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Hypoxia and angiogenesis: regulation of hypoxia-inducible factors via novel binding factors

机译:缺氧和血管生成:通过新型结合因子调节缺氧诱导因子

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The mechanisms that regulate angiogenesis in hypoxia or hypoxic microenvironment are modulated by several pro- and antiangiogenic factors. Hypoxia-inducible factors (HIFs) have been established as the basic and major inducers of angiogenesis, but understanding the role of interacting proteins is becoming increasingly important to elucidate the angiogenic processes of a hypoxic response. In particular, with regard to wound healing and the novel therapies for vascular disorders such as ischemic brain and heart attack, it is essential to gain insights in the formation and regulation of HIF transcriptional machineries related to angiogenesis. Further, identification of alternative ways of inhibiting tumor growth by disrupting the growth-triggering mechanisms of increasing vascular supply via angiogenesis depends on the knowledge of how tumor cells develop their own vasculature. Here, we review our findings on the interactions of basic HIFs, HIF-1α and HIF-2α, with their regulatory binding proteins, histone deacetylase 7 (HDAC7) and translation initiation factor 6 (Int6), respectively. The present results and discussion revealed new regulatory interactions of HIF-related mechanisms.
机译:在缺氧或缺氧的微环境中调节血管生成的机制受到几种促血管生成因子和抗血管生成因子的调节。缺氧诱导因子(HIFs)已被确定为血管生成的基本和主要诱导剂,但是了解相互作用蛋白的作用对于阐明低氧反应的血管生成过程变得越来越重要。特别地,关于伤口愈合和针对诸如缺血性脑和心脏病发作的血管疾病的新疗法,必不可少的是在与血管生成有关的HIF转录机制的形成和调控中获得见识。此外,通过破坏经由血管生成增加血管供应的生长触发机制来抑制肿瘤生长的替代方法的鉴定取决于对肿瘤细胞如何发展其自身脉管系统的了解。在这里,我们回顾我们关于基本HIF,HIF-1α和HIF-2α与它们的调节结合蛋白,组蛋白脱乙酰基酶7(HDAC7)和翻译起始因子6(Int6)相互作用的发现。目前的结果和讨论揭示了HIF相关机制的新监管相互作用。

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