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Journal of Oncology
Volume 2010 (2010), Article ID 514310, 13 pages
The Role of Dysregulated Glucose Metabolism in Epithelial Ovarian Cancer
1Department of Biomedical Sciences, University of Guelph, Guelph, ON, N1G 2W1, Canada
2Department of Obstetrics and Gynecology, McMaster University, Hamilton, ON, L8S 4L8, Canada
3CIHR Group in Matrix Dynamics, University of Toronto, Toronto, ON, M5S 3E2, Canada
Received 29 April 2009; Accepted 3 December 2009
Academic Editor: Maurie M. Markman
Copyright © 2010 L. D. Kellenberger et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Epithelial ovarian cancer (EOC) is the most lethal gynecologic cancer and also one of the most poorly understood. Other health issues that are affecting women with increasing frequency are obesity and diabetes, which are associated with dysglycemia and increased blood glucose. The Warburg Effect describes the ability of fast-growing cancer cells to preferentially metabolize glucose via anaerobic glycolysis rather than oxidative phosphorylation. Recent epidemiological studies have suggested a role for hyperglycemia in the pathogenesis of a number of cancers. If hyperglycemia contributes to tumour growth and progression, then it is intuitive that antihyperglycemic drugs may also have an important antitumour role. Preliminary reports suggest that these drugs not only reduce available plasma glucose, but also have direct effects on cancer cell viability through modification of molecular energy-sensing pathways. This review investigates the effect that hyperglycemia may have on EOC and the potential of antihyperglycemic drugs as therapeutic adjuncts.
The poor survival statistics of epithelial ovarian cancer (EOC) are mentioned by way of introduction in almost all review literature pertaining to the disease. Unfortunately, in the past forty years there have been only small improvements in overall ovarian cancer survival rates. Specific challenges to the treatment of EOC include the problems of late detection, metastasis within the peritoneal cavity, drug resistance, and cancer recurrence even after initial response to treatment. Up to 90% of EOCs do not have an identified genetic component, and the development of specific and sensitive screening tools has proven elusive . A metabolic approach to the targeted treatment of EOC has the potential to address many of the issues that make this the most deadly gynecologic cancer.
In recent years, it has been noticed that the influence of lifestyle, in particular the high-fat Western diet, is associated with the multisite development of cancers. The state of chronic positive energy balance is linked to a cluster of conditions including impaired glucose regulation and insulin resistance, collectively called the metabolic syndrome . Hyperglycemia is a distinguishing feature of over-nutrition and it is believed to be an independent risk factor for cancer development. To provide an idea of the clinical importance of hyperglycemia, it is estimated that the incidence of type two diabetes mellitus (T2DM), a common consequence of the syndrome, will double in many regions in the next fifteen years. However, the burden of T2DM, where as many as one third of individuals are undiagnosed , almost certainly underestimates the true incidence of abnormal glucose homeostasis in the population. Given the emerging association between hyperglycemia and cancer, it is conceivable that there will be an increase in the incidence of EOC in the near future.
We hypothesize that hyperglycemia provides a nutrient-rich, growth signal-rich environment for epithelial ovarian cancer cells, where tumour formation and growth is encouraged by free radical-induced DNA damage. We address possible cellular mechanisms by which a hyperglycemic environment may increase the rate of development of ovarian tumours, and discuss the implications for metabolically targeted EOC treatments.
2. Hyperglycemia and EOC: Epidemiological Evidence
While significant associations have been reported between elevated glucose [4, 5], glycemic load , T2DM [2, 7], and a number of cancers, there is little information to support the influence of preexisting hyperglycemia on EOC . However, much of the literature relating cancer and glucose abnormalities comes from clinical or epidemiological studies that were not originally designed to evaluate the effects of hyperglycemia on cancer development . This is a particular limitation when looking at EOC because of its relatively low population incidence. In addition, many of the studies used diabetic status or a single glucose measurement as a proxy for classifying glucose abnormalities, likely underestimating the true hyperglycemic population. The changing profile of insulin status over the course of T2DM  probably further obscured any associations and there was poor consideration of confounding variables such as insulin, obesity, medication, and time since diagnosis.
The design of these population studies presumed that hyperglycemia was a direct and sufficient cause of ovarian cancer, when it may in fact be more important in the growth promotion of previously transformed cells. In this way, end-point analyses such as case-control or retrospective cohort studies would not be expected to show any association. A more useful consideration may be that of time to tumour development in patients with hyperglycemia. For example, in women already diagnosed with ovarian cancer, high glucose appears to be a poor prognostic factor . A further complication of these studies is that both hyperglycemia and EOC are notoriously quiet diseases in their early stages. This makes it very difficult from a population health standpoint to infer an association, or suggest causality, as the underlying pathologies of both diseases begin and may interact well before diagnosis.
Although population-based studies have not been supportive for a role of preexisting hyperglycemia in the development of ovarian cancer, recent basic science still suggests that EOC may be subject to the influence of high blood sugar. The rate of glucose uptake, which increases with increasing extracellular glucose , has been linked with tumour aggressiveness . EOC cells are also sensitive to complete glucose deprivation than nontransformed ovarian epithelial cells ; thus, they may also be very responsive to hyperglycemia.
3. Hyperinsulinemia versus Hyperglycemia
The impact of hyperinsulinemia on cancer has received much more research attention than the impact of hyperglycemia, although the two conditions are very closely related. It is well established that insulin promotes tumour growth. Insulin is mitogenic via its signaling through the insulin receptor and the insulin-like growth factor (IGF) pathways and direct anabolic signaling which is mediated by changes in the insulin receptor (IR) population. Expression of the IR is elevated in EOC, suggesting a tumour-promoting role in this cancer .
However, we contend that the specific impact of hyperglycemia on EOC is also an important area of research as abnormalities in glucose metabolism typically underlie hyperinsulinemia. Elevated insulin levels arise as a result of persistent hyperglycemia and peripheral insulin resistance. Thus, although insulin has direct, isolated actions on tumour growth, changes in glucose metabolism predispose changes in insulin signaling. In addition, it is becoming clear that there are insulin-independent mechanisms of glucose action on cancer risk, particularly through energy-sensing pathways and glucotoxic damage.
4.1. Historical Perspective on Hyperglycemia and Cancer
Almost 80 years ago, Dr. Warburg observed that, compared to normal cells, cancer cells show a preference for glycolysis and lactate production over oxidative phosphorylation . Because glycolysis is 18 times less efficient at producing ATP, this glycolytic switch suggests that cancer cells have an inherently high need for glucose. Furthermore, tumours are very active metabolically and require copious amounts of cellular fuel to meet growth demands. Aerobic glycolysis has been successfully exploited in EOC diagnostics in which tumour visualization occurs through the detection of the differential uptake of glucose in cancer cells compared to normal cells . The use of FdG-PET (18-fluoro-2-deoxyglucose positron emission tomography) demonstrates the association between tumour growth and energy availability.
Glucose metabolism of tumours was studied extensively starting in the 1950s. Warburg’s initial observation was bolstered by evidence that tumours could induce host hypoglycemia in a tumour mass-dependent fashion [18, 19]. In many tumour-bearing animals, there appeared to be host compensation for hypoglycemia at the level of the liver, with increased gluconeogenesis and glycogen mobilization . Local hypoglycemia in the area around the tumour was particularly pronounced [18, 20]. It was found that while tumours had the capacity to take up larger volumes of glucose in mildly hyperglycemic environments they were poor at compensating for low blood glucose by increasing glucose uptake [18, 20]. An important role for the vasculature was identified in hyperglycemic conditions, as tumours were able to increase glucose uptake by increasing glucose transfer across the capillary walls .
Following these metabolic observations, a number of groups looked at the growth characteristics of tumours in hyperglycemic environments. It was reported widely that profound hypoinsulinemia usually caused by chemical destruction of pancreatic -cells consistently caused a decrease in tumour growth [19, 21, 22]. The hypoinsulinemia was generally associated with significant hyperglycemia. However, in diabetic animals, combined treatment of both antitumour and antihyperglycemia therapies gave the best tumour-reductive outcome .
Although they demonstrated a negative effect of hyperglycemia on tumour development, these early studies have a number of limitations. The large transplantable tumours used were sustainable in vivo only for several weeks. The alloxan used to induce diabetes was toxic and administered systemically, and so may have had effects outside the target endocrine cells within the pancreas. Also, the studies that showed a decrease in tumour mass in the diabetic animals did not report the changes with respect to total animal mass, which is generally smaller in the diabetic animals.
The studies also seem to make the assumption that all glucose taken up is immediately metabolized. However, it was noted independently by several groups that glucose uptake was too high to be fully explained by the amount of tumour growth [20, 23]. These results suggest the possibility that cancer cells may be able to store fuel in times of high abundance. Nigam et al. concluded that low glycogen was due to defective glycogen synthesis and reported low activities of key glyconeogenic enzymes phosphoglucomutase and glycogen synthetase as compared to normal tissues . The low tumour glycogen was also linked to abnormally high rates of glycogen breakdown by phosphorylase. A recent article looking at glycogen levels in human colorectal cancer, however, reported that tumour cells actually had higher glycogen content than normal tissue . The authors noted that there was less glycogen in poorly differentiated tumours compared to well-differentiated tumours, suggesting that low glycogen may be an indicator of a poor prognosis. They also found a very clear negative correlation between glycogen level and proliferation index . The little research in this area has been carried out in normoglycemic conditions. It seems likely that, given the high rate of fuel usage in a tumour, at normoglycemic levels, there would be little need for storage as most would be used immediately. This brings up an intriguing question: could hyperfueled conditions favour a storage phenotype in cancer cells? This might explain the low growth rates of tumours in type one diabetic conditions.
Glycogen synthase kinase 3 (GSK3) phosphorylates and inactivates glycogen synthase, preventing the formation of glycogen. High levels of GSK3 have been implicated in the progression of a number of cancers, including ovarian cancer . GSK3 affects tumour growth through many different mechanisms, including NF-κB and Wnt signaling activation . Although it was not discussed in the literature reviewed here, GSK overexpression may be linked with glycogen storage and proliferation index. In summary, despite a number of investigations, carbohydrate metabolism by tumours is still poorly understood.
4.2. Hyperglycemia in EOC
We consider the possible effects of glucose on EOC development to be either “permissive” or “contributing”. Permissive effects are those that alter the energy status of cells, allowing tumour cells greater access to fuel. Contributing effects are those that directly damage protein or DNA in some cancer-promoting way.
Persistent elevations in blood sugar occur once hypersecretion of insulin is no longer able to compensate for combined insulin resistance and high glucose levels. The failure of insulin to facilitate glucose entry into cells is evaluated on a continuum, meaning that patients may have significant pathological changes while being in a “prediabetic” state. In fact, by time of diagnosis of T2DM, hyperglycemia has already caused vascular complications in at least 20% of patients [3, 27]. However, poor glycemic control is not solely due to impaired insulin signaling, as glucose has the ability to regulate its own clearance by mass action . Glucose self-regulation is impaired in people with hyperglycemia, leading to a state of glucose resistance . Chronic hyperglycemia downregulates enzymes responsible for glucose metabolism, including those of the energy-sensing AMP-activated protein kinase (AMPK) pathway . This results in fewer glucose transporters translocating to the cell surface, further impeding the cell’s ability to take up fuel. Gluconeogenesis also appears to be increased in patients with already elevated blood sugar . Thus, the effects of glucose join insulin resistance in maintaining and exacerbating hyperglycemia.
4.3. Permissive Effects of High Glucose: Energy Excess
It is postulated that where there is energy available tumour cells will have a suitable soil to grow. The biological plausibility of this excess energy hypothesis has been supported by a number of in vitro studies: Yamamoto et al. found that increasing glucose concentration in the culture media of MCF-7 breast cancer cells increased proliferation , mediated by an upregulation of cdk2 and cyclin D1 . In a line of choriocarcinoma cells, sustained hyperglycemia was found to stimulate the cell’s glucose transport system, increasing glucose uptake rates . In contrast, most nontransformed cells downregulate glucose transport in the presence of hyperglycemia. Studies in human breast cancer xenografts also suggest that the amount of glucose metabolism is not determined by metabolic demand, but rather by substrate availability . Conversely, energy restriction is protective in several cancer models . Together, these findings support the idea that the fuel availability in hyperglycemia may be permissive for cancer growth.
In hyperglycemia-induced insulin resistance, the ability of normal cells to access fuel is impaired. The correlation between cancer risk and T2DM suggests that where normal cells fail metabolically cancer cells excel. Mechanistically, this may involve the overexpression of components of the AMPK pathway . It is possible that in hyperglycemia cancer cells are inherently better at responding to the effects of insulin compared to insulin-resistant “normal” cells. In their 2004 paper, Gatenby and Gillies argue that mutations affecting substrate use cannot be early events in carcinogenesis because they would offer no advantage when there are no constraints on fuel availability, which typically arise in a larger tumour mass . While this is true in a normal cellular environment, in hyperglycemia there is a limit on substrate availability because of insulin resistance. Better access to the abundance of extracellular glucose, therefore, confers a selective growth advantage and could be an early marker of tumourigenic potential.
If conditions such as dysglycemia and diabetes prove to be involved in EOC initiation as well as promotion, then we propose that the selective pressures of the energy status may be an early event in the formation of EOC tumours. Cells that are best able to survive high glycemic conditions necessarily have a key characteristic of cancer cells, essentially obtaining self-sufficiency in growth signals . Thus, cancers that arise in a hyperglycemic environment may represent an unregulated adaptive survival response. Although there is currently no directly supportive data for this hypothesis, possible mechanisms for this relationship are described in the following sections.
4.4. Contributing Effects of High Glucose: Cellular and Genetic Damage
The consequences of chronic exposure to high glucose tend to be detrimental to cellular function and affect the physiology of the normal ovary . In fact, most long-term diabetic complications (retinopathy, neuropathy, and nephropathy) are consequences of hyperglycemia and cannot be reversed despite glucose normalization . However, this damage might also provide a mutational advantage to some cells by altering cellular proteins or DNA. Cancer development is often thought of in terms of a series of “hits”. The conditions of the tumour microenvironment, many of them determined by an altered metabolic profile, have been shown to contribute to the genetic instability of cancer cells , providing the necessary “hits” for a more aggressive tumour. Acidity, hypoxia, and formation of reactive oxygen species may all be enhanced in tumours in a hyperglycemic environment.
4.4.1. Acidic Environment
In tumour cells, high glucose flux through the glycolytic pathway produces large quantities of lactate, resulting in tumour tissue with pH 0.5 units lower than normal tissue . Cancerous cells adapt to this acidification, exhibiting maximal growth at the relatively low pH of about 6.8 . Tumours also have a capacity, similar to working skeletal muscle, to share lactate between hypoxic and nonhypoxic cells, so it is not extruded as a waste product . Despite these survival adaptations, tumour acidity has been shown to impair DNA repair mechanisms  and to upregulate angiogenic molecules such as vascular endothelial growth factor (VEGF) and IL-8 in order to enhance lactate clearance [43, 44]. Experimental evidence demonstrates that the acidic environment is supportive of tumourigenesis, increasing resistance to chemotherapy , mutation rate , and invasion capability . The acid-mediated tumour invasion hypothesis postulates that H+ ions from the tumour microenvironment diffuse down their concentration gradient into the surrounding normal tissue . Because the normal cells cannot survive the increase in acidity, the border of malignant tissue is progressively pushed forward. In fact, mathematical modeling has shown that tumour acid production alone can explain patterns of tumour growth . The effects of acidity are particularly important in a hyperglycemic environment because increased glucose flux through tumour cells has been shown to create a large increase in lactate production [33, 49].
4.4.2. Transient Hypoxia
The characteristic microvascular damage caused by hyperglycemia  may lead to periods of hypoxia, possibly through a nitric-oxide-mediated mechanism. The bioavailability of the vasodilator is decreased in diabetes  as it is scavenged by superoxide radicals to form the highly reactive molecule . Transient hypoxia is thought to be one of the strongest pressures for cells to undergo transformation and is a central hypothesis explaining the glycolytic switch [13, 53]. Hypoxic conditions also increase the activity of hypoxia-inducible factor (HIF-1) and VEGF, which are strongly associated with both tumour angiogenesis and EOC tumour aggressiveness [54, 55].
4.4.3. Oxidative Stress
Levels of oxidative stress reflect the ability to balance production and elimination of highly reactive free radicals, which include the family of reactive oxygen species (ROS). Oxidative stress is known to be higher in diabetic patients than in healthy individuals , and it is often cited as a unifying theory to explain tissue damage by hyperglycemia . Because ROS can also create DNA damage through a number of mechanisms , it has similarly been proposed that carcinogenesis in general is caused by oxidative stress . This stress in ovarian epithelial cells specifically is thought to be a potential initiator of tumourigenesis . Hyperglycemia also causes increased flux of glucose through the aldose-reductase (polyol) pathway, which has been postulated to increase sensitivity to oxidative stress by reducing regeneration of the antioxidant glutathione . While epidemiological studies evaluating antioxidant use in diabetes [52, 61] and ovarian cancer  have not been conclusive, preliminary results suggest that this therapeutic avenue is worth further exploration. A recent study of flavonoids with antioxidant effects found that they inhibited cell growth and VEGF expression in ovarian cancer cells .
Much of the tissue damage and cellular dysfunction associated with hyperglycemia has been attributed to advanced glycation end products (AGEs) created by the nonenzymatic glycation of proteins . While AGE accumulation is a normal part of aging, it occurs at an accelerated rate in diabetes where progressive modifications can lead to irreversible cross-linking, impairing the actions of other molecules [64, 65]. Receptors for AGE (RAGE) mediate many more severe actions and potentiate the cellular response . RAGEs are upregulated by presence of AGE ligands, and AGE-RAGE binding protects the ligands, allowing them to persist in the environment . AGE-RAGE interaction has been shown to stimulate tumour cell growth or invasiveness in pancreatic cancer , melanoma , and glioma , while blocking the RAGE inhibits tumour formation and metastasis [68, 69]. The ovarian surface epithelium may be particularly susceptible to the effects of glycation damage because not only the tissue is well vascularized, but it is also in constant contact with peritoneal fluid, whose glucose content is reflective of blood glucose levels .
Mechanistically, AGE-RAGE signaling has been linked to induction of an inflammatory response in the vasculature , as well as an increase in matrix metalloproteinases (MMPs)-2 and -9 , and may, therefore, play a role in determining tumour invasiveness. Because AGE-RAGE signaling seems to be part of the chronic rather than acute response , its contributions to the development of tumour formation are quite plausible.
Glucose reactivity in hyperglycemia can also lead to glucose autoxidation, generating hydroxide radicals, and contributing to the burden of oxidative stress . Also, apart from RAGE signaling, glucose moieties on proteins can donate electrons to form hydrogen peroxide, directly activating NF-κB [73, 74] and contributing to an inflammatory response. There is evidence that changes to local tissue can enhance the possibility of tumour spread , possibly implicating glucose-induced damage to the peritoneal cavity as a permissive factor for ovarian tumour metastasis .
4.5. The Role of Glucose Transporters
Glucose is a large, hydrophilic molecule that cannot diffuse through the lipid bilayer of cells on its own, and thus requires specific transporter proteins. Glucose enters cells by facilitated diffusion mainly through glucose transporters (GLUTs), and the activation of GLUT genes is one of the earliest events in oncogenesis . Because GLUTs have a role in glucose sensing and respond to extracellular glucose concentrations, these transporters may be very important in a hyperglycemic environment. GLUT1 in particular is highly expressed in ovarian cancer , where tumour status (benign, borderline, or malignant) is correlated with the level of GLUT1 expression . Almost all invasive epithelial carcinomas are positive for GLUT1, independent of stage, grade, or histological subtype [79, 80]. Antibodies to GLUT1 decrease proliferation, induce apoptosis in nonsmall cell lung cancer and breast cancer cell lines, and appear to synergize with a number of chemotherapeutics to enhance their apoptotic effects .
Very recently, another class of transporters, sodium/glucose cotransporters (SGLTs), was shown to be associated with the epidermal growth factor receptor (EGFR) in cancer cells . The authors of the study proposed that SGLTs may enhance tumourigenesis by making cells independent of the glucose concentration gradient, allowing them to take up fuel in any situation. This hypothesis is in line with the proposal made here that permissive effects of glucose are cancer causing: removing restrictions on fuel availability seems to enhance tumourigenesis. The EGFR is particularly important in ovarian cancer; it is normally expressed on ovarian surface epithelium and is often overexpressed in EOC. The expression of key glucose transporters in ovarian cancer is summarized in Table 1.
5. Inflammation and EOC
In both rats and humans, hyperglycemia has been shown to be a major cause of the systemic inflammatory response [99, 100]. Both oxidative stress  and AGE-RAGE  signaling are also implicated in promoting systemic inflammation in hyperglycemic environments.
Inflammation is thought to be associated with cancer development mechanistically because of rapid cell division, DNA excision and repair, oxidative stress, and high concentrations of cytokines and prostaglandins; all of which are promoters of mutagenesis . Moreover, inflammation has been proposed as a unifying hypothesis for the development of EOC . The high concentrations of circulating growth-promoting and inflammatory cytokines as a result of hyperglycemia may mean that factors, which normally in an autocrine or paracrine fashion  are instead coming from the systemic environment and exerting an endocrine effect, potentiate tumour growth. In support of this, animal knockout studies have shown that MMP production by the host may be more important in carcinogenesis than MMP production by tumour cells themselves .
Cytokines can affect EOC tumour growth by acting as growth factors, increasing angiogenesis, or an immunomodulatory pathway whereby they prevent cellular recognition and destruction of the tumour. A number of cytokines that are increased as part of systemic inflammation in diabetes also have tumour promoting effects in ovarian cancer . IL-1 and TNF- are thought to increase production of IL-6, which promotes cell attachment and migration  and also blocks apoptosis induced by cytotoxic agents . IL-8 and TGF- promote tumour angiogenesis . In addition, although TGF- normally inhibits epithelial cell proliferation , repeated exposure to high levels may attenuate the response of cancerous epithelial cells .
The inflammatory hypothesis lends itself to testing with a variety of antiinflammatory drugs and indeed early studies show promise. A study evaluating human ovarian tumours in nude mice concluded that cyclooxygenase inhibitors limited tumour growth, in part through an antiangiogenic mechanism . Epidemiologically, patients with chronic aspirin, NSAID, or acetaminophen use have been shown to have a reduced risk of EOC . However, as with antioxidant trials, these observational studies are still preliminary .
5.1. The Incessant Ovulation Hypothesis
Recently, the inflammation associated with postovulatory follicle repair has received attention as a possible contributor to EOC promotion . The incessant ovulation hypothesis purports that the repeated damage and repair cycles associated with ovulation enhance the possibility for mutagenesis. Incessant ovulation also increases the likelihood that inclusion cysts will form, trapping epithelial cells in the hormone-rich environment of the ovarian stroma [1, 111]. If these trapped cells are inappropriately maintained, they are more likely to transform [111–113]. Wound healing in hyperglycemia is characteristically slow and almost certainly influenced by the effects of inflammation and damage from glycation. Lowered nitric oxide bioavailability in combination with the tissue damage caused by hyperglycemia may be partly responsible . In one study AGE-RAGE blockade decreased expression of inflammatory cytokines and MMPs resulting in normalization of wound closure in a genetic mouse model of diabetes . Taken together, the mutagenic risk and the risk of entrapment in inclusion cysts from repeated ovulations, combined with impaired wound healing, might mean a greater risk for ovarian cancer development in a hyperglycemic environment. This idea provides a possible mechanism by which hyperglycemia may initiate cancer, in addition to playing a role in promotion of EOC from an unrelated transforming event.
6. Glucose, Angiogenesis, and Tumour Formation
As hypothesized by Dr. Folkman , solid tumours must recruit new blood vessels in order to grow beyond 1-2 mm in size. Most of the tumour vascularization occurs through angiogenesis, which is the development of new blood vessels from preexisting vasculature. The angiogenic process is regulated by a balance between pro- and anti-angiogenic factors and in ovarian cancer there is a concomitant overexpression of proangiogenic factors and an inhibition of anti-angiogenic molecules . There are numerous reports concluding that elevated glucose levels contribute to increased angiogenic processes. Granulosa cell tumours of the ovary have been shown to have increased expression of members of both the glycolytic and angiogenic pathways . Glucose directly increases expression of the potent proangiogenic factor VEGF, which is thought to be the mechanism involved in the vascular complications associated with diabetes (reviewed in ). In a similar fashion to tumour cells, endothelial cells that comprise the tumour vasculature also increase their utilization of glucose. Glucose transporter expression is increased in the hypoxic environment associated with most solid tumours , and glucose increases survival of both tumour epithelial and endothelial cells . Because increased tumour vascularity is correlated with increased metastatic potential and tumour progression [121, 122], the proangiogenic inflammatory environment of hyperglycemia may also promote carcinogenesis. Unfortunately, inflammation may be self-promoting as increased tumour perfusion can act to further exacerbate the immune response .
In addition to the direct effects of glucose, the effects of inflammation are likely mediated by VEGF. Inflammatory mediators upregulate VEGF and VEGF receptors, which are correlated with the clinical outcomes of ovarian cancer patients . For example, NF-κB can promote angiogenesis by activating VEGF and IL-8  and may be central to inflammation-induced tumour growth and progression . MMPs can also stimulate proliferation and release of VEGF .
The possible impact of hyperglycemia-related inflammation on cancer suggests that anti-angiogenic molecules such as thrombospondin-1 may be of great benefit in treating diabetic tumours . The relationship between angiogenesis, inflammation, and carcinogenesis is illustrated by the fact that a number of anti-angiogenic drugs that are promising in the treatment of cancer are also effective against chronic inflammatory diseases .
7. Antidiabetic Drugs as Targeted EOC Therapy
Because of the multitude of protumour effects of glucose, it is intuitive that glucose deprivation may be a potent antitumour treatment approach. From the literature, it is apparent that glucose is an important energy substrate, survival factor, and proangiogenic molecule. There are a number of antihyperglycemic treatments currently available for reducing serum blood glucose and these drugs may effectively inhibit glucose availability to the tumour. Although the effects of antihyperglycemic drugs are well documented in diabetes, their effects in cancer are relatively unknown. Preliminary reports show that these drugs may have multi-modal effects in slowing tumour growth. In an approach similar to that using anti-angiogenic drugs, the class of antihyperglycemic drugs such as metformin and rosiglitazone may reduce glucose availability to the tumour and essentially starve the tumour of nutrients. These drugs have also been shown to have direct effects on metabolic and signaling pathways that may be independent of glucose.
Metformin is in the biguanide class of antidiabetic drugs and decreases circulating glucose levels by suppressing hepatic production of glucose . Metformin, by reducing insulin and glucose levels, reduced the size and increased latency of mammary adenocarcinomas in HER-2/neu transgenic mice, demonstrating a potent antitumour effect . In vitro, metformin significantly inhibits the growth of epithelial ovarian cancer cells and may potentiate the effects of the common chemotherapy drug cisplatin . Metformin may preferentially increase peripheral glucose uptake in skeletal muscle, as administration increases AMPK activity in skeletal muscle  and stimulates translocation of muscle GLUT-4 . This favoured packaging of glucose into skeletal muscle cells would decrease serum glucose levels and availability to the tumour cells resulting in nutrient depletion. Stimulation of AMPK by metformin also contributes to the reduced hepatocyte production of glucose . In fact, AMPK activation is associated with an inhibition of tumourigenesis through apoptosis induction, decreased cell proliferation and may be a communal molecule utilized by metformin as well as a number of anti-tumour drugs that have been shown to have effects in EOC. C93 , resveratrol [13, 136], 2-deoxy-D-glucose , and AICAR  are targeted therapies that are effective in the treatment of ovarian cancer. Interestingly, these molecules also cause the stimulation of AMPK, indicating a common pathway intersection with metformin. Although not yet investigated, there is a possibility that metformin may have a synergistic interaction with these molecules, in addition to its glucose deprivation effects.
Rosiglitazone is another antidiabetic agent in the thiazolidinedione class of drugs designed to reduce the hyperglycemia associated with this disease. Rosiglitazone activates the peroxisome proliferator activated receptors (PPAR) in target tissues, increasing insulin sensitivity and decreasing serum levels of glucose. As with metformin, rosiglitazone also stimulates increased expression of GLUT-4  causing glucose uptake in skeletal muscle . One of the mechanisms by which rosiglitazone may have a significant antitumour effect is through the inhibition of angiogenesis. Rosiglitazone has been shown to inhibit VEGF-induced angiogenesis  and is suggested as a treatment option for vascular disorders associated with diabetes such as diabetic retinopathy, macular degeneration, and so forth. As VEGF expression is significantly elevated in EOC  and is responsible for some of the ovarian tumour vascularization (reviewed in ), rosiglitazone may have a bimodal anti-tumour effect by decreasing glucose availability and also by reducing tumour angiogenesis. Simply by decreasing tumour vascularity, rosiglitazone will decrease glucose delivery to the tumour by decreasing tumour tissue perfusion.
8. Summary and Conclusions
An emerging view of cancer relies on an initiation-promotion paradigm that suggests a fundamental role of the tumour environment on cancer development. New data suggests that hyperglycemia may be a contributing factor to the onset and progression of EOC through a number of complex mechanisms (summarized in Figure 1). We propose that hyperglycemia has important effects on both the progression and somatic evolution of epithelial ovarian cancer. Altered glucose homeostasis is common in cancer patients, so antihyperglycemic therapies are applicable to even those who have normal blood sugar. Although there are a number of cellular mechanisms through which hyperglycemia may effect the promotion or initiation of ovarian cancer, there is almost no in vivo experimental data exploring the link between hyperglycemia and EOC. Further research in this area not only has applications in the development of cancer therapeutics, but also will provide new insights into EOC pathogenesis, early detection, and possible prevention.
- C. N. Landen Jr., M. J. Birrer, and A. K. Sood, “Early events in the pathogenesis of epithelial ovarian cancer,” Journal of Clinical Oncology, vol. 26, no. 6, pp. 995–1005, 2008.
- S. Cowey and R. W. Hardy, “The metabolic syndrome: a high-risk state for cancer?” American Journal of Pathology, vol. 169, no. 5, pp. 1505–1522, 2006.
- M. I. Harris, R. Klein, T. A. Welborn, and M. W. Knuiman, “Onset of NIDDM occurs at least 4–7 yr before clinical diagnosis,” Diabetes Care, vol. 15, no. 7, pp. 815–819, 1992.
- S. H. Jee, H. Ohrr, J. W. Sull, J. E. Yun, M. Ji, and J. M. Samet, “Fasting serum glucose level and cancer risk in Korean men and women,” Journal of the American Medical Association, vol. 293, no. 2, pp. 194–202, 2005.
- K.-T. Khaw, N. Wareham, S. Bingham, R. Luben, A. Welch, and N. Day, “Preliminary communication: glycated hemoglobin, diabetes, and incident colorectal cancer in men and women: a prospective analysis from the European Prospective Investigation into Cancer-Norfolk Study,” Cancer Epidemiology Biomarkers and Prevention, vol. 13, no. 6, pp. 915–919, 2004.
- H. G. Mulholland, L. J. Murray, C. R. Cardwell, and M. M. Cantwell, “Dietary glycaemic index, glycaemic load and endometrial and ovarian cancer risk: a systematic review and meta-analysis,” British Journal of Cancer, vol. 99, no. 3, pp. 434–441, 2008.
- S. S. Coughlin, E. E. Calle, L. R. Teras, J. Petrelli, and M. J. Thun, “Diabetes mellitus as a predictor of cancer mortality in a large cohort of US adults,” American Journal of Epidemiology, vol. 159, no. 12, pp. 1160–1167, 2004.
- L. A. Brinton, L. C. Sakoda, K. Frederiksen, et al., “Relationships of uterine and ovarian tumors to pre-existing chronic conditions,” Gynecologic Oncology, vol. 107, no. 3, pp. 487–494, 2007.
- E. Giovannucci, “The role of insulin resistance and hyperinsulinemia in cancer causation,” Current Medicinal Chemistry, vol. 5, no. 1, pp. 53–60, 2005.
- F. B. Hu, J. E. Manson, S. Liu, et al., “Prospective study of adult onset diabetes mellitus (type 2) and risk of colorectal cancer in women,” Journal of the National Cancer Institute, vol. 91, no. 6, pp. 542–547, 1999.
- D. M. Lamkin, D. R. Spitz, M. M. K. Shahzad, et al., “Glucose as a prognostic factor in ovarian carcinoma,” Cancer, vol. 115, no. 5, pp. 1021–1027, 2009.
- C. Bouché, S. Serdy, C. R. Kahn, and A. B. Goldfine, “The cellular fate of glucose and its relevance in type 2 diabetes,” Endocrine Reviews, vol. 25, no. 5, pp. 807–830, 2004.
- R. A. Gatenby and R. J. Gillies, “Why do cancers have high aerobic glycolysis?” Nature Reviews Cancer, vol. 4, no. 11, pp. 891–899, 2004.
- A. Kueck, A. W. Opipari Jr., K. A. Griffith, et al., “Resveratrol inhibits glucose metabolism in human ovarian cancer cells,” Gynecologic Oncology, vol. 107, no. 3, pp. 450–457, 2007.
- K. R. Kalli, O. I. Falowo, L. K. Bale, M. A. Zschunke, P. C. Roche, and C. A. Conover, “Functional insulin receptors on human epithelial ovarian carcinoma cells: implications for IGF-II mitogenic signaling,” Endocrinology, vol. 143, no. 9, pp. 3259–3267, 2002.
- O. Warburg, The Metabolism of Tumours, Constable Press, London, UK, 1930.
- A. M. Lutz, P. Ray, J. K. Willmann, C. Drescher, and S. S. Gambhir, “2-deoxy-2-[F-18]fluoro-D-glucose accumulation in ovarian carcinoma cell lines,” Molecular Imaging and Biology, vol. 9, no. 5, pp. 260–266, 2007.
- V. S. Shapot and V. A. Blinov, “Blood glucose levels and gluconeogenesis in animals bearing transplantable tumors,” Cancer Research, vol. 34, no. 8, pp. 1827–1832, 1974.
- K. Pavelic, M. Slijepcevic, J. Pavelic, et al., “Growth and treatment of Ehrlich tumor in mice with alloxan-induced diabetes,” Cancer Research, vol. 39, no. 5, pp. 1807–1813, 1979.
- P. M. Gullino, F. H. Grantham, and A. H. Courtney, “Glucose consumption by transplanted tumors in vivo,” Cancer Research, vol. 27, no. 6, pp. 1031–1040, 1967.
- E. S. Goranson and G. J. Tilser, “Studies on the relationship of alloxan-diabetes and tumor growth,” Cancer Research, vol. 15, pp. 626–631, 1955.
- C. L. Puckett and W. W. Shingleton, “The effect of induced diabetes on experimental tumor growth in mice,” Cancer Research, vol. 32, no. 4, pp. 789–790, 1972.
- P. M. Gullino, F. H. Grantham, A. H. Courtney, and I. Losonczy, “Relationship between oxygen and glucose consumption by transplanted tumors in vivo,” Cancer Research, vol. 27, no. 6, pp. 1041–1052, 1967.
- V. N. Nigam, H. L. MacDonald, and A. Cantero, “Limiting factors for glycogen storage in tumors, I. Limiting enzymes,” Cancer Research, vol. 22, pp. 131–138, 1962.
- S. Takahashi, A. Satomi, K. Yano, et al., “Estimation of glycogen levels in human colorectal cancer tissue: relationship with cell cycle and tumor outgrowth,” Journal of Gastroenterology, vol. 34, pp. 474–480, 1999.
- Q. Cao, X. Lu, and Y.-J. Feng, “Glycogen synthase kinase-3 positively regulates the proliferation of human ovarian cancer cells,” Cell Research, vol. 16, no. 7, pp. 671–677, 2006.
- M. J. Legato, A. Gelzer, R. Goland, et al., “Gender-specific care of the patient with diabetes: review and recommendations,” Gender Medicine, vol. 3, no. 2, pp. 131–158, 2006.
- S. I. Itani, A. K. Saha, T. G. Kurowski, H. R. Coffin, K. Tornheim, and N. B. Ruderman, “Glucose autoregulates its uptake in skeletal muscle: involvement of AMP-activated protein kinase,” Diabetes, vol. 52, no. 7, pp. 1635–1640, 2003.
- M. J. Birnbaum, “Signal transduction: sweet conundrum,” Science, vol. 319, no. 5868, pp. 1348–1349, 2008.
- M. Yamamoto, N. A. Patel, J. Taggart, R. Sridhar, and D. R. Cooper, “A shift from normal to high glucose levels stimulates cell proliferation in drug sensitive MCF-7 human breast cancer cells but not in multidrug resistant MCF-7/ADR cells which overproduce PKC-II,” International Journal of Cancer, vol. 83, no. 1, pp. 98–106, 1999.
- M. Okumura, M. Yamamoto, H. Sakuma, et al., “Leptin and high glucose stimulate cell proliferation in MCF-7 human breast cancer cells: reciprocal involvement of PKC- and PPAR expression,” Biochimica et Biophysica Acta, vol. 1592, no. 2, pp. 107–116, 2002.
- T. Hahn, S. Barth, W. Hofmann, O. Reich, I. Lang, and G. Desoye, “Hyperglycemia regulates the glucose-transport system of clonal choriocarcinoma cells in vitro. A potential molecular mechanism contributing to the adjunct effect of glucose in tumor therapy,” International Journal of Cancer, vol. 78, no. 3, pp. 353–360, 1998.
- F. Kallinowski, P. Vaupel, S. Runkel, et al., “Glucose uptake, lactate release, ketone body turnover, metabolic micromilieu, and pH distributions in human breast cancer xenografts in nude rats,” Cancer Research, vol. 48, no. 24, pp. 7264–7272, 1988.
- S. D. Hursting, J. A. Lavigne, D. Berrigan, S. N. Perkins, and J. C. Barrett, “Calorie restriction, aging, and cancer prevention: mechanisms of action and applicability to humans,” Annual Review of Medicine, vol. 54, pp. 131–152, 2003.
- H. Ashrafian, “Cancer's sweet tooth: the Janus effect of glucose metabolism in tumorigenesis,” The Lancet, vol. 367, no. 9510, pp. 618–621, 2006.
- D. Hanahan and R. A. Weinberg, “The hallmarks of cancer,” Cell, vol. 100, no. 1, pp. 57–70, 2000.
- M. Doblado and K. H. Moley, “Glucose metabolism in pregnancy and embryogenesis,” Current Opinion in Endocrinology, Diabetes and Obesity, vol. 14, no. 6, pp. 488–493, 2007.
- A. P. Rolo and C. M. Palmeira, “Diabetes and mitochondrial function: role of hyperglycemia and oxidative stress,” Toxicology and Applied Pharmacology, vol. 212, no. 2, pp. 167–178, 2006.
- J. Yuan, L. Narayanan, S. Rockwell, and P. M. Glazer, “Diminished DNA repair and elevated mutagenesis in mammalian cells exposed to hypoxia and low pH,” Cancer Research, vol. 60, no. 16, pp. 4372–4376, 2000.
- K. Smallbone, D. J. Gavaghan, R. A. Gatenby, and P. K. Maini, “The role of acidity in solid tumour growth and invasion,” Journal of Theoretical Biology, vol. 235, no. 4, pp. 476–484, 2005.
- J. J. Casciari, S. V. Sotirchos, and R. M. Sutherland, “Variations in tumor cell growth rates and metabolism with oxygen concentration, glucose concentration, and extracellular pH,” Journal of Cellular Physiology, vol. 151, no. 2, pp. 386–394, 1992.
- P. Sonveaux, F. Végran, T. Schroeder, et al., “Targeting lactate-fueled respiration selectively kills hypoxic tumor cells in mice,” Journal of Clinical Investigation, vol. 118, no. 12, pp. 3930–3942, 2008.
- Q. Shi, J. L. Abbruzzese, S. Huang, I. J. Fidler, Q. Xiong, and K. Xie, “Constitutive and inducible interleukin 8 expression by hypoxia and acidosis renders human pancreatic cancer cells more tumorigenic and metastatic,” Clinical Cancer Research, vol. 5, no. 11, pp. 3711–3721, 1999.
- L. Xu, D. Fukumura, and R. K. Jain, “Acidic extracellular pH induces vascular endothelial growth factor (VEGF) in human glioblastoma cells via ERK1/2 MAPK signaling pathway. Mechanism of low pH-induced VEGF,” Journal of Biological Chemistry, vol. 277, no. 13, pp. 11368–11374, 2002.
- N. Raghunand, B. Mahoney, R. van Sluis, B. Baggett, and R. J. Gillies, “Acute metabolic alkalosis enhances response of C3h mouse mammary tumors to the weak base mitoxantrone,” Neoplasia, vol. 3, no. 3, pp. 227–235, 2001.
- T. Morita, T. Nagaki, I. Fukuda, and K. Okumura, “Clastogenicity of low pH to various cultured mammalian cells,” Mutation Research, vol. 268, no. 2, pp. 297–305, 1992.
- R. Martinez-Zaguilan, E. A. Seftor, R. E. B. Seftor, Y.-W. Chu, R. J. Gillies, and M. J. C. Hendrix, “Acidic pH enhances the invasive behavior of human melanoma cells,” Clinical and Experimental Metastasis, vol. 14, no. 2, pp. 176–186, 1996.
- R. A. Gatenby and E. T. Gawlinski, “A reaction-diffusion model of cancer invasion,” Cancer Research, vol. 56, no. 24, pp. 5745–5753, 1996.
- D. E. Scheim and J. Y. Lin, “Glucose effects in an ovarian cancer protocol of exceptional activity,” Medical Hypotheses, vol. 40, no. 4, pp. 235–244, 1993.
- M. J. Sheetz and G. L. King, “Molecular understanding of hyperglycemia's adverse effects for diabetic complications,” Journal of the American Medical Association, vol. 288, no. 20, pp. 2579–2588, 2002.
- A. Riad, D. Westermann, S. V. Linthout, et al., “Enhancement of endothelial nitric oxide synthase production reverses vascular dysfunction and inflammation in the hindlimbs of a rat model of diabetes,” Diabetologia, vol. 51, no. 12, pp. 2325–2332, 2008.
- J. S. Johansen, A. K. Harris, D. J. Rychly, and A. Ergul, “Oxidative stress and the use of antioxidants in diabetes: linking basic science to clinical pratice,” Cardiovascular Diabetology, vol. 4, article 5, 2005.
- X. L. Zu and M. Guppy, “Cancer metabolism: facts, fantasy, and fiction,” Biochemical and Biophysical Research Communications, vol. 313, no. 3, pp. 459–465, 2004.
- A. Daponte, M. Ioannou, I. Mylonis, et al., “Prognostic significance of hypoxia-inducible factor 1 alpha(HIF-1alpha) expression in serous ovarian cancer: an immunohistochemical study,” BMC Cancer, vol. 8, article 335, 2008.
- E. M. Hartenbach, T. A. Olson, J. J. Goswitz, et al., “Vascular endothelial growth factor (VEGF) expression and survival in human epithelial ovarian carcinomas,” Cancer Letters, vol. 121, no. 2, pp. 169–175, 1997.
- S. H. Jee, H. J. Kim, and J. Lee, “Obesity, insulin resistance and cancer risk,” Yonsei Medical Journal, vol. 46, no. 4, pp. 449–455, 2005.
- J. M. Fernández-Real and J. C. Pickup, “Innate immunity, insulin resistance and type 2 diabetes,” Trends in Endocrinology and Metabolism, vol. 19, no. 1, pp. 10–16, 2008.
- M. Valko, M. Izakovic, M. Mazur, C. J. Rhodes, and J. Telser, “Role of oxygen radicals in DNA damage and cancer incidence,” Molecular and Cellular Biochemistry, vol. 266, no. 1-2, pp. 37–56, 2004.
- B. N. Ames, L. S. Gold, and W. C. Willett, “The causes and prevention of cancer,” Proceedings of the National Academy of Sciences of the United States of America, vol. 92, no. 12, pp. 5258–5265, 1995.
- W. J. Murdoch and J. F. Martinchick, “Oxidative damage to DNA of ovarian surface epithelial cells affected by ovulation: carcinogenic implication and chemoprevention,” Experimental Biology and Medicine, vol. 229, no. 6, pp. 546–552, 2004.
- J. L. Evans, “Antioxidants: do they have a role in the treatment of insulin resistance?” Indian Journal of Medical Research, vol. 125, no. 3, pp. 355–372, 2007.
- D. W. Cramer, H. Kuper, B. L. Harlow, and L. Titus-Ernstoff, “Carotenoids, antioxidants and ovarian cancer risk in pre- and postmenopausal women,” International Journal of Cancer, vol. 94, no. 1, pp. 128–134, 2001.
- H. Luo, B.-H. Jiang, S. M. King, and Y. C. Chen, “Inhibition of cell growth and VEGF expression in ovarian cancer cells by flavonoids,” Nutrition and Cancer, vol. 60, no. 6, pp. 800–809, 2008.
- S. Yamagishi, K. Nakamura, H. Inoue, S. Kikuchi, and M. Takeuchi, “Possible participation of advanced glycation end products in the pathogenesis of colorectal cancer in diabetic patients,” Medical Hypotheses, vol. 64, no. 6, pp. 1208–1210, 2005.
- M. Brownlee, “Advanced protein glycosylation in diabetes and aging,” Annual Review of Medicine, vol. 46, pp. 223–234, 1995.
- A. M. Schmidt, S. D. Yan, S. F. Yan, and D. M. Stern, “The multiligand receptor RAGE as a progression factor amplifying immune and inflammatory responses,” Journal of Clinical Investigation, vol. 108, no. 7, pp. 949–955, 2001.
- Y. Yamamoto, S.-I. Yamagishi, C.-C. Hsu, and H. Yamamoto, “Advanced glycation endproducts-receptor interactions stimulate the growth of human pancreatic cancer cells through the induction of platelet-derived growth factor-B,” Biochemical and Biophysical Research Communications, vol. 222, no. 3, pp. 700–705, 1996.
- R. Abe, T. Shimizu, H. Sugawara, et al., “Regulation of human melanoma growth and metastasis by AGE-AGE receptor interactions,” Journal of Investigative Dermatology, vol. 122, no. 2, pp. 461–467, 2004.
- A. Taguchi, D. C. Blood, G. del Toro, et al., “Blockade of RAGE-amphoterin signalling suppresses tumour growth and metastases,” Nature, vol. 405, no. 6784, pp. 354–360, 2000.
- G. Velho, Ph. Froguel, and G. Reach, “Determination of peritoneal glucose kinetics in rats: implications for the peritoneal implantation of closed-loop insulin delivery systems,” Diabetologia, vol. 32, no. 6, pp. 331–336, 1989.
- S. Yamagishi and M. Takeuchi, “Nifedipine inhibits gene expression of receptor for advanced glycation end products (RAGE) in endothelial cells by suppressing reactive oxygen species generation,” Drugs under Experimental and Clinical Research, vol. 30, no. 4, pp. 169–175, 2004.
- J. V. Hunt, R. T. Dean, and S. P. Wolff, “Hydroxyl radical production and autoxidative glycosylation. Glucose autoxidation as the cause of protein damage in the experimental glycation model of diabetes mellitus and ageing,” Biochemical Journal, vol. 256, no. 1, pp. 205–212, 1988.
- Y. Mizukami, W.-S. Jo, E.-M. Duerr, et al., “Induction of interleukin-8 preserves the angiogenic response in HIF-1 alpha-deficient colon cancer cells,” Nature Medicine, vol. 11, no. 9, pp. 992–997, 2005.
- T. Hellwig-Burgel, D. P. Stiehl, A. E. Wagner, E. Metzen, and W. Jelkmann, “Hypoxia-inducible factor-1 (HIF-1): a novel transcription factor in immune reactions,” Journal of Interferon and Cytokine Research, vol. 25, no. 6, pp. 297–310, 2005.
- E. Wang, Y. Ngalame, M. C. Panelli, et al., “Peritoneal and subperitoneal stroma may facilitate regional spread of ovarian cancer,” Clinical Cancer Research, vol. 11, no. 1, pp. 113–122, 2005.
- R. S. Freedman, M. Deavers, J. Liu, and E. Wang, “Peritoneal inflammation—a microenvironment for epithelial ovarian cancer (EOC),” Journal of Translational Medicine, vol. 2, article 23, 2004.
- K. Shibata, H. Kajiyama, Y. Mizokami, et al., “Placental leucine aminopeptidase (P-LAP) and glucose transporter 4 (Glut4) expression in benign, borderline, and malignant ovarian epithelia,” Gynecologic Oncology, vol. 98, no. 1, pp. 11–18, 2005.
- M. Tsukioka, Y. Matsumoto, M. Noriyuki, et al., “Expression of glucose transporters in epithelial ovarian carcinoma: correlation with clinical characteristics and tumor angiogenesis,” Oncology Reports, vol. 18, no. 2, pp. 361–367, 2007.
- C. Rudlowski, M. Moser, A. J. Becker, et al., “Glut1 mRNA and protein expression in ovarian borderline tumors and cancer,” Oncology, vol. 66, no. 5, pp. 404–410, 2004.
- T. Kalir, B. Y. Wang, M. Goldfischer, et al., “Immunohistochemical staining of Glut1 in benign, borderline, and malignant ovarian epithelia,” Cancer, vol. 94, no. 4, pp. 1078–1082, 2002.
- S. Rastogi, S. Banerjee, S. Chellappan, and G. R. Simon, “Glut-1 antibodies induce growth arrest and apoptosis in human cancer cell lines,” Cancer Letters, vol. 257, no. 2, pp. 244–251, 2007.
- R. S. Brown and R. L. Wahl, “Overexpression of Glut-1 glucose transporter in human breast cancer: an immunohistochemical study,” Cancer, vol. 72, no. 10, pp. 2979–2985, 1993.
- M. A. Stackhouse, D. J. Buchsbaum, S. R. Kancharla, et al., “Specific membrane receptor gene expression targeted with radiolabeled peptide employing the erbB-2 and DF3 promoter elements in adenoviral vectors,” Cancer Gene Therapy, vol. 6, no. 3, pp. 209–219, 1999.
- M. Kunkel, M. Moergel, M. Stockinger, et al., “Overexpression of Glut-1 is associated with resistance to radiotherapy and adverse prognosis in squamous cell carcinoma of the oral cavity,” Oral Oncology, vol. 43, no. 8, pp. 796–803, 2007.
- J. Gu, H. Yamamoto, H. Fukunaga, et al., “Correlation of Glut-1 overexpression, tumor size, and depth of invasion with 18F-2-fluoro-2-deoxy-D-glucose uptake by positron emission tomography in colorectal cancer,” Digestive Diseases and Sciences, vol. 51, no. 12, pp. 2198–2205, 2006.
- P. Effert, A. J. Beniers, Y. Tamimi, S. Handt, and G. Jakse, “Expression of glucose transporter 1 (Glut-1) in cell lines and clinical specimens from human prostate adenocarcinoma,” Anticancer Research, vol. 24, no. 5, pp. 3057–3063, 2004.
- H. Ito, M. Duxbury, M. J. Zinner, S. W. Ashley, and E. E. Whang, “Glucose transporter-1 gene expression is associated with pancreatic cancer invasiveness and MMP-2 activity,” Surgery, vol. 136, no. 3, pp. 548–556, 2004.
- L. E. Mendez, N. Manci, G. Cantuaria, et al., “Expression of glucose transporter-1 in cervical cancer and its precursors,” Gynecologic Oncology, vol. 86, no. 2, pp. 138–143, 2002.
- T. Tomita, “Immunocytochemical localization of glucose transporter-2 (Glut-2) in pancreatic islets and islet cell tumors,” Endocrine Pathology, vol. 10, no. 3, pp. 213–221, 1999.
- C. Doi, Y. Noguchi, T. Ito, T. Yoshikawa, T. Makino, and A. Matsumoto, “Alteration in immunoexpression of glucose transporter 2 in liver of tumour-bearing rats,” International Journal of Experimental Pathology, vol. 79, no. 1, pp. 25–31, 1998.
- H. K. Shim, W. W. Lee, S. Y. Park, H. Kim, Y. So, and S. E. Kim, “Expressions of glucose transporter types 1 and 3 and hexokinase-II in diffuse large B-cell lymphoma and other B-cell non-Hodgkin's lymphomas,” Nuclear Medicine and Biology, vol. 36, no. 2, pp. 191–197, 2009.
- S. Zhou, S. Wang, Q. Wu, J. Fan, and Q. Wang, “Expression of glucose transporter-1 and -3 in the head and neck carcinoma—the correlation of the expression with the biological behaviors,” ORL Journal for Otorhinolaryngology and Its Related Specialties, vol. 70, no. 3, pp. 189–194, 2008.
- L.-F. de Geus-Oei, J. H. van Krieken, R. P. Aliredjo, et al., “Biological correlates of FDG uptake in non-small cell lung cancer,” Lung Cancer, vol. 55, no. 1, pp. 79–87, 2007.
- T. Ito, Y. Noguchi, S. Satoh, H. Hayashi, Y. Inayama, and H. Kitamura, “Expression of facilitative glucose transporter isoforms in lung carcinomas: its relation to histologic type, differentiation grade, and tumor stage,” Modern Pathology, vol. 11, no. 5, pp. 437–443, 1998.
- C. Binder, L. Binder, D. Marx, A. Schauer, and W. Hiddemann, “Deregulated simultaneous expression of multiple glucose transporter isoforms in malignant cells and tissues,” Anticancer Research, vol. 17, no. 6, pp. 4299–4304, 1997.
- Z. Weihua, R. Tsan, W.-C. Huang, et al., “Survival of cancer cells is maintained by EGFR independent of its kinase activity,” Cancer Cell, vol. 13, no. 5, pp. 385–393, 2008.
- B. M. Helmke, C. Reisser, M. Idzkoe, G. Dyckhoff, and C. Herold-Mende, “Expression of SGLT-1 in preneoplastic and neoplastic lesions of the head and neck,” Oral Oncology, vol. 40, no. 1, pp. 28–35, 2004.
- V. F. Casneuf, P. Fonteyne, N. Van Damme, et al., “Expression of SGLT1, Bcl-2 and p53 in primary pancreatic cancer related to survival,” Cancer Investigation, vol. 26, no. 8, pp. 852–859, 2008.
- P.-R. Ling, R. J. Smith, and B. R. Bistrian, “Acute effects of hyperglycemia and hyperinsulinemia on hepatic oxidative stress and the systemic inflammatory response in rats,” Critical Care Medicine, vol. 35, no. 2, pp. 555–560, 2007.
- K. Esposito, F. Nappo, R. Marfella, et al., “Inflammatory cytokine concentrations are acutely increased by hyperglycemia in humans: role of oxidative stress,” Circulation, vol. 106, no. 16, pp. 2067–2072, 2002.
- F. Arnalich, A. Hernanz, D. Lopez-Maderuelo, et al., “Enhanced acute-phase response and oxidative stress in older adults with type II diabetes,” Hormone and Metabolic Research, vol. 32, no. 10, pp. 407–412, 2000.
- R. B. Ness, J. A. Grisso, C. Cottreau, et al., “Factors related to inflammation of the ovarian epithelium and risk of ovarian cancer,” Epidemiology, vol. 11, no. 2, pp. 111–117, 2000.
- R. B. Ness and C. Cottreau, “Possible role of ovarian epithelial inflammation in ovarian cancer,” Journal of the National Cancer Institute, vol. 91, no. 17, pp. 1459–1467, 1999.
- N. Auersperg, M. I. Edelson, S. C. Mok, S. W. Johnson, and T. C. Hamilton, “The biology of ovarian cancer,” Seminars in Oncology, vol. 25, no. 3, pp. 281–304, 1998.
- S. Huang, M. Van Arsdall, S. Tedjarati, et al., “Contributions of stromal metalloproteinase-9 to angiogenesis and growth of human ovarian carcinoma in mice,” Journal of the National Cancer Institute, vol. 94, no. 15, pp. 1134–1142, 2002.
- M. A. Nash, G. Ferrandina, M. Gordinier, A. Loercher, and R. S. Freedman, “The role of cytokines in both the normal and malignant ovary,” Endocrine-Related Cancer, vol. 6, no. 1, pp. 93–107, 1999.
- N. H. Obata, K. Tamakoshi, K. Shibata, F. Kikkawa, and Y. Tomoda, “Effects of Interleukin-6 on in vitro cell attachment, migration and invasion of human ovarian carcinoma,” Anticancer Research, vol. 17, no. 1, pp. 337–342, 1997.
- D. J. Satterwhite and H. L. Moses, “Mechanisms of transforming growth factor-beta1-induced cell cycle arrest,” Invasion and Metastasis, vol. 14, no. 1–6, pp. 309–318, 1994.
- W. Li, R. J. Xu, Z. Y. Lin, G. C. Zhuo, and H. H. Zhang, “Effects of a cyclooxygenase-1-selective inhibitor in a mouse model of ovarian cancer, administered alone or in combination with ibuprofen, a nonselective cyclooxygenase inhibitor,” Medical Oncology, vol. 26, no. 2, pp. 170–177, 2009.
- M. A. Altinoz and R. Korkmaz, “NF-B, macrophage migration inhibitory factor and cyclooxygenase-inhibitions as likely mechanisms behind the acetaminophen- and NSAID-prevention of the ovarian cancer,” Neoplasma, vol. 51, no. 4, pp. 239–247, 2004.
- H. A. Risch, “Hormonal etiology of epithelial ovarian cancer, with a hypothesis concerning the role of androgens and progesterone,” Journal of the National Cancer Institute, vol. 90, no. 23, pp. 1774–1786, 1998.
- J. Greenaway, R. Moorehead, P. Shaw, and J. Petrik, “Epithelial-stromal interaction increases cell proliferation, survival and tumorigenicity in a mouse model of human epithelial ovarian cancer,” Gynecologic Oncology, vol. 108, no. 2, pp. 385–394, 2008.
- J.-H. Choi, A. S. T. Wong, H.-F. Huang, and P. C. K. Leung, “Gonadotropins and ovarian cancer,” Endocrine Reviews, vol. 28, no. 4, pp. 440–461, 2007.
- M. B. Witte, T. Kiyama, and A. Barbul, “Nitric oxide enhances experimental wound healing in diabetes,” British Journal of Surgery, vol. 89, no. 12, pp. 1594–1601, 2002.
- M. T. Goova, J. Li, T. Kislinger, et al., “Blockade of receptor for advanced glycation end-products restores effective wound healing in diabetic mice,” American Journal of Pathology, vol. 159, no. 2, pp. 513–525, 2001.
- J. Folkman, “Tumor angiogenesis: therapeutic implications,” The New England Journal of Medicine, vol. 285, no. 21, pp. 1182–1186, 1971.
- E. C. Kohn, I. J. Fidler, D. Fishman, et al., “Discussion: metastasis and angiogenesis in epithelial ovarian cancer,” Gynecologic Oncology, vol. 88, pp. S37–S42, 2003.
- M. Schmidt, U. Kammerer, S. Segerer, et al., “Glucose metabolism and angiogenesis in granulosa cell tumors of the ovary: activation of Akt, expression of M2PK, TKTL1 and VEGF,” European Journal of Obstetrics Gynecology and Reproductive Biology, vol. 139, no. 1, pp. 72–78, 2008.
- L. E. Benjamin, “Glucose, VEGF-A, and diabetic complications,” American Journal of Pathology, vol. 158, no. 4, pp. 1181–1184, 2001.
- W.-L. Yeh, C.-J. Lin, and W.-M. Fu, “Enhancement of glucose transporter expression of brain endothelial cells by vascular endothelial growth factor derived from glioma exposed to hypoxia,” Molecular Pharmacology, vol. 73, no. 1, pp. 170–177, 2008.
- L. S. Angelo and R. Kurzrock, “Vascular endothelial growth factor and its relationship to inflammatory mediators,” Clinical Cancer Research, vol. 13, no. 10, pp. 2825–2830, 2007.
- J. Folkman, K. Watson, D. Ingber, and D. Hanahan, “Induction of angiogenesis during the transition from hyperplasia to neoplasia,” Nature, vol. 339, no. 6219, pp. 58–61, 1989.
- B. C. Cooper, J. M. Ritchie, C. L. W. Broghammer, et al., “Preoperative serum vascular endothelial growth factor levels: significance in ovarian cancer,” Clinical Cancer Research, vol. 8, no. 10, pp. 3193–3197, 2002.
- S. Huang, J. B. Robinson, A. DeGuzman, C. D. Bucana, and I. J. Fidler, “Blockade of nuclear factor-b signaling inhibits angiogenesis and tumorigenicity of human ovarian cancer cells by suppressing expression of vascular endothelial growth factor and interleukin 8,” Cancer Research, vol. 60, no. 19, pp. 5334–5339, 2000.
- M. Karin and F. R. Greten, “NF-B: linking inflammation and immunity to cancer development and progression,” Nature Reviews Immunology, vol. 5, no. 10, pp. 749–759, 2005.
- D. Belotti, P. Paganoni, L. Manenti, et al., “Matrix metalloproteinases (MMP9 and MMP2) induce the release of vascular endothelial growth factor (VEGF) by ovarian carcinoma cells: implications for ascites formation,” Cancer Research, vol. 63, no. 17, pp. 5224–5229, 2003.
- G. C. Kumaran, G. C. Jayson, and A. R. Clamp, “Antiangiogenic drugs in ovarian cancer,” British Journal of Cancer, vol. 100, no. 1, pp. 1–7, 2009.
- K. Grosios, J. Wood, R. Esser, A. Raychaudhuri, and J. Dawson, “Angiogenesis inhibition by the novel VEGF receptor tyrosine kinase inhibitor, PTK787/ZK222584, causes significant anti-arthritic effects in models of rheumatoid arthritis,” Inflammation Research, vol. 53, no. 4, pp. 133–142, 2004.
- R. S. Hundal, M. Krssak, S. Dufour, et al., “Mechanism by which metformin reduces glucose production in type 2 diabetes,” Diabetes, vol. 49, no. 12, pp. 2063–2069, 2000.
- V. N. Anisimov, L. M. Berstein, P. A. Egormin, et al., “Effect of metformin on life span and on the development of spontaneous mammary tumors in HER-2/neu transgenic mice,” Experimental Gerontology, vol. 40, no. 8-9, pp. 685–693, 2005.
- W. H. Gotlieb, J. Saumet, M.-C. Beauchamp, et al., “In vitro metformin anti-neoplastic activity in epithelial ovarian cancer,” Gynecologic Oncology, vol. 110, no. 2, pp. 246–250, 2008.
- M. C. Towler and D. G. Hardie, “AMP-activated protein kinase in metabolic control and insulin signaling,” Circulation Research, vol. 100, no. 3, pp. 328–341, 2007.
- J.-T. Cheng, C.-C. Huang, I.-M. Liu, T.-F. Tzeng, and C. J. Chang, “Novel mechanism for plasma glucose-lowering action of metformin in streptozotocin-induced diabetic rats,” Diabetes, vol. 55, no. 3, pp. 819–825, 2006.
- G. Zhou, R. Myers, Y. Li, et al., “Role of AMP-activated protein kinase in mechanism of metformin action,” Journal of Clinical Investigation, vol. 108, no. 8, pp. 1167–1174, 2001.
- W. Zhou, F. H. Wan, L. E. Landree, et al., “Fatty acid synthase inhibition activates AMP-activated protein kinase in SKOV3 human ovarian cancer cells,” Cancer Research, vol. 67, no. 7, pp. 2964–2971, 2007.
- J.-T. Hwang, D. Y. Kwon, O. J. Park, and M. S. Kim, “Resveratrol protects ROS-induced cell death by activating AMPK in H9c2 cardiac muscle cells,” Genes and Nutrition, vol. 2, no. 4, pp. 323–326, 2008.
- X. D. Zhang, E. Deslandes, M. Villedieu, et al., “Effect of 2-deoxy-D-glucose on various malignant cell lines in vitro,” Anticancer Research, vol. 26, no. 5, pp. 3561–3566, 2006.
- T. C. Hallstrom, S. Mori, and J. R. Nevins, “An E2F1-dependent gene expression program that determines the balance between proliferation and cell death,” Cancer Cell, vol. 13, no. 1, pp. 11–22, 2008.
- M. Jensterle, A. Janez, B. Mlinar, J. Marc, J. Prezelj, and M. Pfeifer, “Impact of metformin and rosiglitazone treatment on glucose transporter 4 mRNA expression in women with polycystic ovary syndrome,” European Journal of Endocrinology, vol. 158, no. 6, pp. 793–801, 2008.
- S. J. Lessard, S. L. Lo Giudice, W. Lau, et al., “Rosiglitazone enhances glucose tolerance by mechanisms other than reduction of fatty acid accumulation within skeletal muscle,” Endocrinology, vol. 145, no. 12, pp. 5665–5670, 2004.
- A. Aljada, L. O'Connor, Y.-Y. Fu, and S. A. Mousa, “PPAR ligands, rosiglitazone and pioglitazone, inhibit bFGF- and VEGF-mediated angiogenesis,” Angiogenesis, vol. 11, no. 4, pp. 361–367, 2008.
- L. Li, L. Wang, W. Zhang, et al., “Correlation of serum VEGF levels with clinical stage, therapy efficacy, tumor metastasis and patient survival in ovarian cancer,” Anticancer Research, vol. 24, no. 3, pp. 1973–1979, 2004.
- E. S. Bamberger and C. W. Perrett, “Angiogenesis in epithelial ovarian cancer,” Molecular Pathology, vol. 55, pp. 348–359, 2002.