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Genistein abrogates G2 arrest induced by curcumin in p53 deficient T47D cells

机译:金雀异黄素消除了姜黄素在p53缺陷T47D细胞中诱导的G2阻滞

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摘要

BackgroundThe high cost and low level of cancer survival urge the finding of new drugs having better mechanisms. There is a high trend of patients to be “back to nature” and use natural products as an alternative way to cure cancer. The fact is that some of available anticancer drugs are originated from plants, such as taxane, vincristine, vinblastine, pacitaxel. Curcumin (diferuloylmethane), a dietary pigment present in Curcuma longa rizhome is reported to induce cell cycle arrest in some cell lines. Other study reported that genistein isolated from Glycine max seed inhibited phosphorylation of cdk1, gene involved during G2/M transition and thus could function as G2 checkpoint abrogator. The inhibition of cdk1 phosphorylation is one of alternative strategy which could selectively kill cancer cells and potentially be combined with DNA damaging agent such as curcumin.
机译:背景技术高成本和低癌症存活率促使人们寻找具有更好机理的新药。患者趋于“回归自然”并使用天然产物作为治疗癌症的替代方法的可能性很高。事实是,一些可用的抗癌药都来自植物,例如紫杉烷,长春新碱,长春碱,紫杉醇。据报道,姜黄素(二氟甲酰甲烷)是一种存在于姜黄中的饮食色素,可诱导某些细胞系的细胞周期停滞。其他研究报道,从大豆最大种子中分离出的染料木黄酮抑制了cdk1的磷酸化,该基因在G2 / M过渡过程中涉及,因此可以作为G2检查点废止剂。抑制cdk1磷酸化是另一种策略,它可以选择性地杀死癌细胞,并可能与姜黄素等DNA破坏剂结合使用。

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