共 242 条
Function of the c-Myc oncogenic transcription factor
被引:325
作者:

Dang, CV
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机构:
Johns Hopkins Univ, Sch Med, Dept Med, Baltimore, MD 21205 USA Johns Hopkins Univ, Sch Med, Dept Med, Baltimore, MD 21205 USA

Resar, LMS
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机构: Johns Hopkins Univ, Sch Med, Dept Med, Baltimore, MD 21205 USA

Emison, E
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机构: Johns Hopkins Univ, Sch Med, Dept Med, Baltimore, MD 21205 USA

Kim, S
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机构: Johns Hopkins Univ, Sch Med, Dept Med, Baltimore, MD 21205 USA

Li, Q
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机构: Johns Hopkins Univ, Sch Med, Dept Med, Baltimore, MD 21205 USA

Prescott, JE
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机构: Johns Hopkins Univ, Sch Med, Dept Med, Baltimore, MD 21205 USA

Wonsey, D
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机构: Johns Hopkins Univ, Sch Med, Dept Med, Baltimore, MD 21205 USA

Zeller, K
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机构: Johns Hopkins Univ, Sch Med, Dept Med, Baltimore, MD 21205 USA
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.
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页码:63 / 77
页数:15
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