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线粒体介导的疾病治疗中的铁死亡:从分子机制到意义。

Mitochondria-mediated Ferroptosis in Diseases Therapy: From Molecular Mechanisms to Implications.

机构信息

The First Clinical College, Guangdong Medical University, Zhanjiang, Guangdong, China.

Beijing Hospital of Traditional Chinese Medicine, Capital Medical University, Beijing, China.

出版信息

Aging Dis. 2024 Apr 1;15(2):714-738. doi: 10.14336/AD.2023.0717.

DOI:10.14336/AD.2023.0717
PMID:37548939
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10917537/
Abstract

Ferroptosis, a type of cell death involving iron and lipid peroxidation, has been found to be closely associated with the development of many diseases. Mitochondria are vital components of eukaryotic cells, serving important functions in energy production, cellular metabolism, and apoptosis regulation. Presently, the precise relationship between mitochondria and ferroptosis remains unclear. In this study, we aim to systematically elucidate the mechanisms via which mitochondria regulate ferroptosis from multiple perspectives to provide novel insights into mitochondrial functions in ferroptosis. Additionally, we present a comprehensive overview of how mitochondria contribute to ferroptosis in different conditions, including cancer, cardiovascular disease, inflammatory disease, mitochondrial DNA depletion syndrome, and novel coronavirus pneumonia. Gaining a comprehensive understanding of the involvement of mitochondria in ferroptosis could lead to more effective approaches for both basic cell biology studies and medical treatments.

摘要

铁死亡是一种涉及铁和脂质过氧化的细胞死亡方式,与许多疾病的发生密切相关。线粒体是真核细胞的重要组成部分,在能量产生、细胞代谢和细胞凋亡调节中发挥着重要作用。目前,线粒体与铁死亡之间的确切关系尚不清楚。在这项研究中,我们旨在从多个角度系统阐明线粒体调节铁死亡的机制,为线粒体在铁死亡中的功能提供新的见解。此外,我们还全面介绍了线粒体在不同条件下(包括癌症、心血管疾病、炎症性疾病、线粒体 DNA 耗竭综合征和新型冠状病毒肺炎)如何促进铁死亡。全面了解线粒体在铁死亡中的作用可能会为基础细胞生物学研究和医学治疗提供更有效的方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92bd/10917537/b2e4c0752c76/AD-15-2-714-g3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92bd/10917537/3ca8d1047a08/AD-15-2-714-g1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92bd/10917537/18cf5c47d4ad/AD-15-2-714-g2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92bd/10917537/b2e4c0752c76/AD-15-2-714-g3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92bd/10917537/3ca8d1047a08/AD-15-2-714-g1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92bd/10917537/18cf5c47d4ad/AD-15-2-714-g2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92bd/10917537/b2e4c0752c76/AD-15-2-714-g3.jpg

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Mitochondria-localized cGAS suppresses ferroptosis to promote cancer progression.线粒体定位的 cGAS 抑制铁死亡以促进癌症进展。
Cell Res. 2023 Apr;33(4):299-311. doi: 10.1038/s41422-023-00788-1. Epub 2023 Mar 2.
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DHODH Inhibition Exerts Synergistic Therapeutic Effect with Cisplatin to Induce Ferroptosis in Cervical Cancer through Regulating mTOR Pathway.二氢乳清酸脱氢酶抑制与顺铂发挥协同治疗作用,通过调节mTOR通路诱导宫颈癌铁死亡。
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Mitochondria regulate intracellular coenzyme Q transport and ferroptotic resistance via STARD7.
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Targeting PRMT1-mediated methylation of TAF15 to protect against myocardial infarction by inhibiting ferroptosis via the GPX4/NRF2 pathway.靶向PRMT1介导的TAF15甲基化,通过GPX4/NRF2途径抑制铁死亡来预防心肌梗死。
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Tanshinone IIA Promotes Functional Recovery After Spinal Cord Injury by Inhibiting Neuron and Oligodendrocyte Ferroptosis Through the GPX4/ACSL4 Axis.丹参酮IIA通过GPX4/ACSL4轴抑制神经元和少突胶质细胞铁死亡促进脊髓损伤后的功能恢复。
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Ferroptosis in Cancer: Mechanism and Therapeutic Potential.癌症中的铁死亡:机制与治疗潜力
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Metal-dependent cell death resistance contribute to lymph node metastasis of oral squamous cell carcinoma.金属依赖性细胞死亡抗性促进口腔鳞状细胞癌的淋巴结转移。
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Cells. 2025 Feb 2;14(3):213. doi: 10.3390/cells14030213.
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线粒体通过 STARD7 调节细胞内辅酶 Q 转运和铁死亡抵抗。
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A ferroptosis defense mechanism mediated by glycerol-3-phosphate dehydrogenase 2 in mitochondria.线粒体中甘油-3-磷酸脱氢酶 2 介导的铁死亡防御机制。
Proc Natl Acad Sci U S A. 2022 Jun 28;119(26):e2121987119. doi: 10.1073/pnas.2121987119. Epub 2022 Jun 24.
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Cell death regulation by MAMs: from molecular mechanisms to therapeutic implications in cardiovascular diseases.MAMs 调控细胞死亡:从分子机制到心血管疾病的治疗意义。
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