Function of the c-Myc oncogenic transcription factor

被引:325
作者
Dang, CV [1 ]
Resar, LMS
Emison, E
Kim, S
Li, Q
Prescott, JE
Wonsey, D
Zeller, K
机构
[1] Johns Hopkins Univ, Sch Med, Dept Med, Baltimore, MD 21205 USA
[2] Johns Hopkins Univ, Sch Med, Dept Pediat, Baltimore, MD 21205 USA
基金
美国国家卫生研究院;
关键词
oncogene; transcription factor; c-Myc; cell cycle; metabolism; cell adhesion; apoptosis; immortalization;
D O I
10.1006/excr.1999.4686
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The c-myc gene and the expression of the c-Myc protein are frequently altered in human cancers. The c-myc gene encodes the transcription factor c-Myc, which heterodimerizes with a partner protein, termed Max, to regulate gene expression. Max also heterodimerizes with the Mad family of proteins to repress transcription, antagonize c-Myc, and promote cellular differentiation The constitutive activation of c-myc expression is key to the genesis of many cancers, and hence the understanding of c-Myc function depends on our understanding of its target genes. In this review, we attempt to place the putative target genes of c-Myc in the context of c-Myc-mediated phenotypes. From this perspective, c-Myc emerges as an oncogenic transcription factor that integrates the cell cycle machinery with cell adhesion, cellular metabolism, and the apoptotic pathways. (C) 1999 Academic Press.
引用
收藏
页码:63 / 77
页数:15
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