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熊果酸抑制人乳腺上皮细胞中环氧化酶-2的转录。

Ursolic acid inhibits cyclooxygenase-2 transcription in human mammary epithelial cells.

作者信息

Subbaramaiah K, Michaluart P, Sporn M B, Dannenberg A J

机构信息

Department of Medicine, New York Presbyterian Hospital-Cornell, New York 10021, USA.

出版信息

Cancer Res. 2000 May 1;60(9):2399-404.

Abstract

We investigated the effects of ursolic acid, a chemopreventive agent, on the expression of cyclooxygenase-2 (COX-2) in phorbol 12-myristate 13-acetate (PMA)-treated human mammary and oral epithelial cells. Treatment with ursolic acid suppressed PMA-mediated induction of COX-2 protein and synthesis of prostaglandin E2. Ursolic acid also suppressed the induction of COX-2 mRNA by PMA. Nuclear run-offs revealed increased rates of COX-2 transcription after treatment with PMA, an effect that was inhibited by ursolic acid. Transient transfections indicated that the effects of PMA were mediated by a cyclic AMP response element in the COX-2 promoter. Ursolic acid inhibited PMA-mediated activation of protein kinase C, extracellular signal-regulated kinase 1/2, c-Jun N-terminal kinase, and p38 mitogen-activated protein kinases. Treatment with PMA increased activator protein-1 activity and the binding of c-Jun to the cyclic AMP response element of the COX-2 promoter, effects that were blocked by ursolic acid. These data are important for understanding the anticancer and anti-inflammatory properties of ursolic acid.

摘要

我们研究了化学预防剂熊果酸对佛波酯12-肉豆蔻酸酯13-乙酸酯(PMA)处理的人乳腺和口腔上皮细胞中环氧合酶-2(COX-2)表达的影响。用熊果酸处理可抑制PMA介导的COX-2蛋白诱导和前列腺素E2的合成。熊果酸还可抑制PMA诱导的COX-2 mRNA。细胞核转录分析显示,PMA处理后COX-2转录速率增加,而熊果酸可抑制这一效应。瞬时转染表明,PMA的作用是由COX-2启动子中的环磷酸腺苷反应元件介导的。熊果酸可抑制PMA介导的蛋白激酶C、细胞外信号调节激酶1/2、c-Jun氨基末端激酶和p38丝裂原活化蛋白激酶的激活。PMA处理可增加活化蛋白-1活性以及c-Jun与COX-2启动子环磷酸腺苷反应元件的结合,而这些效应均被熊果酸阻断。这些数据对于理解熊果酸的抗癌和抗炎特性具有重要意义。

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