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Metformin synergistic pemetrexed suppresses non-small-cell lung cancer cell proliferation and invasion in vitro

机译:二甲双胍协同培美曲塞可抑制非小细胞肺癌细胞的体外增殖和侵袭

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Abstract The aim of this study was to investigate whether metformin in combination with pemetrexed has an effect on the treatment of non-small-cell lung cancer (NSCLC) models and to explore the related molecular mechanism. The half maximal inhibitory concentration (IC50) and combination index (CI) of metformin and pemetrexed were detected by the CCK8 assay to assess the antiproliferative and therapeutic effects of the two-drug combination. Flow cytometry (FCM) and invasion assays were used to estimate the variation in apoptosis rate and invasion ability of the differently treated NSCLC cell lines. Apoptotic markers were detected by western blotting to validate the data related to the antiproliferation and proapoptosis effects. Metformin monotherapy inhibited the growth of NSCLC cell lines and reduced the invasion ability to different degrees compared with the control groups ( P < 0.05). Metformin in combination with pemetrexed produced a synergistic effect (CI < 0.90) compared with the two drugs in monotherapy in the three tested NSCLC cell lines. Metformin in combination with pemetrexed significantly increased the cell numbers of HCC827 cells at S phase ( P < 0.001), and the combination therapy had no influence on the A549 and H1975 cell lines. We found that combining metformin with pemetrexed induced more cell apoptosis than metformin or pemetrexed used alone ( P < 0.05), which was validated by the apoptotic markers. These results demonstrate that the combination of metformin and pemetrexed has a synergistic effect on the treatment of NSCLC cell lines by inducing apoptosis or blocking the cell cycle. Our data indicate that the combination of metformin and pemetrexed could have beneficial antitumor effects on NSCLC cells in vitro.
机译:摘要目的探讨二甲双胍联合培美曲塞对非小细胞肺癌(NSCLC)模型的治疗是否有效,并探讨相关的分子机制。通过CCK8测定法检测二甲双胍和培美曲塞的半数最大抑制浓度(IC50)和组合指数(CI),以评估两种药物组合的抗增殖和治疗作用。流式细胞仪(FCM)和侵袭实验被用来评估不同处理的NSCLC细胞系的凋亡率和侵袭能力的变化。通过蛋白质印迹检测凋亡标记,以验证与抗增殖和凋亡作用有关的数据。与对照组相比,二甲双胍单药治疗可抑制NSCLC细胞系的生长,并不同程度地降低其侵袭能力(P <0.05)。在两种测试的NSCLC细胞系中,与单一疗法中的两种药物相比,二甲双胍联合培美曲塞产生了协同效应(CI <0.90)。二甲双胍联合培美曲塞显着增加了S期HCC827细胞的细胞数量(P <0.001),并且联合治疗对A549和H1975细胞系没有影响。我们发现二甲双胍与培美曲塞联用比单独使用二甲双胍或培美曲塞能诱导更多的细胞凋亡(P <0.05),这已被凋亡标记物证实。这些结果表明二甲双胍和培美曲塞的组合通过诱导凋亡或阻断细胞周期对NSCLC细胞系的治疗具有协同作用。我们的数据表明,二甲双胍和培美曲塞的组合可能在体外对NSCLC细胞具有有益的抗肿瘤作用。

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