Subbaramaiah Kotha, Cole Philip A, Dannenberg Andrew J
Department of Medicine, New York Presbyterian Hospital-Cornell and Strang Cancer Prevention Center, New York, New York 10021, USA.
Cancer Res. 2002 May 1;62(9):2522-30.
Treatment with retinoic acid (RA) or carnosol, two structurally unrelated compounds with anticancer properties, inhibited phorbol ester (PMA)-mediated induction of activator protein-1 (AP-1) activity and cyclooxygenase-2 (COX-2) expression in human mammary epithelial cells. The induction of COX-2 transcription by PMA was mediated by increased binding of AP-1 to the cyclic AMP response element (CRE) of the COX-2 promoter. Inhibition of the histone acetyltransferase activity of CREB- binding protein (CBP)/p300 blocked the induction of COX-2 by PMA. Treatment with carnosol but not RA blocked increased binding of AP-1 to the COX-2 promoter. Because AP-1 binding was unaffected by RA, we investigated whether RA inhibited COX-2 transcription via effects on the coactivator CBP/p300. Treatment with RA stimulated an interaction between RA receptor-alpha and CBP/p300; a corresponding decrease in the interaction between CBP/p300 and c-Jun was observed. Importantly, overexpressing CBP/p300 or dominant-negative RA receptor-alpha relieved the suppressive effect of RA on PMA-mediated stimulation of the COX-2 promoter. To elucidate the mechanism by which carnosol inhibited COX-2 transcription, its effects on protein kinase C (PKC) signaling were determined. Carnosol but not RA inhibited the activation of PKC, ERK1/2, p38, and c-Jun NH2-terminal kinase mitogen-activated protein kinase. Overexpressing c-Jun but not CBP/p300 reversed the suppressive effect of carnosol on PMA-mediated stimulation of COX-2 promoter activity. Thus, RA acted by a receptor-dependent mechanism to limit the amount of CBP/p300 that was available for AP-1-mediated induction of COX-2. By contrast, carnosol inhibited the induction of COX-2 by blocking PKC signaling and thereby the binding of AP-1 to the CRE of the COX-2 promoter. Taken together, these results show that small molecules can block the activation of COX-2 transcription by distinct mechanisms.
视黄酸(RA)或鼠尾草酸(两种具有抗癌特性但结构不相关的化合物)处理可抑制佛波酯(PMA)介导的人乳腺上皮细胞中激活蛋白-1(AP-1)活性的诱导和环氧合酶-2(COX-2)的表达。PMA对COX-2转录的诱导是通过AP-1与COX-2启动子的环磷酸腺苷反应元件(CRE)结合增加介导的。抑制CREB结合蛋白(CBP)/p300的组蛋白乙酰转移酶活性可阻断PMA对COX-2的诱导。鼠尾草酸处理而非RA处理可阻断AP-1与COX-2启动子结合的增加。由于AP-1结合不受RA影响,我们研究了RA是否通过对共激活因子CBP/p300的作用来抑制COX-2转录。RA处理可刺激RA受体α与CBP/p300之间的相互作用;同时观察到CBP/p300与c-Jun之间的相互作用相应减少。重要的是,过表达CBP/p300或显性负性RA受体α可减轻RA对PMA介导的COX-2启动子刺激的抑制作用。为了阐明鼠尾草酸抑制COX-2转录的机制,测定了其对蛋白激酶C(PKC)信号传导的影响。鼠尾草酸而非RA抑制PKC、细胞外信号调节激酶1/2(ERK1/2)、p38和c-Jun氨基末端激酶丝裂原活化蛋白激酶的激活。过表达c-Jun而非CBP/p300可逆转鼠尾草酸对PMA介导的COX-2启动子活性刺激的抑制作用。因此,RA通过受体依赖性机制发挥作用,限制可用于AP-1介导的COX-2诱导的CBP/p300的量。相比之下,鼠尾草酸通过阻断PKC信号传导从而阻断AP-1与COX-2启动子CRE的结合来抑制COX-2的诱导。综上所述,这些结果表明小分子可通过不同机制阻断COX-2转录的激活。