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铁死亡:一种依赖铁的细胞死亡形式,与代谢、疾病、免疫细胞和靶向治疗有关。

Ferroptosis: an iron-dependent cell death form linking metabolism, diseases, immune cell and targeted therapy.

机构信息

National Center for International Research of Bio-Targeting Theranostics, Guangxi Key Laboratory of Bio-Targeting Theranostics, Collaborative Innovation Center for Targeting Tumor Diagnosis and Therapy, Guangxi Talent Highland of Bio-Targeting Theranostics, Guangxi Medical University, Nanning, 530021, Guangxi, China.

出版信息

Clin Transl Oncol. 2022 Jan;24(1):1-12. doi: 10.1007/s12094-021-02669-8. Epub 2021 Jun 23.

DOI:10.1007/s12094-021-02669-8
PMID:34160772
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8220428/
Abstract

Compared with the traditional forms of cell death-apoptosis, necrosis and autophagy, ferroptosis is a novel form of iron-dependent programmed cell death forms which is different from the above traditional forms of cell death. Brent R Stockwell, a Professor of Columbia University, firstly proposed that this from of cell death was named ferroptosis in 2012. The main characteristics of ferroptosis is increasing iron loading and driving a lot of lipid peroxide generated and ultimately lead to cell death. In this paper, the mechanism of ferroptosis, relationship between ferroptosis and common diseases and immune state of body are reviewed, and the inhibitors and inducers related to ferroptosis that have been found are summarized to provide medicine exploration targeted of ferroptosis and reference for the research in the future.

摘要

与传统的细胞死亡形式——凋亡、坏死和自噬相比,铁死亡是一种新型的铁依赖性程序性细胞死亡形式,与上述传统的细胞死亡形式不同。2012 年,哥伦比亚大学教授布伦特·R·斯托克韦尔首次提出将这种细胞死亡形式命名为铁死亡。铁死亡的主要特征是增加铁的负载并驱动大量脂质过氧化物的产生,最终导致细胞死亡。本文综述了铁死亡的机制、铁死亡与常见疾病和机体免疫状态的关系,总结了已发现的与铁死亡相关的抑制剂和诱导剂,为铁死亡的药物探索提供靶点,为未来的研究提供参考。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9558/8220428/992eecf85a0e/12094_2021_2669_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9558/8220428/bacbf3548049/12094_2021_2669_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9558/8220428/7d4f26af2277/12094_2021_2669_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9558/8220428/c7455fe2cf1b/12094_2021_2669_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9558/8220428/e2d87efadc77/12094_2021_2669_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9558/8220428/aa597a5c44e4/12094_2021_2669_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9558/8220428/992eecf85a0e/12094_2021_2669_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9558/8220428/bacbf3548049/12094_2021_2669_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9558/8220428/7d4f26af2277/12094_2021_2669_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9558/8220428/c7455fe2cf1b/12094_2021_2669_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9558/8220428/e2d87efadc77/12094_2021_2669_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9558/8220428/aa597a5c44e4/12094_2021_2669_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9558/8220428/992eecf85a0e/12094_2021_2669_Fig6_HTML.jpg

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Adv Sci (Weinh). 2021 Mar 8;8(10):2004680. doi: 10.1002/advs.202004680. eCollection 2021 May.
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Oxygenated phosphatidylethanolamine navigates phagocytosis of ferroptotic cells by interacting with TLR2.氧合磷脂酰乙醇胺通过与 TLR2 相互作用来引导铁死亡细胞的吞噬作用。
Cell Death Differ. 2021 Jun;28(6):1971-1989. doi: 10.1038/s41418-020-00719-2. Epub 2021 Jan 11.
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Loss of ferroportin induces memory impairment by promoting ferroptosis in Alzheimer's disease.
Front Neurosci. 2025 May 12;19:1591417. doi: 10.3389/fnins.2025.1591417. eCollection 2025.
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The m6A methyltransferase METTL3 affects ferroptosis in non-small cell lung cancer by regulating the PTEN/PI3K/AKT pathway.m6A甲基转移酶METTL3通过调节PTEN/PI3K/AKT信号通路影响非小细胞肺癌中的铁死亡。
Discov Oncol. 2025 Apr 18;16(1):559. doi: 10.1007/s12672-025-02330-8.
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Disulfidptosis: a novel gene-based signature predicts prognosis and immunotherapy efficacy of pancreatic adenocarcinoma.二硫化物诱导的细胞焦亡:一种基于新基因的特征可预测胰腺腺癌的预后和免疫治疗疗效。
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Polydatin and Nicotinamide Prevent Iron Accumulation and Lipid Peroxidation in Cellular Models of Mitochondrial Diseases.虎杖苷和烟酰胺可预防线粒体疾病细胞模型中的铁积累和脂质过氧化。
Antioxidants (Basel). 2025 Feb 13;14(2):215. doi: 10.3390/antiox14020215.
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Antioxidants (Basel). 2025 Jan 24;14(2):137. doi: 10.3390/antiox14020137.
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