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Synergistic effect of black tea polyphenol theaflavin-33’-digallate with cisplatin against cisplatin resistant human ovarian cancer cells

机译:红茶多酚茶黄素33’-地高辛与顺铂对人顺铂耐药的卵巢癌细胞的协同作用

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摘要

Theaflavin-3, 3’-digallate (TF3) is a phenolic compound extracted from black tea. We previously demonstrated that TF3 selectively inhibited ovarian cancer cells. Ovarian cancer has high death rate because of acquired cisplatin resistance. We aimed to investigate the synergistic effect of TF3 and cisplatin (CDDP) against cisplatin resistant ovarian cancer cells. In the present study, combination treatment with TF3 and CDDP showed a synergistic cytotoxic effect in A2780/CP70 and OVCAR3 cells. Combination treatment showed a synergistic pro-apoptotic effect and synergistically induced G1/S phase cell cycle arrest. Synergistic apoptosis was accompanied by regulating protein expression of cleaved caspase 3/7, cytochrome c, Bax and Bcl-2. Combination treatment induced G1/S phase cell cycle arrest via regulating protein expression of cyclin A2, cyclin D1, cyclin E1 and CDK2/4. Combination treatment could synergistically down-regulate Akt phosphorylation in both cell lines. TF3 may be used as an adjuvant for the treatment of advanced ovarian cancer.
机译:Theaflavin-3,3'-digallate(TF3)是从红茶中提取的酚类化合物。我们先前证明了TF3选择性抑制卵巢癌细胞。由于获得性顺铂耐药性,卵巢癌死亡率高。我们旨在研究TF3和顺铂(CDDP)对顺铂耐药的卵巢癌细胞的协同作用。在本研究中,TF3和CDDP的联合治疗在A2780 / CP70和OVCAR3细胞中显示出协同的细胞毒性作用。联合治疗显示出协同的促凋亡作用和协同诱导的G1 / S期细胞周期停滞。协同凋亡伴随着调节裂解的胱天蛋白酶3/7,细胞色素c,Bax和Bcl-2的蛋白表达。联合治疗通过调节细胞周期蛋白A2,细胞周期蛋白D1,细胞周期蛋白E1和CDK2 / 4的蛋白表达诱导G1 / S期细胞周期停滞。联合治疗可以协同下调两种细胞系中的Akt磷酸化。 TF3可用作治疗晚期卵巢癌的佐剂。

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