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缺氧与铁死亡。

Hypoxia and ferroptosis.

机构信息

Qinghai University, Xining 810001, PR China; Qinghai Provincial People's Hospital, Xining 810001, PR China.

Qinghai Provincial People's Hospital, Xining 810001, PR China.

出版信息

Cell Signal. 2024 Oct;122:111328. doi: 10.1016/j.cellsig.2024.111328. Epub 2024 Jul 31.

DOI:10.1016/j.cellsig.2024.111328
PMID:39094672
Abstract

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.

摘要

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。

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Cell Signal. 2024 Oct;122:111328. doi: 10.1016/j.cellsig.2024.111328. Epub 2024 Jul 31.
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Ferroptosis: a key driver and therapeutic target in the pathogenesis of acute respiratory distress syndrome.铁死亡:急性呼吸窘迫综合征发病机制中的关键驱动因素和治疗靶点。
Front Immunol. 2025 Jul 22;16:1567980. doi: 10.3389/fimmu.2025.1567980. eCollection 2025.
2
Nano-orchestrated magnetotactic-like navigation for electromagnetic theranostics and immune enhancement via photoautotrophic oxygenation, mild hyperthermia, and ferroptosis.通过光合自养氧合、温和热疗和铁死亡实现用于电磁诊疗和免疫增强的纳米编排类趋磁导航。
J Nanobiotechnology. 2025 Jun 13;23(1):442. doi: 10.1186/s12951-025-03488-7.
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Mechanism of Mitophagy to Protect Yak Kidney from Hypoxia-Induced Fibrosis Damage by Regulating Ferroptosis Pathway.
线粒体自噬通过调节铁死亡途径保护牦牛肾脏免受缺氧诱导的纤维化损伤的机制
Biomolecules. 2025 Apr 9;15(4):556. doi: 10.3390/biom15040556.
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The landscape of research on ferroptosis under hypoxic conditions: a bibliometric analysis.缺氧条件下铁死亡的研究概况:一项文献计量分析
Front Pharmacol. 2025 Mar 26;16:1519000. doi: 10.3389/fphar.2025.1519000. eCollection 2025.
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NINJ1 in Cell Death and Ferroptosis: Implications for Tumor Invasion and Metastasis.NINJ1在细胞死亡和铁死亡中的作用:对肿瘤侵袭和转移的影响
Cancers (Basel). 2025 Feb 26;17(5):800. doi: 10.3390/cancers17050800.
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Hypoxia induces ferroptotic cell death mediated by activation of the inner mitochondrial membrane fission protein MTP18/Drp1 in invertebrates.缺氧通过激活无脊椎动物线粒体内膜裂变蛋白MTP18/Drp1介导铁死亡性细胞死亡。
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Inhibition of GPR68 induces ferroptosis and radiosensitivity in diverse cancer cell types.抑制GPR68可诱导多种癌细胞类型发生铁死亡并增强放射敏感性。
Sci Rep. 2025 Feb 3;15(1):4074. doi: 10.1038/s41598-025-88357-x.