PI3K: A Crucial Piece in the RAS Signaling Puzzle

被引:39
|
作者
Krygowska, Agata Adelajda [1 ]
Castellano, Esther [1 ]
机构
[1] Queen Mary Univ London, Ctr Canc & Inflammat, Barts Canc Inst, London EC13 6BQ, England
来源
关键词
PHOSPHOINOSITIDE 3-KINASE P110-ALPHA; EXTRACELLULAR-MATRIX SYNTHESIS; MUTANT COLORECTAL CANCERS; CELL LUNG-CANCER; G-BETA-GAMMA; PHOSPHATIDYLINOSITOL; 3-KINASE; K-RAS; ANTITUMOR-ACTIVITY; ONCOGENIC RAS; CROSS-TALK;
D O I
10.1101/cshperspect.a031450
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
RAS proteins are key signaling switches essential for control of proliferation, differentiation, and survival of eukaryotic cells. RAS proteins are mutated in 30% of human cancers. In addition, mutations in upstream or downstream signaling components also contribute to oncogenic activation of the pathway. RAS proteins exert their functions through activation of several signaling pathways and dissecting the contributions of these effectors in normal cells and in cancer is an ongoing challenge. In this review, we summarize our current knowledge about how RAS regulates type I phosphatidylinositol 3-kinase (PI3K), one of the main RAS effectors. RAS signaling through PI3K is necessary for normal lymphatic vasculature development and for RAS-induced transformation in vitro and in vivo, especially in lung cancer, where it is essential for tumor initiation and necessary for tumor maintenance.
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页数:19
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