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首页> 外文期刊>Archives of Biochemistry and Biophysics >Role of the retinoblastoma (pRb)-E2F/DP pathway in cancer chemopreventive effects of green tea polyphenol epigallocatechin-3-gallate
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Role of the retinoblastoma (pRb)-E2F/DP pathway in cancer chemopreventive effects of green tea polyphenol epigallocatechin-3-gallate

机译:视网膜母细胞瘤(pRb)-E2F / DP途径在绿茶多酚表没食子儿茶素-3-没食子酸酯的癌症化学预防作用中的作用

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摘要

Because of the demonstrated role of green tea polyphenol epigallocatechin-3-gallate (EGCG) in cancer chemoprevention, there is considerable emphasis in understanding its mechanism of action. In this study, we assessed the involvement of the retinoblastoma (pRb)-E2F/DP pathway as an important contributor in the antiproliferative effects of EGCG. As shown by immunoblot analysis, EGCG treatment of A431 cells resulted in a dose- as well as time-dependent decrease in the total pRb with a relative increase in the hypo-phosphorylated form of pRb. EGCG also resulted in serine-780 phosphorylation of pRb in these cells. Further, EGCG was found to downregulate the protein expression of other members of the pRb family, viz. p130 and p107, in a dose- as well as time-dependent manner. This response was accompanied by downregulation in the protein expression of the E2F (1 through 5) family of transcription factors and their heterodimeric partners DP1 and DP2. Taken together, our study suggests that EGCG causes a downregulation of hyperphosphorylated pRb protein with a relative increase in hypophosphorylated pRb that, in turn, compromises with the availability of "free" E2F. This series of events leads to stoppage of cell cycle progression at the G(1)-->S phase transition thereby causing G(0)/G(1) arrest and subsequent apoptotic cell death. This, to our knowledge, is the first study showing the involvement of the pRb-E2F/DP pathway in antiproliferative and apoptotic effects of EGCG. (C) 2002 Elsevier Science. [References: 50]
机译:由于绿茶中的多酚表没食子儿茶素-3-没食子酸酯(EGCG)在癌症化学预防中已显示出重要作用,因此在了解其作用机理方面有相当大的重视。在这项研究中,我们评估了视网膜母细胞瘤(pRb)-E2F / DP途径作为EGCG抗增殖作用的重要贡献者。如免疫印迹分析所示,EGCG对A431细胞的处理导致总pRb的剂量和时间依赖性降低,而pRb的次磷酸化形式则相对增加。 EGCG还导致这些细胞中pRb的丝氨酸780磷酸化。此外,发现EGCG下调了pRb家族其他成员的蛋白表达,即。 p130和p107呈剂量依赖性和时间依赖性。该响应伴随着转录因子E2F(1至5)家族及其异二聚体伴侣DP1和DP2的蛋白表达下调。两者合计,我们的研究表明EGCG会引起磷酸化pRb蛋白的下调,而磷酸化pRb的相对增加,反过来又会损害“游离” E2F的可用性。这一系列事件导致在G(1)-> S相转变处细胞周期进程停止,从而导致G(0)/ G(1)停滞并随后导致凋亡细胞死亡。据我们所知,这是第一项显示pRb-E2F / DP途径参与EGCG的抗增殖和凋亡作用的研究。 (C)2002 Elsevier科学。 [参考:50]

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