Brown Powel H, Subbaramaiah Kotha, Salmon Amoi P, Baker Rebecca, Newman Robert A, Yang Peiying, Zhou Xi Kathy, Bissonnette Reid P, Dannenberg Andrew J, Howe Louise R
Breast Center, Department of Medicine, Baylor College of Medicine, Houston, Texas, USA.
Cancer Prev Res (Phila). 2008 Aug;1(3):208-14. doi: 10.1158/1940-6207.CAPR-08-0021.
The inducible prostaglandin synthase isoform cyclooxygenase-2 (COX-2) is overexpressed in approximately 40% of human breast carcinomas and in precancerous breast lesions, particularly in association with overexpression of human epidermal growth factor receptor 2 (HER2/neu). Experimental breast cancer can be suppressed by pharmacologic inhibition or genetic ablation of Cox-2, suggesting potential clinical utility of COX-2 inhibitors with respect to breast cancer. Importantly, several clinical trials have found reduced colorectal adenoma formation in individuals administered selective COX-2 inhibitors. However, such trials also identified increased cardiovascular risk associated with COX-2 inhibitor use. The goal of this research was to test whether improved chemopreventive efficacy could be achieved by combining submaximal doses of a selective COX-2 inhibitor and a retinoid X receptor-selective retinoid (rexinoid). The rate of HER2/neu-induced mammary tumor formation was substantially delayed by coadministration of the COX-2 inhibitor celecoxib (500 ppm in diet) and the rexinoid LGD1069 (10 mg/kg body weight; oral gavage) to MMTV/neu mice. Median time to tumor formation was increased from 304 to >600 days (P < 0.0001). The combination was substantially more effective than either drug individually. Similarly, potent suppression of aromatase activity was observed in mammary tissues from the combination cohort (44% of control; P < 0.001). Regulation of aromatase expression and activity by COX-derived prostaglandins is well established. Interestingly however, single agent LGD1069 significantly reduced mammary aromatase activity (71% of control; P < 0.001) without modulating eicosanoid levels. Our data show that simultaneous blockade of COX/prostaglandin signaling and retinoid X receptor-dependent transcription confers potent anticancer efficacy, suggesting a novel avenue for clinical evaluation.
诱导型前列腺素合酶同工型环氧化酶-2(COX-2)在约40%的人类乳腺癌及癌前乳腺病变中过度表达,尤其与人类表皮生长因子受体2(HER2/neu)的过度表达相关。实验性乳腺癌可通过对Cox-2进行药物抑制或基因剔除来抑制,这表明COX-2抑制剂在乳腺癌方面具有潜在临床应用价值。重要的是,多项临床试验发现,服用选择性COX-2抑制剂的个体结肠腺瘤形成减少。然而,此类试验也发现了与使用COX-2抑制剂相关的心血管风险增加。本研究的目的是测试联合使用亚最大剂量的选择性COX-2抑制剂和视黄酸X受体选择性类视黄醇(视黄酸类药物)是否能提高化学预防效果。将COX-2抑制剂塞来昔布(饮食中500 ppm)和视黄酸类药物LGD1069(10 mg/kg体重;口服灌胃)联合给予MMTV/neu小鼠,HER2/neu诱导的乳腺肿瘤形成速率显著延迟。肿瘤形成的中位时间从304天增加到>600天(P<0.0001)。该联合用药比单独使用任何一种药物都有效得多。同样,在联合用药组的乳腺组织中观察到芳香化酶活性受到强力抑制(为对照组的44%;P<0.001)。COX衍生的前列腺素对芳香化酶表达和活性的调节已得到充分证实。然而,有趣的是,单药LGD1069可显著降低乳腺芳香化酶活性(为对照组的71%;P<0.001),而不调节类花生酸水平。我们的数据表明,同时阻断COX/前列腺素信号传导和视黄酸X受体依赖性转录可赋予强大的抗癌功效,这为临床评估提供了一条新途径。