Gerber Anthony N, Masuno Kiriko, Diamond Marc I
Department of Medicine, University of California, San Francisco, CA 94143-2280, USA.
Proc Natl Acad Sci U S A. 2009 Mar 24;106(12):4929-34. doi: 10.1073/pnas.0812308106. Epub 2009 Mar 2.
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.
糖皮质激素被广泛用于抑制炎症和治疗各种免疫介导的疾病。一些糖皮质激素受体(GR)调节的基因介导治疗反应,而其他基因则会导致使人衰弱的副作用。为了发现GR反应的选择性调节剂,我们开发了一种高通量、多重系统来同时监测4个启动子的调节。对1040种天然产物和美国食品药品监督管理局批准的药物进行的初步筛选,确定了能使GR仅调节其目标启动子子集的调节剂。一些化合物选择性地抑制GR介导的基因激活,而不改变GR对细胞因子表达的抑制作用。这种方法将有助于识别增强GR有益作用并减少有害作用的基因和小分子。我们的结果对GR调节剂的开发以及控制选择性GR基因调节的信号通路的识别具有重要意义。