Organelle-specific regulation of ferroptosis

被引:0
作者
Xin Chen
Rui Kang
Guido Kroemer
Daolin Tang
机构
[1] Guangzhou Municipal and Guangdong Provincial Key Laboratory of Protein Modification and Degradation,Department of Surgery
[2] The Third Affiliated Hospital,undefined
[3] School of Basic Medical Sciences,undefined
[4] Guangzhou Medical University,undefined
[5] Affiliated Cancer Hospital & Institute of Guangzhou Medical University,undefined
[6] UT Southwestern Medical Center,undefined
[7] Centre de Recherche des Cordeliers,undefined
[8] Equipe labellisée par la Ligue contre le cancer,undefined
[9] Université de Paris,undefined
[10] Sorbonne Université,undefined
[11] INSERM U1138,undefined
[12] Institut Universitaire de France,undefined
[13] Metabolomics and Cell Biology Platforms,undefined
[14] Gustave Roussy Cancer Campus,undefined
[15] Pôle de Biologie,undefined
[16] Hôpital Européen Georges Pompidou,undefined
[17] AP-HP,undefined
来源
Cell Death & Differentiation | 2021年 / 28卷
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学科分类号
摘要
Ferroptosis, a cell death modality characterized by iron-dependent lipid peroxidation, is involved in the development of multiple pathological conditions, including ischemic tissue damage, infection, neurodegeneration, and cancer. The cellular machinery responsible for the execution of ferroptosis integrates multiple pro-survival or pro-death signals from subcellular organelles and then ‘decides’ whether to engage the lethal process or not. Here, we outline the evidence implicating different organelles (including mitochondria, lysosomes, endoplasmic reticulum, lipid droplets, peroxisomes, Golgi apparatus, and nucleus) in the ignition or avoidance of ferroptosis, while emphasizing their potential relevance for human disease and their targetability for pharmacological interventions.
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页码:2843 / 2856
页数:13
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