Nuclear Receptor Coregulators in Cancer Biology

被引:98
作者
O'Malley, Bert W. [1 ]
Kumar, Rakesh [2 ,3 ]
机构
[1] Baylor Coll Med, Dept Mol & Cellular Biol, Houston, TX 77030 USA
[2] George Washington Univ, Med Ctr, Dept Biochem & Mol Biol, Washington, DC 20037 USA
[3] George Washington Univ, Med Ctr, Inst Coregulator Biol, Washington, DC 20037 USA
基金
美国国家卫生研究院;
关键词
METASTASIS-ASSOCIATED PROTEIN-1; ESTROGEN-RECEPTOR; BREAST-CANCER; STEROID-RECEPTOR; TRANSCRIPTIONAL ACTIVITY; TAMOXIFEN RESISTANCE; GENE AMPLIFICATION; COACTIVATOR; IDENTIFICATION; ACTIVATION;
D O I
10.1158/0008-5472.CAN-09-2223
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Coregulators (coactivators and corepressors) occupy the driving seat for actions of all nuclear receptors, and consequently, selective receptor modulator drugs. The potency and selectivity for subreactions of transcription reside in the coactivators, and thus, they are critically important for tissue-selective gene function. Each tissue has a "quantitative finger print" of coactivators based on its relative inherited concentrations of these molecules. When the cellular concentration of a coactivator is altered, genetic dysfunction usually leads to a pathologic outcome. For example, many cancers overexpress "growth coactivators." In this way, the cancer cell can hijack these coactivator molecules to drive proliferation and metastasis. The present review contains summaries of selective coactivators and corepressors that have been demonstrated to play important roles in the malignant process and emphasizes their importance for future therapeutic interventions. [Cancer Res 2009;69(21):8217-22]
引用
收藏
页码:8217 / 8222
页数:6
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