Bianco Nicole R, Chaplin Laura J, Montano Monica M
Department of Pharmacology, Case Western Reserve University, Cleveland, OH 44106, USA.
Biochem J. 2005 Jan 1;385(Pt 1):279-87. doi: 10.1042/BJ20040959.
Quinone reductase (QR) is a phase II detoxification enzyme that plays an important role in detoxifying quinones and may help maintain the antioxidant function of the cell. We have previously observed that QR is up-regulated by anti-oestrogens, but not oestrogen, in breast cancer cells via ERbeta (oestrogen receptor beta) transactivation. Such QR induction appears to protect breast cells against oestrogen-induced oxidative DNA damage, most likely by reducing reactive oestrogen metabolites termed catecholestrogen-quinones back to the hydroxy-catecholestrogens which may be conjugated. We now report that the phytoestrogens biochanin A, genistein and resveratrol also up-regulate QR expression in breast cancer cells. We observe that regulation can occur at the transcriptional level, preferentially through ERbeta transactivation at the electrophile response element of the QR gene promoter. By chromatin immunoprecipitation analysis, we show binding of ERalpha and ERbeta to the QR promoter, with increased ERbeta binding in the presence of resveratrol. Functional studies show that biochanin A and resveratrol, but not genistein, can significantly protect against oestrogen-induced oxidative DNA damage in breast cancer cells. Antisense technology was used to determine whether such protection was dependent on ERbeta or QR. Our results with resveratrol are consistent with our hypothesis that the protective ability of resveratrol is partially dependent on the presence of ERbeta and QR. In conclusion, we postulate that phytoestrogen-mediated induction of QR may represent an additional mechanism for breast cancer protection, although the effects may be specific for a given phytoestrogen.
醌还原酶(QR)是一种II相解毒酶,在醌解毒过程中发挥重要作用,并可能有助于维持细胞的抗氧化功能。我们之前观察到,在乳腺癌细胞中,抗雌激素通过雌激素受体β(ERβ)反式激活上调QR,而雌激素则不会。这种QR诱导似乎能保护乳腺细胞免受雌激素诱导的氧化性DNA损伤,很可能是通过将称为儿茶酚雌激素-醌的活性雌激素代谢物还原为可能被结合的羟基儿茶酚雌激素。我们现在报告,植物雌激素染料木黄酮、染料木素和白藜芦醇也能上调乳腺癌细胞中的QR表达。我们观察到这种调节可发生在转录水平,优先通过QR基因启动子亲电反应元件处的ERβ反式激活。通过染色质免疫沉淀分析,我们显示ERα和ERβ与QR启动子结合,在白藜芦醇存在下ERβ结合增加。功能研究表明,染料木黄酮和白藜芦醇而非染料木素能显著保护乳腺癌细胞免受雌激素诱导的氧化性DNA损伤。利用反义技术确定这种保护是否依赖于ERβ或QR。我们对白藜芦醇的研究结果与我们的假设一致,即白藜芦醇的保护能力部分依赖于ERβ和QR的存在。总之,我们推测植物雌激素介导的QR诱导可能是乳腺癌保护的另一种机制,尽管其作用可能因特定植物雌激素而异。