首页> 美国卫生研究院文献>Medical Science Monitor : International Medical Journal of Experimental and Clinical Research >Knockdown of Hypoxia-Inducible Factor 1α (HIF-1α) Promotes Autophagy and Inhibits Phosphatidylinositol 3-Kinase (PI3K)/AKT/Mammalian Target of Rapamycin (mTOR) Signaling Pathway in Ovarian Cancer Cells
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Knockdown of Hypoxia-Inducible Factor 1α (HIF-1α) Promotes Autophagy and Inhibits Phosphatidylinositol 3-Kinase (PI3K)/AKT/Mammalian Target of Rapamycin (mTOR) Signaling Pathway in Ovarian Cancer Cells

机译:敲低缺氧诱导因子1α(HIF-1α)促进自噬并抑制卵巢癌细胞中雷帕霉素(mTOR)信号通路的磷脂酰肌醇3-激酶(PI3K)/ AKT /哺乳动物靶标

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摘要

BackgroundOvarian cancer has the highest mortality rate among all female genital tumors because of its insidious onset and drug resistance. Hypoxia-inducible factor 1α (HIF-1α), one of the best-studied oncogenes, plays an important part in tumor adaptation to microenvironmental hypoxia and was found to be overexpressed in several malignancies, including ovarian cancer. Previous studies found that the effect of HIF-1α on cancers may be correlated with autophagy and some signaling pathways, such as PI3K/AKT/mTOR, in several tumors. However, the function and potential mechanism have not been clearly defined.
机译:背景技术由于其隐匿的发病率和耐药性,卵巢癌在所有女性生殖器肿瘤中死亡率最高。缺氧诱导因子1α(HIF-1α)是研究最深入的致癌基因之一,在肿瘤对微环境缺氧的适应中起着重要作用,并发现在包括卵巢癌在内的多种恶性肿瘤中过表达。先前的研究发现,HIF-1α对癌症的影响可能与自体吞噬和某些肿瘤中的某些信号通路(例如PI3K / AKT / mTOR)相关。但是,功能和潜在机制尚未明确定义。

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