Zhong Hua, Wang Ruoxiang, Kelavkar Uddhav, Wang Christopher Y, Simons Jonathan
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.
Cancer Med. 2014 Jun;3(3):514-25. doi: 10.1002/cam4.227. Epub 2014 Mar 25.
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.
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。