Harper Curt E, Cook Leah M, Patel Brijesh B, Wang Jun, Eltoum Isam A, Arabshahi Ali, Shirai Tomoyuki, Lamartiniere Coral A
Department of Pharmacology and Toxicology, University of Alabama at Birmingham, Birmingham, Alabama 35294-0019, USA.
Prostate. 2009 Nov 1;69(15):1668-82. doi: 10.1002/pros.21017.
Chemoprevention utilizing dietary agents is an effective means to slow the development of prostate cancer. We evaluated the potential additive and synergistic effects of genistein and resveratrol for suppressing prostate cancer in the Simian Virus-40 T-antigen (SV-40 Tag) targeted probasin promoter rat model, a transgenic model of spontaneously developing prostate cancer.
Rats were fed genistein or resveratrol (250 mg/kg AIN-76A diet) alone and in combination, and a low-dose combination (83 mg genistein + 83 mg resveratrol/kg diet). Histopathology and mechanisms of action studies were conducted at 30 and 12 weeks of age, respectively.
Genistein, resveratrol, and the high-dose combination treatments suppressed prostate cancer. The low-dose combination did not elicit protection against prostate cancer and was most likely below the effective dose for causing significant histopathological changes. Total genistein and resveratrol concentrations in the blood reached 2,160 and 211 nM, respectively in rats exposed to the single treatments. Polyphenol treatments decreased cell proliferation and insulin-like growth factor-1 (IGF-1) protein expression in the prostate. In addition, genistein as a single agent induced apoptosis and decreased steroid receptor coactivator-3 (SRC-3) in the ventral prostate (VP).
Genistein and resveratrol, alone and in combination, suppress prostate cancer development in the SV-40 Tag model. Regulation of SRC-3 and growth factor signaling proteins are consistent with these nutritional polyphenols reducing cell proliferation and increasing apoptosis in the prostate.
利用膳食剂进行化学预防是减缓前列腺癌发展的有效手段。我们在猿猴病毒40 T抗原(SV - 40 Tag)靶向的前列腺素启动子大鼠模型(一种自发发展前列腺癌的转基因模型)中评估了染料木黄酮和白藜芦醇对抑制前列腺癌的潜在相加和协同作用。
给大鼠单独或联合喂食染料木黄酮或白藜芦醇(250毫克/千克AIN - 76A饲料),以及低剂量组合(83毫克染料木黄酮 + 83毫克白藜芦醇/千克饲料)。分别在30周龄和12周龄时进行组织病理学和作用机制研究。
染料木黄酮、白藜芦醇和高剂量组合处理均抑制了前列腺癌。低剂量组合未对前列腺癌产生保护作用,很可能低于引起显著组织病理学变化的有效剂量。接受单一处理的大鼠血液中染料木黄酮和白藜芦醇的总浓度分别达到2160纳摩尔和211纳摩尔。多酚处理降低了前列腺中的细胞增殖和胰岛素样生长因子 - 1(IGF - 1)蛋白表达。此外,染料木黄酮作为单一药剂诱导了腹侧前列腺(VP)中的细胞凋亡并降低了类固醇受体共激活因子 - 3(SRC - 3)。
染料木黄酮和白藜芦醇单独及联合使用均能抑制SV - 40 Tag模型中的前列腺癌发展。SRC - 3和生长因子信号蛋白的调节与这些营养多酚减少前列腺细胞增殖和增加细胞凋亡一致。