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Metformin enhances the radiosensitizing effect of cisplatin in non-small cell lung cancer cell lines with different cisplatin sensitivities

机译:二甲双胍增强顺铂在具有不同顺铂敏感性的非小细胞肺癌细胞系中的放射增敏作用

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摘要

Cisplatin is an extensively used chemotherapeutic drug for lung cancer, but the development of resistance decreases its effectiveness in the treatments of non-small cell lung cancer (NSCLC). In this study, we examined the effects of metformin, a widely used antidiabetic drug, on cisplatin radiosensitization in NSCLC cell lines. Human NSCLC cell lines, A549 (cisplatin-resistant) and H460 (cisplatin-sensitive), were treated with metformin, cisplatin or a combination of both drugs before ionizing radiation. Cell proliferation, clonogenic assays, western blotting, cisplatin>-DNA adduct formation and immunocytochemistry were used to characterize the treatments effects. Metformin increased the radiosensitivity of NSCLC cells. Metformin showed additive and over-additive effects in combination with cisplatin and the radiation response in the clonogenic assay in H460 and A549 cell lines (p = 0.018 for the interaction effect between cisplatin and metformin), respectively. At the molecular level, metformin led to a significant increase in cisplatin-DNA adduct formation compared with cisplatin alone (p < 0.01, ANOVA-F test). This was accompanied by a decreased expression of the excision repair cross-complementation 1 expression (ERCC1), a key enzyme in nucleotide excision repair pathway. Furthermore, compared with each treatment alone metformin in combination with cisplatin yielded the lowest level of radiation>-induced Rad51 foci, an essential protein of homologous recombination repair. Ionizing radiation-induced γ-H2AX and 53BP1 foci persisted longer in both cell lines in the presence of metformin. Pharmacological inhibition of AMP-activated protein kinase (AMPK) demonstrated that metformin enhances the radiosensitizing effect of cisplatin through an AMPK-dependent pathway only in H460 but not in A549 cells. Our results suggest that metformin can enhance the effect of combined cisplatin and radiotherapy in NSCLC and can sensitize these cells to radiation that are not sensitized by cisplatin alone.
机译:顺铂是一种广泛用于肺癌的化疗药物,但耐药性的发展降低了其在非小细胞肺癌(NSCLC)治疗中的有效性。在这项研究中,我们检查了二甲双胍(一种广泛使用的抗糖尿病药)对NSCLC细胞系中顺铂放射增敏的作用。在电离辐射之前,先用二甲双胍,顺铂或两种药物的组合治疗人NSCLC细胞系A549(对顺铂耐药)和H460(对顺铂敏感)。细胞增殖,克隆形成测定,蛋白质印迹,顺铂>- DNA加合物形成和免疫细胞化学被用来表征治疗效果。二甲双胍增加了NSCLC细胞的放射敏感性。在H460和A549细胞系的成克隆测定中,二甲双胍与顺铂联合显示加性和超加性效应,且放射反应(顺铂和二甲双胍之间的相互作用效应分别为p = 0.018)。在分子水平上,与单独使用顺铂相比,二甲双胍导致顺铂-DNA加合物的形成显着增加(p <0.01,ANOVA-F测试)。这伴随着切除修复交叉互补1表达(ERCC1)的表达降低,ERCC1是核苷酸切除修复途径中的关键酶。此外,与每种单独治疗相比,二甲双胍联合顺铂产生最低水平的辐射>-诱导的Rad51病灶,这是同源重组修复的必需蛋白。在存在二甲双胍的情况下,电离辐射诱导的γ-H2AX和53BP1病灶在两种细胞系中持续更长的时间。 AMP激活的蛋白激酶(AMPK)的药理抑制作用表明,二甲双胍仅通过H460而非A549细胞通过AMPK依赖性途径增强顺铂的放射增敏作用。我们的结果表明,二甲双胍可以增强顺铂联合放疗在非小细胞肺癌中的作用,并且可以使这些细胞对仅由顺铂不敏感的放射线敏感。

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