Ras oncogenes and their downstream targets

被引:335
作者
Rajalingam, Krishnaraj [1 ]
Schreck, Ralf [1 ]
Rapp, Ulf R. [1 ]
Albert, Stefan [1 ]
机构
[1] Univ Wurzburg, Inst Med Strahlenkunde & Zellforsch, D-97078 Wurzburg, Germany
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH | 2007年 / 1773卷 / 08期
关键词
RAS; small GTPases; RAS effector pathways; mitogenic cascade; oncogenic signaling; mutational activation; GTPASE-ACTIVATING PROTEIN; EMBRYONIC FIBROBLAST CELLS; FACIO-CUTANEOUS SYNDROME; PHOSPHOLIPASE-C-EPSILON; HRAS MUTATION ANALYSIS; TUMOR-SUPPRESSOR GENE; K-RAS; GROWTH-FACTOR; H-RAS; PHOSPHOINOSITIDE; 3-KINASE;
D O I
10.1016/j.bbamcr.2007.01.012
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
RAS proteins are small GTPases, which serve as master regulators of a myriad of signaling cascades involved in highly diverse cellular processes. RAS oncogenes have been originally discovered as retroviral oncogenes, and ever since constitutively activating RAS mutations have been identified in human tumors, they are in the focus of intense research. In this review, we summarize the biochemical properties of RAS proteins, trace down the evolution of RAS signaling and present an overview of the spatio-temporal activation of major RAS isoforms. We further discuss RAS effector pathways, their role in normal and transformed cell physiology and summarize ongoing attempts to interfere with aberrant RAS signaling. Finally, we comment on the role of micro RNAs in modulating RAS expression, contribution of RAS to stein cell function and on high-throughput analyses of RAS signaling networks. (C) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:1177 / 1195
页数:19
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