ERK and cell death: mechanisms of ERK‐induced cell death–apoptosis, autophagy and senescence

S Cagnol, JC Chambard - The FEBS journal, 2010 - Wiley Online Library
S Cagnol, JC Chambard
The FEBS journal, 2010Wiley Online Library
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 …
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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