Zhang Jiacui, Jiao Keping, Liu Jing, Xia Yu
Department of Internal Medicine, The First Hospital of Lanzhou University, Lanzhou, Gansu 730000, P.R. China.
Department of Respiratory Medicine, People's Hospital of Gansu Province, Lanzhou, Gansu 730000, P.R. China.
Oncol Lett. 2018 Nov;16(5):6071-6080. doi: 10.3892/ol.2018.9382. Epub 2018 Sep 3.
The nuclear factor, erythroid 2 like 2 (Nrf2)/antioxidant response element (ARE) pathway has an important role in the drug resistance of adenocarcinoma, and may act via different mechanisms, including the mitogen-activated protein kinase (MAPK) pathway. However, it has remained elusive whether metformin affects Nrf2 and regulates Nrf2/ARE in adenocarcinoma. In the present study, reverse-transcription quantitative polymerase chain reaction, cell transfection, western blot analysis, a Cell Counting kit-8 assay and apoptosis detection were used to investigate the above in the A549 cell line and cisplatin-resistant A549 cells (A549/DDP). The results indicated that Nrf2, glutathione S-transferase α 1 (GSTA1) and ATP-binding cassette subfamily C member 1 (ABCC1) were dose-dependently reduced by metformin, and that the effect in A549 cells was greater than that in A549/DDP cells. Treatment with metformin decreased the proliferation and increased the apoptosis of A549 cells to a greater extent than that of A549/DDP cells, and the effect was dose-dependent. After transfection of A549/DDP cells with Nrf2 short hairpin RNA (shRNA), GSTA1 and ABCC1 were markedly decreased, compared with the shRNA-control group of A549/DDP, and low dose-metformin reduced the proliferation and increased apoptosis of A549/DDP cells. Metformin inhibited the Akt and extracellular signal-regulated kinase (ERK)1/2 pathways in A549 cells and activated the p38 MAPK and c-Jun N-terminal kinase (JNK) pathways. Furthermore, in the presence of metformin, inhibitors of the p38 MAPK and JNK signaling pathway at different concentrations did not affect the levels of Nrf2, but inhibitors of the Akt and ERK1/2 pathway at different doses reduced the expression of Nrf2. In addition, inhibitors of p38 MAPK and JNK did not affect the effect of metformin on Nrf2, while inhibitors of Akt and ERK1/2 dose-dependently enhanced the inhibitory effects of metformin in A549 cells. In conclusion, metformin inhibits the phosphoinositide-3 kinase/Akt and ERK1/2 signaling pathways in A549 cells to reduce the expression of Nrf2, GSTA1 and ABCC1. Metformin also reverses the resistance of A549/DDP cells to platinum drugs, inhibits the proliferation and promotes apoptosis of drug-resistant cells. These results may provide a theoretical basis and therapeutic targets for the clinical treatment of tumors.
核因子红细胞2样2(Nrf2)/抗氧化反应元件(ARE)通路在腺癌的耐药性中起重要作用,可能通过不同机制发挥作用,包括丝裂原活化蛋白激酶(MAPK)通路。然而,二甲双胍是否影响腺癌中的Nrf2并调节Nrf2/ARE仍不清楚。在本研究中,采用逆转录定量聚合酶链反应、细胞转染、蛋白质印迹分析、细胞计数试剂盒-8检测和凋亡检测,在A549细胞系和顺铂耐药的A549细胞(A549/DDP)中研究上述问题。结果表明,二甲双胍可使Nrf2、谷胱甘肽S-转移酶α1(GSTA1)和ATP结合盒亚家族C成员1(ABCC1)呈剂量依赖性降低,且对A549细胞的作用大于对A549/DDP细胞的作用。与A549/DDP细胞的短发夹RNA(shRNA)对照组相比,用Nrf2 shRNA转染A549/DDP细胞后,GSTA1和ABCC1明显降低,低剂量二甲双胍可降低A549/DDP细胞的增殖并增加其凋亡。二甲双胍抑制A549细胞中的Akt和细胞外信号调节激酶(ERK)1/2通路,并激活p38 MAPK和c-Jun氨基末端激酶(JNK)通路。此外,在存在二甲双胍的情况下,不同浓度的p38 MAPK和JNK信号通路抑制剂不影响Nrf2水平,但不同剂量的Akt和ERK1/2通路抑制剂可降低Nrf2的表达。此外,p38 MAPK和JNK抑制剂不影响二甲双胍对Nrf2的作用,而Akt和ERK1/2抑制剂可剂量依赖性增强二甲双胍对A549细胞的抑制作用。总之,二甲双胍抑制A549细胞中的磷酸肌醇-3激酶/Akt和ERK1/2信号通路,以降低Nrf2、GSTA1和ABCC1的表达。二甲双胍还可逆转A549/DDP细胞对铂类药物的耐药性,抑制耐药细胞的增殖并促进其凋亡。这些结果可能为肿瘤的临床治疗提供理论依据和治疗靶点。