MINIREVIEW
ERK and cell death: Mechanisms of ERK-induced cell death – apoptosis, autophagy and senescence
Article first published online: 16 OCT 2009
DOI: 10.1111/j.1742-4658.2009.07366.x
© 2009 The Authors Journal compilation © 2009 FEBS
Additional Information
How to Cite
Cagnol, S. and Chambard, J.-C. (2010), ERK and cell death: Mechanisms of ERK-induced cell death – apoptosis, autophagy and senescence. FEBS Journal, 277: 2–21. doi: 10.1111/j.1742-4658.2009.07366.x
Publication History
- Issue published online: 15 DEC 2009
- Article first published online: 16 OCT 2009
- (Received 18 June 2009, revised 26 August 2009, accepted 9 September 2009)
- Abstract
- Article
- References
- Cited By
Keywords:
- apoptosis;
- autophagy;
- DUSP;
- ERK;
- ROS;
- senescence
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.

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