Schulze A, Lehmann K, Jefferies H B, McMahon M, Downward J
Signal Transduction Laboratory, Imperial Cancer Research Fund, London WC2A 3PX, UK.
Genes Dev. 2001 Apr 15;15(8):981-94. doi: 10.1101/gad.191101.
Activation of the Raf/MAP kinase pathway is a critical event in tumorigenesis induced by RAS and other oncogenes, a major role of this signaling system being the regulation of cellular transcription factors. To address the contribution of MAP kinase mediated transcriptional changes to the transformed phenotype, we used an inducible form of Raf to analyze early changes in the transcription of some 6000 genes following activation of the kinase in a normal human breast epithelial cell line. Of the more than 120 significant changes in mRNA level detected, genes promoting cell proliferation, invasiveness, and angiogenesis featured prominently. Some of the most strongly induced genes encoded growth factors of the EGF family: Autocrine activation of the EGF receptor was shown to be responsible for the ability of Raf activation to protect these cells from apoptosis induced by detachment of cells from extracellular matrix (anoikis), which is a critical component of the transformed phenotype.
Raf/丝裂原活化蛋白激酶(MAP激酶)信号通路的激活是由RAS及其他致癌基因诱导的肿瘤发生过程中的关键事件,该信号系统的一个主要作用是调节细胞转录因子。为了探究MAP激酶介导的转录变化对转化表型的作用,我们使用了一种可诱导形式的Raf,来分析在正常人乳腺上皮细胞系中激酶激活后约6000个基因转录的早期变化。在检测到的120多个显著的mRNA水平变化中,促进细胞增殖、侵袭和血管生成的基因尤为突出。一些诱导最强的基因编码表皮生长因子(EGF)家族的生长因子:EGF受体的自分泌激活被证明是Raf激活使这些细胞免受因细胞与细胞外基质脱离(失巢凋亡)所诱导的凋亡的原因,而失巢凋亡是转化表型的一个关键组成部分。