The Role of Hypoxia in Endometrial Cancer
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Endometrial cancer represents the most frequent neoplasia from the corpus uteri and comprises the 14th leading cause of death in women worldwide. Risk factors that contribute to the disease include early menarche, late menopause, nulliparity, and menopausal hormone use, as well as hypertension and obesity comorbidities. The clinical effectiveness of chemotherapy is variable, suggesting that novel molecular targeted therapies against specific cellular processes associated with the maintenance of cancer cell survival and therapy resistance ameliorate the rates of success in endometrial cancer treatment. In the course of tumor growth, cancer cells must adapt to decreased oxygen availability in the microenvironment by upregulation of hypoxia-inducible factors, which orchestrate the activation of a transcriptional program leading to cell survival. During this adaptative process, the hypoxic cancer cells may acquire invasive and metastatic properties as well as increased cell proliferation and resistance to chemotherapy, enhanced angiogenesis, vasculogenic mimicry, and maintenance of cancer cell stemness, which contribute to more aggressive cancer phenotypes. Several studies have shown that hypoxia-inducible factor 1 alpha (HIF-1α) protein is aberrantly overexpressed in many solid tumors of the breast, prostate, ovarian, bladder, colon, brain, and pancreas. Thus, it has been considered an important therapeutic target. Here, we reviewed the current knowledge of the relevant roles of cellular hypoxia mechanisms and HIF-1α functions in diverse processes associated with endometrial cancer progression. In addition, we also summarize the role of microRNAs in the posttranscriptional regulation of protein-encoding genes involved in the hypoxia response in endometrial cancer. Finally, we pointed out the need for urgent targeted therapies to impair the cellular processes activated by hypoxia in the tumor microenvironment. © 2022 Bentham Science Publishers.
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chemotherapy; Endometrial cancer; HIF-1α; hypoxia; microRNAs; therapy 6 n methyladenosine; angiopoietin related protein 4; argonaute 2 protein; carbonate dehydratase IX; cyclin dependent kinase; cyclooxygenase 2; cysteine rich protein 61; DNA (cytosine 5) methyltransferase 1; DNA mismatch repair protein MSH2; estrogen receptor; fibroblast growth factor 9; glucose transporter 1; hypoxia inducible factor 1alpha; leptin; microRNA; microRNA 210; mismatch repair protein PMS2; mitogen activated protein kinase; MutL protein homolog 1; octamer transcription factor 4; phosphatidylinositol 3,4,5 trisphosphate 3 phosphatase; procollagen proline 2 oxoglutarate 4 dioxygenase; progesterone receptor; protein bcl 2; protein BNip3; protein MSH6; protein p27; reactive oxygen metabolite; somatomedin C receptor; transcription factor NANOG; transcription factor Snail; transcription factor Sox2; transcription factor Twist; Twist related protein 1; uvomorulin; vasculotropin; von Hippel Lindau protein; hypoxia inducible factor 1alpha; microRNA; cancer growth; cell proliferation; cell viability; endometrium cancer; epithelial mesenchymal transition; female; gene overexpression; gene silencing; high throughput sequencing; human; hypertension; menopause; molecularly targeted therapy; nuclear reprogramming; nullipara; obesity; oxidative stress; phenotype; protein degradation; protein expression; Review; risk factor; transcription regulation; tumor growth; tumor hypoxia; tumor microenvironment; cell hypoxia; endometrium tumor; hypoxia; male; tumor cell line; Cell Hypoxia; Cell Line, Tumor; Cell Proliferation; Endometrial Neoplasms; Female; Humans; Hypoxia; Hypoxia-Inducible Factor 1, alpha Subunit; Male; MicroRNAs; Tumor Microenvironment
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