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Anat Cell Biol. Jun 2012; 45(2): 73–78.
Published online Jun 30, 2012. doi:  10.5115/acb.2012.45.2.73
PMCID: PMC3398177
From tumor hypoxia to cancer progression: the implications of hypoxia-inducible factor-1 expression in cancers
Fariz Nurwidya,corresponding author Fumiyuki Takahashi, Kunihiko Minakata, Akiko Murakami, and Kazuhisa Takahashi
Department of Respiratory Medicine, Juntendo University School of Medicine, Tokyo, Japan.
corresponding authorCorresponding author.
Corresponding author: Fariz Nurwidya. Department of Respiratory Medicine, Juntendo University School of Medicine, 2-1-1 Hongo, Bunkyo-ku, Tokyo 113-8421, Japan. Tel: +81-80-3690-2529, Fax: +81-3-5802-1617, fariz/at/juntendo.ac.jp
Received March 9, 2012; Accepted May 14, 2012.
Hypoxia, defined as a decrease of tissue oxygen levels, represents a fundamental pathophysiological condition in the microenvironment of solid tumors. Tumor hypoxia is known to be associated with radio/chemo-resistance and metastasis that eventually lead to cancer progression contributing to poor prognosis in cancer patients. Among transcription factors that accumulated under hypoxic conditions, hypoxia-inducible factor-1 (HIF-1) is a master transcription factor that has received the most intense attention in this field of research due to its capacity to modulate several hundred genes. With a clearer understanding of the HIF-1 pathway, efforts are directed at manipulation of this complex genetic process in order to ultimately decrease cellular HIF-1 levels. Some novel agents have been shown to have HIF-1 inhibition activity through a variety of molecular mechanisms and have provided promising results in the preclinical setting.
Keywords: Tumor hypoxia, Cancer progression, Hypoxia-inducible factor-1
To grow beyond a diameter of approximately 1 mm, newly developing tumors must form their own vascular network and blood supply [1]. Angiogenesis is an adaptive response to tissue hypoxia [2]. Compared with the regular, ordered vasculature of normal tissues, blood vessels in tumors are often highly abnormal, with distended capillaries, leaky walls, and sluggish flow [3]. Tissue hypoxia results when supply of oxygen from the bloodstream does not meet demand from the cells in the tissue [4]. Protection against hypoxia in solid tumors is an important step in tumor development and progression [5].
The beginnings of hypoxia research in tumor biology can be traced back to observations made in the early 20th century by Otto Warburg, who demonstrated that, unlike normal cells, tumor cells favor glycolysis, independent of cellular oxygenation levels [6].
Physiologists and clinicians define hypoxia as a state of reduced O2 availability or decreased O2 partial pressures below critical thresholds, thus restricting or even abolishing the function of organs, tissues, or cells [7]. Other investigators define hypoxia as areas with O2 tensions (pO2 values)≤2.5 mm Hg [8].
Hypoxia was initially studied because of its effects on responses to radiotherapy. Radiation treatment requires free radicals from oxygen to destroy target cells, and cells in hypoxic areas were found to be resistant to radiation-induced cell death [9]. Hypoxia alters the behavior of tumor cells through a number of O2-sensitive pathways and the best understood pathway is that mediated by the hypoxia-inducible factor family of transcription factors (HIFs) [10]. Activation of HIF in cancer has been shown to contribute to the classical tumor phenotypes of upregulated glycolysis and angiogenesis, leading to widespread interest in the HIF system as a target in cancer therapeutics [11]. Furthermore, studies indicate that hypoxia promotes genetic instability that leads to tumor progression [12]. Putra et al. [13] has provided evidence that functional polymorphisms in the HIF-1α gene may have an important impact on lung carcinogenesis, especially in adenocarcinomas, possibly by increasing genomic instability.
To date, three HIFs (HIF-1, HIF-2, and HIF-3) have been identified as regulating transcriptional programs in response to low oxygen levels [14]. HIF-1α is expressed ubiquitously in all cells, whereas HIF-2α and HIF-3α are selectively expressed in certain tissues, including vascular endothelial cells, type II pneumocytes, renal interstitial cells, liver parenchymal cells, and cells of the myeloid lineage [15].
HIF-1 is a heterodimeric protein that is composed of HIF-1α and HIF-1β subunits. The amino terminal half of each subunit consists of basic helix-loop-helix and Per-ARNT-Sim (PAS) domains that mediate heterodimerization and DNA binding [16]. HIF-1α is subjected to O2-dependent hydroxylation on proline residue 402 and/or 564 by prolyl hydroxylase domain protein 2 and this modification creates an interface for interaction with the von Hippel-Lindau tumor suppressor protein, which recruits an E3 ubiquitin-protein ligase that catalyzes polyubiquitination of HIF-1α, thereby targeting it for proteasomal degradation [17]. During hypoxia, HIF-1α is stabilized and dimerized with HIF-1β, and the complex is translocated into the nucleus where it binds to hypoxia-responsive elements in the promoters or enhancers of the target genes, such as the genes encoding erythropoetin, glucose transporters, glycolytic enzymes, hemeoxygenase-1, inducible nitric oxide synthase, transferrin, and vascular endothelial growth factor (VEGF) [18]. HIF-1α protein expression is likely to be particularly sensitive to changes in the rate of synthesis because of its extremely short half-life under non-hypoxic conditions [19].
HIF-2α has been associated with, and appears to promote, an undifferentiated phenotype in pluripotential cells [20]. HIF-2α (also known as EPAS-1, HLF) facilitates oxygen delivery and cellular adaptation to hypoxia by stimulating erythropoiesis, angiogenesis, and anaerobic glucose metabolism [21]. It has been shown that HIF-2α binds to the Oct-4 promoter and induces Oct-4 expression and transcriptional activity, thereby contributing to impaired development in homozygous HIF-2α KI/KI embryos, defective hematopoietic stem cell differentiation in embryoid bodies, and large embryonic stem cell-derived tumors characterized by altered cellular differentiation [22]. Furthermore, tumor hypoxia/HIF2α activation elicits an increase in epidermal growth factor receptor (EGFR) protein synthesis, and hence receptor expression, that is required for tumor cell growth autonomy [23].
HIF-3α is expressed abundantly in lung epithelial cells, and the transcriptional induction of HIF-3α plays an important role in the response to hypoxia in vitro [24]. Moderate hypoxia induced mRNA transcription of HIF-3α whereas HIF-1α and HIF-2α mRNA levels remained unchanged [25]. As a very sensitive and rapidly reacting component of the HIF system, HIF-3α may therefore contribute to protection during early intervals of hypoxia and/or moderate hypoxia, while, in contrast, HIF-1α and HIF-2α may confer protection against severe and/or prolonged hypoxia [25].
Tumor hypoxia has two sides. On the one hand, tissue O2 concentrations of <1% (pO2<7 mm Hg) exert antiproliferative effects, restrict cell proliferation, promote differentiation, and may induce apoptosis and necrosis [26]. On the other hand, hypoxia is known to promote aggressive phenotypes of tumor and induces their invasiveness and metastasis [27]. When PC-3 cells and prostate cancer cell lines were exposed to 1% oxygen (hypoxia) for various periods of time, chronic hypoxia (≥24 hours) decreased cell proliferation and induced cell death. In contrast, the prostate cancer cells exposed to acute hypoxia (≤6 hours) displayed increased motility, clonogenic survival, and invasive capacity [28].
The upregulation of HIF-1 is considered the molecular "switch" or "event" that is turned on by hypoxia [29]. However, stimulation of cells with a variety of growth factors and cytokines, including epidermal growth factor, fibroblast growth factor-2, heregulin, insulin, insulin-like growth factor 1 and 2, and interleukin-1b also induce the expression of HIF-1α protein, HIF-1 DNA-binding activity, and HIF-1 target gene expression under non-hypoxic conditions [30].
As HIF-1 is a central transcription factor, once it is being upregulated, it will subsequently modulate the expression of many genes involved in cell metabolism, proliferation, apoptosis, and angiogenesis [31]. Recently, large-scale microarray approaches indicate that HIF-1 activates hundreds of target genes [32]. Activating HIF-1 usually means increased nuclear-HIF-1α expression. Although nuclear-HIF-1α expression has been reported to be the master of transcription factor, some study also revealed the importance of cytoplasmic-HIF-1α expression [33].
Severe and prolonged hypoxia may initiate apoptosis, whereas under acute and mild hypoxia, cells may adapt to this environmental stress and will survive [34]. Mounting evidence also suggests that hypoxic induces metastasis of hypoxia-surviving cancer cells. Cancer metastasis is mediated by the epithelial mesenchymal transition (EMT) process, by which cancer cells loss its epithelial markers and gain its mesencymal markers [35]. Loss or reduction of E-cadherin, an epithelial marker, expression is frequently observed at the invasive front of many advanced-stage human carcinomas [36]. Several lines of evidence suggest that hypoxia may be an important factor contributing to the loss of E-cadherin in solid tumors [37].
Hypoxia has also led to therapeutic resistance through: 1) direct effects due to a lack of O2 which some drugs and radiation require to be maximally cytotoxic; 2) indirect effects via altered cellular metabolism which decreases drug cytotoxicity, and; 3) enhanced genetic instability which can lead to more rapid development of drug resistant tumor cells [38]. The chemoresistance of hypoxic regions is a consequence, at least in part, of the low accessibility of the drug to these areas due to their poor vascularization [39]. As for radiotherapy, the biological effect of radiation depends on the degree of oxygenation, and hypoxic cells are approximately three-fold more resistant than well-oxygenated cells [40]. In one study, it has been demonstrated that hypoxia-induced chemoresistance to cisplatin and doxorubicin in non-small cell lung cancer (NSCLC) cells is through the HIF pathway and silencing of the HIF-1α gene reverses these drugs' resistance [41].
Recently, HIFs have been shown to activate specific signaling pathways such as Notch and activate the expression of transcription factors such as Oct-4 that control stem cell self-renewal and multipotency [42]. It has been reported that embryonal carcinoma cell lines showed faster proliferation when the culture was carried out under hypoxic (5% O2) vs. normal (21% O2) conditions [43].
Using a novel cycling hypoxia-selected subpopulation from human breast cancer cell lines, Louie et al. [44] demonstrated that a stem-like breast cancer cell subpopulation could be expanded through repetitive hypoxia/reoxygenation cycles without genetic manipulation. They also discovered that cells derived from this subpopulation can form colonies readily, are highly tumorigenic in immune-deficient mice, and exhibit both stem-like and EMT phenotypes [44].
With a clearer understanding of the HIF-1 pathway, efforts are directed at manipulation of this complex genetic process in order to ultimately decrease cellular HIF-1 levels. Inhibition of HIF-1 in animal model systems manifests decrease in tumorigenesis and increase in survival [45]. As HIF-1 has been found to regulate the shift within the tumor cells to anaerobic metabolism and to activate VEGF and angiogenesis, downregulation of the HIF-1 complex may suppress cancer progression [46]. Many approaches have been made to inhibit the expression or the transcriptional activity of HIF-1, such as genetic approaches and pharmacological approaches [47]. Meanwhile, there is a group of hypoxia-activated prodrugs, which preferentially form cytotoxic and DNA-damaging free radicals under hypoxia, thus selectively eradicating hypoxic cells [48]. According to their putative mechanism of action, HIF-1 inhibitors could be tentatively divided into agents that modulate: 1) HIF-1α DNA binding; 2) HIF-1α mRNA expression; 3) HIF-1α protein degradation; 4) HIF-1α transcriptional activity; and 5) HIF-1α protein translation [49].
HIF-1α DNA Binding Inhibition
Doxorubicin is known to have HIF-1 inhibition activity by blocking its binding to DNA [50]. Wang et al. [51] proposed a complex drug delivery system consisting of liposomes as a nano-carrier, doxorubicin as a cell death inducer, and antisense oligonucleotides targeted to HIF-1α mRNA as a suppressor of cellular resistance and angiogenesis. The system effectively delivers active ingredients into tumor cells, multiplies the cell death signal initiated by doxorubicin, and inhibits cellular defensive mechanisms and angiogenesis.
HIF-1α mRNA Expression Inhibition
EZN-2968 is a RNA antagonist composed of a third-generation oligonucleotide that specifically binds and inhibits the expression of HIF-1α mRNA [52]. EZN-2968 has been reported to induce a potent, selective, and durable antagonism of HIF-1 mRNA and protein expression (IC50, 1-5 nmol/L) under normoxic and hypoxic conditions associated with inhibition of tumor cell growth [52]. Another agent that disrupts HIF-1α mRNA expression is aminoflavone. Aminoflavone is a ligand of the aryl hydrocarbon receptor that has been shown to inhibit HIF-1α mRNA expression by ~50% [53].
HIF-1α Protein Degradation
EGFR tyrosine kinase inhibitor, gefitinib, has been shown to circumvent hypoxia-induced drug (cisplatin, paclitaxel and gemcitabine) resistance via the regulation of HIF-1α expression [54]. This action of gefitinib was caused by reduced protein stability without any change in the level of HIF-1α mRNA. Interestingly, downregulation of HIF-1α has also been associated with positive therapeutic responses of cancer cells to EGFR-targeted therapy [55].
Rapamycin has been shown to induce apoptosis in NSCLC cell lines through downregulation of survivin under hypoxic condition [56]. Pretreatment of PC-3 cells and prostate cancer cell lines with the rapamycin inhibited both the accumulation of HIF-1α and HIF-1-dependent transcriptional activity [57]. Another active substance that might fall into this 'transcription-inhibition category' is chetomin. Chetomin, a dithiodiketopiperazine metabolite of the fungus Chaetomium species, was known to have antimicrobial activity [58]. Systemic administration of chetomin inhibited hypoxia-inducible transcription within tumors and inhibited tumor growth [59]. Meanwhile P3155, an HIF-1α inhibitor with antiangiogenic activity, showed specific HIF-1α inhibition with IC50 of 1.4 µM under hypoxia [60]. It suppressed HIF-1α expression as well as the phosphatidylinositol-3-kinase/Akt pathway and abrogated expression of the HIF-1-inducible gene [60].
Selective inhibition of HIF-1 activation by using HIF-1α-targeted siRNA treatment reduces hypoxic radioresistance in vitro as effectively as a pharmacologic approach with chetomin as a small molecule blocking the HIF pathway [61]. In another study, HIF-1α siRNA-transfected glioma cell lines have decreased growth both in vitro and in vivo as well as proliferative index [62].
Inhibition of HIF-1 has not always about therapeutic domain. Some studies have also investigated the possible benefit of HIF-1 inhibition for cancer prevention. Several natural products (e.g., resveratrol, genistein, apigenin, and berberin) have also been found to inhibit the activity of HIF-1 [63]. However, the use of HIF-1 inhibitors in cancer chemoprevention might be associated with toxicity [63].
Hypoxia is a common pathophysiological occurrence with a profound impact on the cellular transcriptome [64], and is undoubtedly an important mechanism of HIF activation in tumors [65]. HIF-1 is a master regulator of various target genes that plays critical roles in a multitude of pathways involved in the progression of cancer. The discovery of HIF-1 has increased enthusiasm for the investigation and development of targeted therapies modulating the cancer cell's response to the hypoxic microenvironment. Despite further needs of preclinical and clinical validation, HIF-1-targeted therapies, combined with radiotherapy and chemotherapy, are expected to be included in an integrated approach to cancer therapy in the future.
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