粒体自噬
帕金
自噬
品脱1
泛素连接酶
癌细胞
线粒体
泛素
细胞生物学
生物
癌症
癌症研究
细胞凋亡
遗传学
医学
基因
病理
疾病
帕金森病
作者
Elodie Villa,Emma Proïcs,Camila Rubio‐Patiño,Sandrine Obba,Barbara Zunino,Jozef P. Bossowski,R. Rozier,Johanna Chiche,Laura Mondragón,Joel S. Riley,Sandrine Marchetti,Els Verhoeyen,Stephen W. G. Tait,Jean‐Ehrland Ricci
出处
期刊:Cell Reports
[Elsevier]
日期:2017-09-01
卷期号:20 (12): 2846-2859
被引量:247
标识
DOI:10.1016/j.celrep.2017.08.087
摘要
Mitophagy is an evolutionarily conserved process that selectively targets impaired mitochondria for degradation. Defects in mitophagy are often associated with diverse pathologies, including cancer. Because the main known regulators of mitophagy are frequently inactivated in cancer cells, the mechanisms that regulate mitophagy in cancer cells are not fully understood. Here, we identified an E3 ubiquitin ligase (ARIH1/HHARI) that triggers mitophagy in cancer cells in a PINK1-dependent manner. We found that ARIH1/HHARI polyubiquitinates damaged mitochondria, leading to their removal via autophagy. Importantly, ARIH1 is widely expressed in cancer cells, notably in breast and lung adenocarcinomas; ARIH1 expression protects against chemotherapy-induced death. These data challenge the view that the main regulators of mitophagy are tumor suppressors, arguing instead that ARIH1-mediated mitophagy promotes therapeutic resistance.
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