Cisplatin induced protective autophagy in A549 lung cancer cells and effects of Feiyanning decoction on expressions of autophagy proteins Atg5 and Atg7
ZHENG Zhan, MA Yue, WANG Qing, et al. Cisplatin induced protective autophagy in A549 lung cancer cells and effects of Feiyanning decoction on expressions of autophagy proteins Atg5 and Atg7[J]. Shanghai Journal of Traditional Chinese Medicine, 2018,52(4):77-80.
ZHENG Zhan, MA Yue, WANG Qing, et al. Cisplatin induced protective autophagy in A549 lung cancer cells and effects of Feiyanning decoction on expressions of autophagy proteins Atg5 and Atg7[J]. Shanghai Journal of Traditional Chinese Medicine, 2018,52(4):77-80. DOI: 10.16305/j.1007-1334.2018.04.022.
Objective:To observe the autophagy induced by cisplatin in A549 lung cancer cells and the effects of Feiyanning decoction on the autophagy related proteins including autophagy related gene 5 (Atg5) and autophagy related gene 7 (Atg7). MethodsThe A549 lung cancer cells were cultured and treated with cisplatin and Feiyanning decoction. The optimized concentrations of cisplatin and Feiyanning were screened by cell counting kit-8 (CCK-8) assay. The proliferation ability of A549 cells in each group was measured by CCK-8 assay. The expressions of autophagy related proteins in each group were detected by Western blot. Results:Compared with cisplatin alone,3 mg/L cisplatin combined with 20 mmol/L chloroquine(autophagy inhibitor)significantly increased the inhibition rate of A549 cell proliferation (P<0.05). Meanwhile,the protein expression of microtubule-associated protein 1 light chain 3(LC3Ⅱ)was increased after cisplatin treatment (P<0.01). The Atg5 protein expression in the Feiyanning group was lower than that in the model group and the cisplatin group (P<0.05),and the Atg7 protein expression in the Feiyanning group was significantly lower than that in the model group and the cisplatin group (P<0.01). Conclusion:Cisplatin induces protective autophagy in A549 lung cancer cells,and Feiyangning may suppress the cell proliferation by inhibiting autophagy in lung cancer cells.