Discovery of selective glucocorticoid receptor modulators by multiplexed reporter screening

被引:23
作者
Gerber, Anthony N. [1 ,2 ]
Masuno, Kiriko [1 ]
Diamond, Marc I. [3 ,4 ]
机构
[1] Univ Calif San Francisco, Dept Med, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Cardiovasc Res Inst, San Francisco, CA 94143 USA
[3] Univ Calif San Francisco, Dept Neurol, San Francisco, CA 94143 USA
[4] Univ Calif San Francisco, Dept Cellular & Mol Pharmacol, San Francisco, CA 94143 USA
基金
美国国家卫生研究院;
关键词
fluorescent protein; high-throughput screen; inhibitor; selective modulator; combinatorial therapy; EPITHELIAL SODIUM-CHANNEL; FLUORESCENT PROTEINS; ALPHA-SUBUNIT; GENE; TRANSCRIPTION; ASSAYS; CELLS; EXPRESSION; ACTIVATION; MECHANISMS;
D O I
10.1073/pnas.0812308106
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Glucocorticoids are widely used to suppress inflammation and treat various immune-mediated diseases. Some glucocorticoid receptor (GR)-regulated genes mediate the therapeutic response, whereas others cause debilitating side effects. To discover selective modulators of the GR response, we developed a high-throughput, multiplexed system to monitor regulation of 4 promoters simultaneously. An initial screen of 1,040 natural products and Food and Drug Administration-approved drugs identified modulators that caused GR to regulate only a subset of its target promoters. Some compounds selectively inhibited GR-mediated gene activation without altering the repression of cytokine expression by GR. This approach will facilitate identification of genes and small molecules that augment beneficial effects of GR and diminish deleterious ones. Our results have important implications for the development of GR modulators and the identification of cross-talk pathways that control selective GR gene regulation.
引用
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页码:4929 / 4934
页数:6
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