Zhang Yan, Feng Xiuli, Li Tao, Yi Erpan, Li Yu
Departments of Respiratory Medicine, Qilu hospital of Shandong University, Jinan, Shandong, China.
Departments of Respiratory Medicine, People's Hospital of Qingzhou, Weifang, Shandong, China.
Cancer Med. 2017 Aug;6(8):1965-1975. doi: 10.1002/cam4.1133. Epub 2017 Jul 18.
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.
本研究旨在探讨二甲双胍联合培美曲塞对非小细胞肺癌(NSCLC)模型的治疗效果,并探索其相关分子机制。采用CCK8法检测二甲双胍和培美曲塞的半数最大抑制浓度(IC50)及联合指数(CI),以评估两药联合的抗增殖和治疗效果。运用流式细胞术(FCM)和侵袭实验评估不同处理的NSCLC细胞系凋亡率和侵袭能力的变化。通过蛋白质免疫印迹法检测凋亡标志物,以验证与抗增殖和促凋亡作用相关的数据。与对照组相比,二甲双胍单药治疗可抑制NSCLC细胞系的生长,并不同程度降低其侵袭能力(P<0.05)。在三种受试NSCLC细胞系中,与两药单药治疗相比,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著增加了HCC827细胞S期的细胞数量(P<0.001),联合治疗对A549和H1975细胞系无影响。我们发现,二甲双胍联合培美曲塞诱导的细胞凋亡比单独使用二甲双胍或培美曲塞更多(P<0.05),这一结果通过凋亡标志物得到了验证。这些结果表明,二甲双胍联合培美曲塞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,二甲双胍联合培美曲塞在体外可能对NSCLC细胞具有有益的抗肿瘤作用。