Wu Kenneth K
Vascular Biology Research Center and Division of Hematology, Department of Medicine, The University of Texas Health Science Center at Houston, Texas 77030, USA.
Thromb Haemost. 2006 Oct;96(4):417-22.
Potent selective cyclooxygenase-2 (COX-2) inhibitors are effective in controlling inflammatory disorders but are associated with cardiovascular complications. Their clinical use has been severely limited. We propose that transcription-based inhibition of COX-2 expression represents a therapeutic strategy that may circumvent the undesired complications of COX-2 inhibitors. Reported data from several laboratories including ours have identified C/EBPbeta as a key transactivator mediating COX-2 transcriptional activation induced by diverse pro-inflammatory mediators. Results from our recent work show that sodium salicylate at pharmacological concentrations inhibits C/EBPbeta binding to COX-2 promoter by direct inhibition of p90 ribosomal S6 kinase (RSK). RSK phosphorylates C/EBPbeta and stimulates its binding to enhancer elements. We propose that RSK1/2 is a potential target for screening drugs with novel anti-inflammatory and anti-neoplastic therapeutic potentials.
强效选择性环氧化酶-2(COX-2)抑制剂在控制炎症性疾病方面有效,但与心血管并发症相关。它们的临床应用受到严重限制。我们提出,基于转录的COX-2表达抑制代表了一种治疗策略,可能规避COX-2抑制剂的不良并发症。包括我们实验室在内的几个实验室报告的数据已确定C/EBPβ是介导多种促炎介质诱导的COX-2转录激活的关键反式激活因子。我们最近的研究结果表明,药理浓度的水杨酸钠通过直接抑制p90核糖体S6激酶(RSK)来抑制C/EBPβ与COX-2启动子的结合。RSK使C/EBPβ磷酸化并刺激其与增强子元件的结合。我们提出,RSK1/2是筛选具有新型抗炎和抗肿瘤治疗潜力药物的潜在靶点。