Seo Jieun, Jeong Do-Won, Park Jong-Wan, Lee Kwang-Woong, Fukuda Junji, Chun Yang-Sook
Department of Biomedical Sciences, Seoul National University College of Medicine, Seoul, 03080, South Korea.
Department of Physiology, Seoul National University College of Medicine, Seoul, 03080, South Korea.
Commun Biol. 2020 Oct 30;3(1):638. doi: 10.1038/s42003-020-01367-5.
Hypoxia-inducible factor-1 alpha (HIF-1α) is a transcription factor essential for cancer cell survival. The reprogramming of lipid metabolism has emerged as a hallmark of cancer, yet the relevance of HIF-1α to this process remains elusive. In this study, we profile HIF-1α-interacting proteins using proteomics analysis and identify fatty acid-binding protein 5 (FABP5) as a critical HIF-1α-binding partner. In hepatocellular carcinoma (HCC) tissues, both FABP5 and HIF-1α are upregulated, and their expression levels are associated with poor prognosis. FABP5 enhances HIF-1α activity by promoting HIF-1α synthesis while disrupting FIH/HIF-1α interaction at the same time. Oleic-acid treatment activates the FABP5/HIF-1α axis, thereby promoting lipid accumulation and cell proliferation in HCC cells. Our results indicate that fatty-acid-induced FABP5 upregulation drives HCC progression through HIF-1-driven lipid metabolism reprogramming.
缺氧诱导因子-1α(HIF-1α)是癌细胞存活所必需的转录因子。脂质代谢重编程已成为癌症的一个标志,然而HIF-1α与这一过程的相关性仍不清楚。在本研究中,我们通过蛋白质组学分析对与HIF-1α相互作用的蛋白质进行了分析,并确定脂肪酸结合蛋白5(FABP5)是关键的HIF-1α结合伴侣。在肝细胞癌(HCC)组织中,FABP5和HIF-1α均上调,且它们的表达水平与不良预后相关。FABP5通过促进HIF-1α合成增强HIF-1α活性,同时破坏FIH/HIF-1α相互作用。油酸处理激活FABP5/HIF-1α轴,从而促进HCC细胞中的脂质积累和细胞增殖。我们的结果表明,脂肪酸诱导的FABP5上调通过HIF-1驱动的脂质代谢重编程推动HCC进展。