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酶15-脂氧合酶1促进缺氧诱导因子1α的周转并降低血管内皮生长因子的表达:对血管生成的影响。

Enzyme 15-lipoxygenase 1 promotes hypoxia-inducible factor 1α turnover and reduces vascular endothelial growth factor expression: implications for angiogenesis.

作者信息

Zhong Hua, Wang Ruoxiang, Kelavkar Uddhav, Wang Christopher Y, Simons Jonathan

机构信息

Department of Urology and Winship Cancer Institute, Emory University School of Medicine, Atlanta, Georgia, 30322; Rutgers Cancer Institute of New Jersey and Department of Pathology and Laboratory Medicine, Rutgers Robert Wood Johnson Medical School, New Brunswick, New Jersey, 08901.

出版信息

Cancer Med. 2014 Jun;3(3):514-25. doi: 10.1002/cam4.227. Epub 2014 Mar 25.

Abstract

Hypoxia-inducible factor 1α (HIF-1α) is the regulatory subunit of the heterodimeric HIF-1 that plays a critical role in transcriptional regulation of genes in angiogenesis and hypoxic adaptation, while fatty acid metabolism mediated by lipoxygenases has been implicated in a variety of pathogeneses, including cancers. In this study, we report that 15-lipoxygenase 1 (15-LO1), a key member of the lipoxygenase family, promotes HIF-1α ubiquitination and degradation. Altering the level of 15-LO1 yields inverse changes in HIF-1α and HIF-1 transcriptional activity, under both normoxia and hypoxia, and even in CoCl2 -treated cells where HIF-1α has been artificially elevated. The antagonistic effect of 15-LO1 is mediated by the Pro(564) /hydroxylation/26S proteasome system, while both the enzymatic activity and the intracellular membrane-binding function of 15-LO1 appear to contribute to HIF-1α suppression. Our findings provide a novel mechanism for HIF-1α regulation, in which oxygen-dependent HIF-1 activity is modulated by an oxygen-insensitive lipid metabolic enzyme.

摘要

缺氧诱导因子1α(HIF-1α)是异二聚体HIF-1的调节亚基,在血管生成和缺氧适应过程中基因的转录调控中起关键作用,而脂氧合酶介导的脂肪酸代谢与包括癌症在内的多种发病机制有关。在本研究中,我们报告脂氧合酶家族的关键成员15-脂氧合酶1(15-LO1)可促进HIF-1α的泛素化和降解。在常氧和缺氧条件下,甚至在HIF-1α已被人为升高的氯化钴处理的细胞中,改变15-LO1的水平会导致HIF-1α和HIF-1转录活性发生相反的变化。15-LO1的拮抗作用由Pro(564)/羟基化/26S蛋白酶体系统介导,而15-LO1的酶活性和细胞内膜结合功能似乎都有助于抑制HIF-1α。我们的发现为HIF-1α调控提供了一种新机制,其中氧依赖性HIF-1活性由氧不敏感的脂质代谢酶调节。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bce0/4101742/4d6750d00cdd/cam40003-0514-f1.jpg

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