ERK and cell death: Mechanisms of ERK-induced cell death - apoptosis, autophagy and senescence

被引:1057
作者
Cagnol, Sebastien [1 ]
Chambard, Jean-Claude [2 ]
机构
[1] Univ Sherbrooke, Dept Anat & Cellular Biol, Fac Med & Hlth Sci, Sherbrooke, PQ J1K 2R1, Canada
[2] Univ Nice, Inst Dev Biol & Canc, F-06108 Nice 2, France
关键词
apoptosis; autophagy; DUSP; ERK; ROS; senescence; SIGNAL-REGULATED KINASE; ACTIVATED PROTEIN-KINASE; CISPLATIN-INDUCED APOPTOSIS; RENAL EPITHELIAL-CELLS; CYTOSOLIC PHOSPHOLIPASE A(2); ONCOGENE-INDUCED SENESCENCE; LIGAND-INDUCED APOPTOSIS; TAXOL-INDUCED APOPTOSIS; TRAIL-INDUCED APOPTOSIS; PROXIMAL TUBULAR CELLS;
D O I
10.1111/j.1742-4658.2009.07366.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The Ras/Raf/extracellular signal-regulated kinase (ERK) signaling pathway plays a crucial role in almost all cell functions and therefore requires exquisite control of its spatiotemporal activity. Depending on the cell type and stimulus, ERK activity will mediate different antiproliferative events, such as apoptosis, autophagy and senescence in vitro and in vivo. ERK activity can promote either intrinsic or extrinsic apoptotic pathways by induction of mitochondrial cytochrome c release or caspase-8 activation, permanent cell cycle arrest or autophagic vacuolization. These unusual effects require sustained ERK activity in specific subcellular compartments and could depend on the presence of reactive oxygen species. We will summarize the mechanisms involved in Ras/Raf/ERK antiproliferative functions.
引用
收藏
页码:2 / 21
页数:20
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