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Long non-coding RNA CA7-4通过提高细胞自噬水平增强肺癌细胞A594的顺铂耐药

2021-08-31周张杰蓝燕丽蓝翔蔡晓平

中国现代医生 2021年20期
关键词:耐药肺癌水平

周张杰  蓝燕丽  蓝翔  蔡晓平

[關键词] 肺癌;非小细胞肺癌;长链非编码RNA CA7-4;顺铂;耐药;自噬

[中图分类号] R329.2          [文献标识码] A          [文章编号] 1673-9701(2021)20-0035-05

Long non-coding RNA CA7-4 in enhancing cisplatin resistance of lung cancer cell A594 by increasing autophagy levels

ZHOU Zhangjie1   LAN Yanli2   LAN Xiang2   CAI Xiaoping3

1.Department of General Medicine, Lishui Central Hospital in Zhejiang Province, Lishui   323000, China; 2.Department of Oncology, Lishui People′s Hospital in Zhejiang Province, Sixth Affiliated Hospital of Wenzhou Medical Univevsity, Lishui   323000, China; 3.Department of Respiratory Medicine, Lishui People′s Hospital in Zhejiang Province, Sixth Affiliated Hospital of Wenzhou Medical Univevsity, Lishui   323000, China

[Abstract] Objective To analyze the mechanism of long non-coding RNA (LncRNA) CA7-4 in affecting cisplatin (DDP) resistance in non-small cell lung cancer (NSCLC) cell line A549. Methods The human NSCLC cell line A549 was cultured in different concentrations of DDP, and the cell viability was measured to calculate the half maximal inhibitory concentration (IC50). The A549 cells were divided into control group, DDP group, CA7-4 group and CA7-4+DDP group.The CA7-4 group and CA7-4+DDP group were transfected with CA7-4 pcDNA to up-regulate the level of LncRNA CA7-4. DDP group and CA7-4+DDP group were added with DDP at a final concentration of 12 μM. The cell viability, apoptosis rate and autophagy protein LC3Ⅰ and LC3Ⅱ levels of each group of cells were detected and compared. Results DDP can inhibit the growth of A549 cells in a dose-dependent manner. The IC50 value in this study was 12 μM. The level of LncRNA CA7-4 in the DDP group was significantly lower than that in the control group. The level of LncRNA CA7-4 in the CA7-4 group was significantly higher than that in the control group, and the LncRNA CA7-4 in the CA7-4+DDP group was significantly higher than that in the DDP group. The cell viability of the DDP group was significantly decreased and the apoptosis rate was significantly increased. The cell viability of the CA7-4 group was increased, and the apoptosis rate was decreased. The cell viability of the CA7-4+DDP group was significantly higher than that of the DDP group, while the apoptosis rate was significantly lower than that of the DDP group. The level of LC3Ⅱ/LC3Ⅰ in the DDP group was lower than that in the control group. The level of LC3Ⅱ/LC3Ⅰ in the CA7-4 group was higher than that in the control group. The level of LC3Ⅱ/LC3Ⅰ in the CA7-4+DDP group was significantly higher than that in the DDP group. Conclusion LncRNA CA7-4 can promote cell viability and inhibit cell apoptosis by promoting autophagy of NSCLC cell line A549, and promote cell resistance to DDP.


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