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铁死亡的特征与生物标志物

Characteristics and Biomarkers of Ferroptosis.

作者信息

Chen Xin, Comish Paul B, Tang Daolin, Kang Rui

机构信息

Guangzhou Municipal and Guangdong Provincial Key Laboratory of Protein Modification and Degradation, The Third Affiliated Hospital, School of Basic Medical Sciences, Guangzhou Medical University, Guangzhou, China.

Affiliated Cancer Hospital & Institute of Guangzhou Medical University, Guangzhou, China.

出版信息

Front Cell Dev Biol. 2021 Jan 21;9:637162. doi: 10.3389/fcell.2021.637162. eCollection 2021.

DOI:10.3389/fcell.2021.637162
PMID:33553189
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7859349/
Abstract

The induction and consequences of regulated cell death (RCD) are accompanied by changes in gene and protein expression, biochemical pathways, as well as cell morphology and size. Such RCDs have a significant impact on development, tissue homeostasis, and the occurrence and progression of disease. Among different forms of RCD, ferroptosis appears to be the main cause of tissue damage driven by iron overload and lipid peroxidation. In fact, the dysfunctional ferroptotic response is implicated in a variety of pathological conditions and diseases, such as neurodegenerative diseases, tissue ischemia-reperfusion injury, tumorigenesis, infections, and immune diseases. Ferroptotic response can be fine-tuned through various oxidative stress and antioxidant defense pathways, coupling with metabolism, gene transcription, and protein degradation machinery. Accordingly, a series of ferroptosis inducers or inhibitors targeting redox- or iron metabolism-related proteins or signal transduction have been developed. Although this kind of RCD has recently attracted great interest in basic and clinical research, detecting and monitoring a ferroptotic response still faces challenges. In this mini-review, we not only summarize the latest knowledge about the characteristics of ferroptosis and , but also discuss the specificity and limitations of current biomarkers of ferroptosis.

摘要

程序性细胞死亡(RCD)的诱导及其后果伴随着基因和蛋白质表达、生化途径以及细胞形态和大小的变化。此类程序性细胞死亡对发育、组织稳态以及疾病的发生和发展具有重大影响。在不同形式的程序性细胞死亡中,铁死亡似乎是铁过载和脂质过氧化驱动的组织损伤的主要原因。事实上,功能失调的铁死亡反应与多种病理状况和疾病有关,如神经退行性疾病、组织缺血再灌注损伤、肿瘤发生、感染和免疫疾病。铁死亡反应可通过各种氧化应激和抗氧化防御途径进行微调,并与代谢、基因转录和蛋白质降解机制相互关联。因此,已经开发出一系列针对氧化还原或铁代谢相关蛋白或信号转导的铁死亡诱导剂或抑制剂。尽管这种程序性细胞死亡最近在基础和临床研究中引起了极大关注,但检测和监测铁死亡反应仍然面临挑战。在本综述中,我们不仅总结了关于铁死亡特征 的最新知识,还讨论了当前铁死亡生物标志物的特异性和局限性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e0d/7859349/fd062e13d4fa/fcell-09-637162-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e0d/7859349/fd062e13d4fa/fcell-09-637162-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e0d/7859349/fd062e13d4fa/fcell-09-637162-g001.jpg

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Characteristics and Biomarkers of Ferroptosis.铁死亡的特征与生物标志物
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2
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Biol Trace Elem Res. 2025 Sep 8. doi: 10.1007/s12011-025-04818-4.
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The novel role of DUSP4 in suppressing ferroptosis and promoting cytotoxicity of CD8 T cells in MSI colorectal cancer.双特异性磷酸酶4(DUSP4)在微卫星高度不稳定(MSI)结直肠癌中抑制铁死亡及促进CD8 T细胞细胞毒性方面的新作用
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本文引用的文献

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Broadening horizons: the role of ferroptosis in cancer.拓宽视野:铁死亡在癌症中的作用。
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Ferroptotic damage promotes pancreatic tumorigenesis through a TMEM173/STING-dependent DNA sensor pathway.铁死亡损伤通过依赖TMEM173/STING的DNA传感途径促进胰腺肿瘤发生。
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Ferroptosis: molecular mechanisms and health implications.铁死亡:分子机制与健康关联。
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Comparative proteomics of HepG2 cells reveals NGLY1 as an important regulator of ferroptosis resistance and iron uptake.HepG2细胞的比较蛋白质组学揭示NGLY1是铁死亡抗性和铁摄取的重要调节因子。
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Synergistic effect of regorafenib with aminoglycosides in ferroptosis-mediated liver injury.瑞戈非尼与氨基糖苷类药物在铁死亡介导的肝损伤中的协同作用。
Front Pharmacol. 2025 Jul 15;16:1586578. doi: 10.3389/fphar.2025.1586578. eCollection 2025.
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Role of Ferroptosis in Alveolar Epithelial Cells in Acute Respiratory Distress Syndrome.铁死亡在急性呼吸窘迫综合征肺泡上皮细胞中的作用
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Dietary Cottonseed Protein Substituting Fish Meal Induces Hepatic Ferroptosis Through SIRT1-YAP-TRFC Axis in : Implications for Inflammatory Regulation and Liver Health.膳食棉籽蛋白替代鱼粉通过SIRT1-YAP-TRFC轴诱导肝铁死亡:对炎症调节和肝脏健康的影响
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Bardoxolone methyl inhibits ferroptosis through the Keap1‑Nrf2 pathway in renal tubular epithelial cells.巴多昔芬甲酯通过Keap1-Nrf2途径抑制肾小管上皮细胞的铁死亡。
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Ferroptosis.铁死亡。
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3D Culture Models with CRISPR Screens Reveal Hyperactive NRF2 as a Prerequisite for Spheroid Formation via Regulation of Proliferation and Ferroptosis.CRISPR 筛选的 3D 培养模型揭示了 NRF2 的过度激活是通过调节增殖和铁死亡来形成球体的前提条件。
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Iron Metabolism in Ferroptosis.铁死亡中的铁代谢
Front Cell Dev Biol. 2020 Oct 7;8:590226. doi: 10.3389/fcell.2020.590226. eCollection 2020.
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Oxidative Damage and Antioxidant Defense in Ferroptosis.铁死亡中的氧化损伤与抗氧化防御
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LncRNA PVT1 regulates ferroptosis through miR-214-mediated TFR1 and p53.长链非编码 RNA PVT1 通过 miR-214 介导的 TFR1 和 p53 调控铁死亡。
Life Sci. 2020 Nov 1;260:118305. doi: 10.1016/j.lfs.2020.118305. Epub 2020 Aug 20.
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NEDD4L-mediated LTF protein degradation limits ferroptosis.NEDD4L 介导的 LTF 蛋白降解限制铁死亡。
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