Proteolytic Control of the Oncoprotein Transcription Factor Myc

被引:87
作者
Thomas, Lance R. [1 ]
Tansey, William P. [1 ]
机构
[1] Vanderbilt Univ, Sch Med, Dept Cell & Dev Biol, Nashville, TN 37212 USA
来源
ADVANCES IN CANCER RESEARCH, VOL 110 | 2011年 / 110卷
关键词
PROTEASOME-MEDIATED DEGRADATION; FBW7 UBIQUITIN LIGASE; REGULATES C-MYC; PROTEIN STABILITY; IN-VIVO; DEPENDENT PROTEOLYSIS; HUMAN-CELLS; MULTISITE PHOSPHORYLATION; MESSENGER-RNA; DNA-BINDING;
D O I
10.1016/B978-0-12-386469-7.00004-9
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The c-Myc oncogene encodes a multifunctional transcription factor that directs the expression of genes required for cell growth and proliferation. Consistent with its potent growth-promoting properties, cells have evolved numerous mechanisms that limit the expression and activity of Myc. One of the most prominent of these mechanisms is proteolysis, which destroys Myc within minutes of its synthesis. The rapid and controlled destruction of Myc keeps its levels low and precisely tied to processes that regulate Myc production. In this review, we discuss how Myc protein stability is regulated and the influence of Myc proteolysis on its function. We describe what is known about how Myc is destroyed by ubiquitin (Ub)-mediaied proteolysis, attempt to rationalize the role of different Ub-protein ligases and deubiquitylating enzymes (dUbs) in the regulation of Myc stability, and detail how these processes go awry in cancer. Finally, we discuss how our understanding of Myc regulation by the ubiquitin-proteasome system (UPS) can expose strategies for therapeutic intervention in human malignancies. (C) 2011 Elsevier Inc.
引用
收藏
页码:77 / 106
页数:30
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