Long Noncoding RNA LINC00460 Promotes the Gefitinib Resistance of Nonsmall Cell Lung Cancer Through Epidermal Growth Factor Receptor by Sponging miR-769-5p

被引:71
作者
Ma, Guodong [1 ]
Zhu, Jiping [2 ]
Liu, Feng [1 ]
Yang, Yan [3 ]
机构
[1] Nanjing Chest Hosp, Dept Chest Surg, Nanjing 210029, Jiangsu, Peoples R China
[2] Jiangsu Prov Hosp Tradit Chinese Med, Dept Pneumol, Nanjing, Jiangsu, Peoples R China
[3] Nanjing Med Univ, Dept Radiat Oncol, Affiliated Hosp 1, Nanjing 210029, Jiangsu, Peoples R China
关键词
nonsmall cell lung cancer; gefitinib resistance; LINC00460; miR-769-5p; EGFR; POOR-PROGNOSIS; INHIBITORS; PROGRESSION; DESIGN; EGFR;
D O I
10.1089/dna.2018.4462
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The vital roles of long noncoding RNAs (lncRNAs) in the nonsmall cell lung cancer (NSCLC) tumorigenesis are increasingly important. This work aims to investigate the role of lncRNA LINC00460 in the gefitinib resistance of NSCLC cells and discover its relevant mechanism. Our finding reveals that the expression of lncRNA LINC00460 is upregulated in the gefitinib-resistant NSCLC tissue and cells, and closely correlated with advanced tumor stage and clinical poor prognosis outcome. Gain and loss functional assays are performed in gefitinib-resistant NSCLC cells (A549/GR), stating that LINC00460 facilitates the 50% inhibitive concentration of gefitinib for NSCLC cells, multidrug-resistant-related proteins (P-gp, MRP1, and BCRP), as well as the invasion. In vivo, LINC00460 silencing represses the tumor growth. Bioinformatics prediction tools and luciferase analysis confirm that the upregulated LINC00460 sponged miR-769-5p in NSCLC cells; moreover, epidermal growth factor receptor (EGFR) is identified as a direct target gene of miR-769-5p. Verification experiments confirm that the restoration of EGFR could weaken the sensibility of NSCLC cells toward the gefitinib. In conclusion, our result demonstrates that LINC00460 plays a pivotal role in gefitinib resistance of NSCLC cells by targeting EGFR through sponging miR-769-5p. This finding might serve as a therapeutic target for NSCLC.
引用
收藏
页码:176 / 183
页数:8
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