Oncogenes and Tumor Suppressor Genes

被引:259
|
作者
Lee, Eva Y. H. P. [2 ,3 ]
Muller, William J. [1 ]
机构
[1] McGill Univ, Goodman Canc Ctr, Montreal, PQ H3A 1A3, Canada
[2] Univ Calif Irvine, Dept Biol Chem, Irvine, CA 92697 USA
[3] Univ Calif Irvine, Dept Dev & Cell Biol, Irvine, CA 92697 USA
来源
关键词
HUMAN-BREAST-CANCER; EPIDERMAL-GROWTH-FACTOR; FOCAL ADHESION KINASE; MAMMARY EPITHELIAL-CELLS; TRANSGENIC-MOUSE MODEL; SRC TYROSINE KINASE; PLAY DISTINCT ROLES; SUSCEPTIBILITY GENE; NEU PROTOONCOGENE; C-SRC;
D O I
10.1101/cshperspect.a003236
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Breast cancer progression involves multiple genetic events, which can activate dominant-acting oncogenes and disrupt the function of specific tumor suppressor genes. This article describes several key oncogene and tumor suppressor signaling networks that have been implicated in breast cancer progression. Among the tumor suppressors, the article emphasizes BRCA1/2 and p53 tumor suppressors. In addition to these well characterized tumor suppressors, the article highlights the importance of PTEN tumor suppressor in counteracting PI3K signaling from activated oncogenes such as ErbB2. This article discusses the use of mouse models of human breast that recapitulate the key genetic events involved in the initiation and progression of breast cancer. Finally, the therapeutic potential of targeting these key tumor suppressor and oncogene signaling networks is discussed.
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页数:18
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