Role of Bim in the survival pathway induced by Raf in epithelial cells

被引:95
作者
Marani, M
Hancock, D
Lopes, R
Tenev, T
Downward, J
Lemoine, NR
机构
[1] Hammersmith Hosp, Imperial Coll London, Canc Res UK Mol Oncol Unit, London W12 0NN, England
[2] Canc Res UK London Res Inst, Signal Transduct Lab, London WC2A 3PX, England
[3] Inst Canc Res, Chester Beatty Labs, Breakthrough Toby Robins Breast Canc Res Ctr, London SW3 6JB, England
关键词
Bim; anoikis; phosphorylation; EGF receptor;
D O I
10.1038/sj.onc.1207364
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
Selective and sustained activation of the Raf/MAP kinase pathway in MCF-10A DeltaRaf-ER cells, a spontaneously immortalized human mammary epithelial cell line, was previously shown to protect these cells from suspension-induced cell death, a critical feature of the Ras-transformed phenotype. Although autocrine signalling through the EGF receptor is crucial for the protection induced by Raf in these cells, we report here the existence of an additional, more direct survival mechanism, linking Raf activation to the inhibition of a proapoptotic member of the Bcl-2 family, Bim. While detachment from the matrix results in transcriptional induction of two variants of this BH3-only protein, BimEL and BimL, activation of the Raf/ERK signalling both prevents Bim upregulation specifically and leads to phosphorylation and degradation of the BimEL isoform. This represents an important route to protect epithelial cells from the proapoptotic effect of Bim.
引用
收藏
页码:2431 / 2441
页数:11
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