缺氧在癌症进展、血管生成、转移和治疗抵抗中的作用

B. Muz, P. de la Puente, F. Azab, A. Azab
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引用次数: 1199

摘要

缺氧是一种非生理水平的氧张力,是大多数恶性肿瘤中常见的现象。肿瘤缺氧导致晚期但功能失调的血管形成和上皮-间质转化表型的获得,从而导致细胞的移动和转移。缺氧改变了癌细胞的代谢,并通过诱导细胞静止来促进治疗抵抗。缺氧刺激癌细胞中复杂的细胞信号网络,包括HIF、PI3K、MAPK和NFĸB通路,它们相互作用,形成正负反馈循环,增强或减弱缺氧作用。本文综述了肿瘤缺氧的作用以及HIF细胞信号在肿瘤血管形成、转移和耐药发展中的作用。更好地了解缺氧在癌症进展中的作用,将为发现针对缺氧肿瘤细胞和缺氧微环境的新疗法打开新的窗口。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The role of hypoxia in cancer progression, angiogenesis, metastasis, and resistance to therapy
Hypoxia is a non-physiological level of oxygen tension, a phenomenon common in a majority of malignant tumors. Tumor-hypoxia leads to advanced but dysfunctional vascularization and acquisition of epithelial-to-mesenchymal transition phenotype resulting in cell mobility and metastasis. Hypoxia alters cancer cell metabolism and contributes to therapy resistance by inducing cell quiescence. Hypoxia stimulates a complex cell signaling network in cancer cells, including the HIF, PI3K, MAPK, and NFĸB pathways, which interact with each other causing positive and negative feedback loops and enhancing or diminishing hypoxic effects. This review provides background knowledge on the role of tumor hypoxia and the role of the HIF cell signaling involved in tumor blood vessel formation, metastasis, and development of the resistance to therapy. Better understanding of the role of hypoxia in cancer progression will open new windows for the discovery of new therapeutics targeting hypoxic tumor cells and hypoxic microenvironment.
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