Qinghai University, Xining 810001, PR China; Qinghai Provincial People's Hospital, Xining 810001, PR China.
Qinghai Provincial People's Hospital, Xining 810001, PR China.
Cell Signal. 2024 Oct;122:111328. doi: 10.1016/j.cellsig.2024.111328. Epub 2024 Jul 31.
Ferroptosis is a novel, iron-dependent cell death characterized by the excessive accumulation of ferroptosis lipid peroxides ultimately leading to oxidative damage to the cell membrane. Iron, lipid, amino acid metabolism, and other signaling pathways all control ferroptosis. Numerous bodily tissues experience hypoxia under normal and pathological circumstances. Tissue cells can adjust to these changes by activating the hypoxia-inducible factor (HIF) signaling pathway and other mechanisms in response to the hypoxic environment. In recent years, there has been increasing evidence that hypoxia and ferroptosis are closely linked, and that hypoxia can regulate ferroptosis in specific cells and conditions through different pathways. In this paper, we review the possible positive and negative regulatory mechanisms of ferroptosis by hypoxia-inducible factors, as well as ferroptosis-associated ischemic diseases, with the intention of delivering novel therapeutic avenues for the defense and management of hypoxic illnesses linked to ferroptosis.
铁死亡是一种新型的、依赖于铁的细胞死亡方式,其特征是铁死亡脂质过氧化物的过度积累,最终导致细胞膜的氧化损伤。铁、脂质、氨基酸代谢和其他信号通路都控制着铁死亡。在正常和病理情况下,许多身体组织都会经历缺氧。组织细胞可以通过激活缺氧诱导因子 (HIF) 信号通路和其他机制来适应缺氧环境。近年来,越来越多的证据表明缺氧和铁死亡密切相关,缺氧可以通过不同的途径在特定的细胞和条件下调节铁死亡。在本文中,我们综述了缺氧诱导因子对铁死亡的可能正、负调节机制,以及与铁死亡相关的缺血性疾病,以期为与铁死亡相关的缺氧性疾病的防治提供新的治疗途径。