首页> 美国卫生研究院文献>Journal of Zhejiang University. Science. B >Synergistic effects of tea polyphenols and ascorbic acid on human lung adenocarcinoma SPC-A-1 cells
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Synergistic effects of tea polyphenols and ascorbic acid on human lung adenocarcinoma SPC-A-1 cells

机译:茶多酚和抗坏血酸对人肺腺癌SPC-A-1细胞的协同作用

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摘要

Tea polyphenols have been shown to have ansticancer activity in many studies. In the present study, we investigated effects of theaflavin-3-3′-digallate (TF3), one of the major theaflavin monomers in black tea, in combination with ascorbic acid (AA), a reducing agent, and (−)-epigallocatechin-3-gallate (EGCG), the main polyphenol presented in green tea, in combination with AA on cellular viability and cell cycles of the human lung adenocarcinoma SPC-A-1 cells. The 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide (MTT) assay showed that the 50% inhibition concentrations (IC50) of TF3, EGCG, and AA on SPC-A-1 cells were 4.78, 4.90, and 30.62 μmol/L, respectively. The inhibitory rates of TF3 combined with AA (TF3+AA) and EGCG combined with AA (EGCG+AA) at a molar ratio of 1:6 on SPC-A-1 cells were 54.4% and 45.5%, respectively. Flow cytometry analysis showed that TF3+AA and EGCG+AA obviously increased the cell population in the G0/G1 phase of the SPC-A-1 cell cycle from 53.9% to 62.8% and 60.0%, respectively. TF3-treated cells exhibited 65.3% of the G0/G1 phase at the concentration of its IC50. Therefore, TF3+AA and EGCG+AA had synergistic inhibition effects on the proliferation of SPC-A-1 cells, and significantly held SPC-A-1 cells in G0/G1 phase. The results suggest that the combination of TF3 with AA or EGCG with AA enhances their anticancer activity.
机译:茶多酚已在许多研究中显示出具有抗癌活性。在本研究中,我们研究了茶黄素中主要的茶黄素单体之一茶黄素-3-3'-地戊二酸酯(TF3)与抗坏血酸(AA),还原剂和(-)-表没食子儿茶素的结合作用-3-没食子酸酯(EGCG)是绿茶中主要的多酚,与AA结合使用对人肺腺癌SPC-A-1细胞的细胞活力和细胞周期具有重要作用。 3-(4,5-二甲基噻唑-2-基)-2,5-二苯基溴化四唑(MTT)分析显示,TF3,EGCG和AA对SPC-A-1细胞的抑制浓度(IC50)为50%分别为4.78、4.90和30.62μmol/ L。 TF3与AA(TF3 + AA)和EGCG与AA(EGCG + AA)的摩尔比为1:6时,对SPC-A-1细胞的抑制率分别为54.4%和45.5%。流式细胞仪分析表明,TF3 + AA和EGCG + AA明显增加了SPC-A-1细胞周期G0 / G1期的细胞数量,分别从53.9%增至62.8%和60.0%。 TF3处理的细胞在其IC50浓度下表现出65.3%的G0 / G1相。因此,TF3 + AA和EGCG + AA对SPC-A-1细胞的增殖具有协同抑制作用,并显着地将SPC-A-1细胞保持在G0 / G1期。结果表明TF3与AA或EGCG与AA的组合增强了它们的抗癌活性。

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