Biocenter Oulu, Faculty of Biochemistry and Molecular Medicine, Oulu Center for Cell-Matrix Research, University of Oulu, Oulu, Finland.
Faculty of Biochemistry and Molecular Medicine, University of Oulu, Oulu, Finland.
Trends Mol Med. 2018 Dec;24(12):1021-1035. doi: 10.1016/j.molmed.2018.10.004. Epub 2018 Nov 1.
Hypoxia-inducible factor prolyl 4-hydroxylases (HIF-P4Hs, also known as PHDs or EglNs) are enzymes that act as cellular oxygen sensors. Inhibition of HIF-P4Hs leads to stabilization of hypoxia-inducible transcription factors (HIFs), which initiates a gene expression program that allows organisms to cope with low oxygen levels and restore tissue oxygenation. This involves, for example, upregulation of erythropoiesis and angiogenesis, modulation of inflammatory responses, and reprogramming of metabolism. Currently, several pharmacological HIF-P4H inhibitors are in clinical trials mainly for renal anemia. However, recent data suggest that HIF-P4H inhibitors could also be considered to treat metabolic disorders. Here, we discuss the potential of targeting HIF-P4Hs and the HIF pathway for the treatment of obesity, metabolic syndrome, atherosclerosis, and fatty liver diseases (FLDs).
缺氧诱导因子脯氨酰 4-羟化酶(HIF-P4Hs,也称为 PHD 或 EglNs)是作为细胞氧传感器的酶。HIF-P4Hs 的抑制导致缺氧诱导转录因子(HIFs)的稳定化,从而启动允许生物体应对低氧水平并恢复组织氧合的基因表达程序。这涉及例如红细胞生成和血管生成的上调、炎症反应的调节以及代谢的重编程。目前,几种药理学 HIF-P4H 抑制剂正在临床试验中,主要用于治疗肾性贫血。然而,最近的数据表明,HIF-P4H 抑制剂也可被考虑用于治疗代谢紊乱。在这里,我们讨论了针对 HIF-P4Hs 和 HIF 途径治疗肥胖症、代谢综合征、动脉粥样硬化和脂肪肝疾病(FLDs)的潜力。