Sos-mediated cross-activation of wild-type Ras by oncogenic Ras is essential for tumorigenesis

被引:132
作者
Jeng, Hao-Hsuan [1 ,2 ]
Taylor, Laura J. [1 ]
Bar-Sagi, Dafna [1 ]
机构
[1] NYU, Sch Med, Dept Biochem & Mol Pharmacol, New York, NY 10016 USA
[2] NYU, Sch Med, Cell & Mol Biol Training Program, New York, NY 10016 USA
来源
NATURE COMMUNICATIONS | 2012年 / 3卷
基金
美国国家卫生研究院;
关键词
GUANINE-NUCLEOTIDE EXCHANGE; GROWTH-FACTOR-ALPHA; DISTINCT FUNCTIONS; RECEPTOR; GRB2; CANCER; PHOSPHORYLATION; TRANSFORMATION; EXPRESSION; HOMOLOGS;
D O I
10.1038/ncomms2173
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Mammalian cells contain three closely related ras genes, H-ras, K-ras and N-ras. Although in a given tumour type, oncogenic mutations are selectively observed in only one of the ras genes, the acquisition of the transformed phenotype has been shown to require the contribution of the normal products of the other ras genes. Here we demonstrate that oncogenic K-Ras promotes the activation of wild-type H-and N-Ras. This activation is mediated by oncogenic K-Ras-dependent allosteric stimulation of Sos and confers a growth advantage to oncogenic K-Ras harbouring cancer cells. These findings underscore the complementary functions of oncogenic and wild-type Ras in tumour cells and identify a potential new targeting strategy for Ras-driven tumours.
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收藏
页数:8
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