features of a variety of models are covered by the generalized kinetic model. Most methods of analyzing dynamic contrast-enhanced T 1 -weighted data acquired with low molecular contrast medium use a compartmental analysis to obtain some combination of the three principal parameters: the transfer constant Ktrans in min -1 (volume transfer constant between blood plasma and ESS), the rate constant Kep in min -1 (rate constant between blood plasma and extravascular extracellular space [ESS]) and the volume of ESS per unit volume of tissue space, Vp (no unit). DCE-MRI has evolved from an experimental technique to a clinically feasible adjunct procedure that can be integrated into a standard morphologic imaging protocol. It does provide unique non-invasive functional information on the properties of tumors related to microcirculation (distribution volume, permeability, and perfusion). This information can improve diagnostic characterization, the follow-up of therapy, and tumor staging; and it provides tools to facilitate advanced molecular imaging. Preclinical and clinical studies suggest that a successful antivascular treatment results in a decrease in the rate of enhancement along with a decreased amplitude and a slower washout, and that poor response can result in persistent abnormal enhancement (Gillies et al., 2002).

Positron emission tomography
Generally, PET measures of tumor perfusion have used ( 15 O)-labeled radiotracers. The socalled steady state method requires inhalation of 15 O-CO 2 and the dynamic method requires an intravenous bolus injection of 15 O-H 2 O (Jennings et al., 2008). A requirement for quantification of perfusion using dynamic methods is an accurate determination of an arterial input function, which can be obtained non-invasively in a purely arterial region of interest, such as the aorta.

Computed tomography
In X-ray CT, the tissue contrast is based on variable attenuation coefficients of the object absorbing the X-rays. Hemodynamic parameters may be extracted from dynamic changes in X-ray attenuation caused by the intravenous injection of an iodinated contrast agent. Perfusion CT data can deliver quantitative hemodynamic information, such as blood volume, blood flow, permeability surface-area product and mean transit time (MTT) (Jennings et al., 2008).

Doppler ulstrasound
There are several different ultrasonic approaches designed specifically to measure blood flow including transit time, continuous-wave Doppler, pulsed and color Doppler, and power Doppler flowmeters, requiring the use of microbubbles (filled with air, perfluorocarbon, sulfur hexafluoride or nitrogen), which expand and contract because of pressure from the acoustical transmit pulse, and the primary mode of echogenicity is the impedance mismatch between the microbubble-blood interface, making them significantly more echogenic than normal tissue. Typical parameters that are estimated using Doppler ultrasound include: percent intratumor contrast agent uptake, enhancement timing and pattern, percent blood volume fraction, red blood cell velocity, and perfusion; depending on the type of study and tracer used (Jennings et al., 2008).

Conclusions
Heterogeneities in blood flow and oxygenation are key characteristics of solid tumors and constitute a therapeutic challenge when these tumors are treated with radiotherapy or systemic therapies. Because oxygen stabilizes DNA lesions, tumors become increasingly resistant to radiotherapy and to several forms of chemotherapy when the tumor pO 2 decreases below a threshold of 10 mmHg. In the past decades, basic and preclinical researches have identified several adjuvant treatments aimed at transiently increasing tumor oxygenation at the time of radiotherapy. Their identification was based on an increasing www.intechopen.com Targeting Tumor Perfusion and Oxygenation Modulates Hypoxia and Cancer Sensitivity to Radiotherapy and Systemic Therapies 303 understanding of the origins of tumor hypoxia, which logically opened two main avenues: co-treatments designed to (1) improve the oxygen supply from blood vessels at the time of radiotherapy (with different strategies such as increasing the O 2 content of blood, inducing tumor-specific vasodilation, or normalizing vascular structures), and (2) reduce the rate of O 2 consumption by tumor cells through metabolic interventions. Theoretical models now validated preclinically have revealed that the metabolic strategy has the highest impact on tumor radiosensitivity, but the best opportunity still resides in treatments combining both vascular and metabolic effects, as perfectly illustrated with hyperthermia. Most systemic anticancer treatments are also confronted to the difficulty to reach a target often located at distance from blood vessels, thus indicating that in this case increased tumor perfusion (i.e., decreased resistance to flow) could improve tumor bioavailability. NO-donors, ET-1 inhibitors, radiotherapy or heat as adjuvant provascular treatments, or anti-angiogenic therapies and chemotherapy used in a 'vascular normalization' mode, have all demonstrated their capacity to chemosensitize tumors in preclinical settings. Most of the adjuvant treatments described here could theoretically be exploited therapeutically by the off-label use of existing FDA-approved drugs, but it has also become evident that a given tumor in a given patient would respond differently than the tumor of the patient next-door. It is therefore urgent to develop and implement in the clinics imaging techniques able not only to provide predictive markers but also biological markers of the response to such combinational interventions. The MR and PET techniques that we reviewed here are among the most-sensitive non-invasive techniques having proved their highly valuable power as to measure changes in tumor perfusion and oxygenation preclinically. Current challenges include the FDA approval of exogenous tracers and sensors when needed, scaling-up tools initially dedicated for small laboratory animals and adapting imaging protocols to the clinical situation, the transfer to the clinics of the expertise needed for protocol design and data interpretation and, as importantly, a careful consideration of societal cost issues.