The Downregulation of miR-200c Promotes Lactate Dehydrogenase A Expression and Non-Small Cell Lung Cancer Progression

被引:15
|
作者
Wei Lei [1 ]
Wang Kang [1 ]
Yang Nan [1 ]
Zhang Lei [1 ]
Li Zhongdong [1 ]
Li Demin [1 ]
Sun Lei [1 ]
Huang Hairong [1 ]
机构
[1] Nanjing Univ, Nanjing Jinling Hosp, Sch Med, Dept Cardiothorac Surg, 305 Zhongshan Dong Rd, Nanjing 210002, Jiangsu, Peoples R China
关键词
miR-200c; Non-small cell lung cancer (NSCLC); Lactate dehydrogenase A (LDHA); Cell proliferation; Cell migration; EPITHELIAL-MESENCHYMAL TRANSITION; SIGNALING PATHWAY; SUPPRESSES; INVASION; CHINA; PROLIFERATION; SENSITIVITY; METASTASIS; INHIBITION; MIGRATION;
D O I
10.3727/096504018X15151486241153
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
This study was aimed to investigate the function and mechanism of microRNA-200c (miR-200c) in the progression of non-small cell lung cancer ( NSCLC). A total of 76 patients diagnosed as having NSCLC were enrolled in this study. The expression level of miR-200c in NSCLC tissues and cell lines was investigated using the quantitative real-time polymerase chain reaction (RT-qPCR) method. We found that the expression of miR-200c was significantly reduced in NSCLC tissues and cell lines compared with normal lung tissues and the human bronchial epithelial cell line. Overexpression of miR-200c using the miR-200c mimic significantly suppressed cell proliferation and migration of NSCLC cell lines. The results of the luciferase reporter assay identified lactate dehydrogenase A (LDHA) as a direct target of miR-200c. The expression of LDHA was shown to be suppressed in NSCLC cell lines with miR-200c mimic transfection. Furthermore, the transfection of small interfering RNA (siRNA) targeting LDHA suppressed the proliferation and migration of NSCLC cell lines. In summary, our results presented in this study suggested that miR-200c was able to inhibit the proliferation and migration of NSCLC cells by downregulating LDHA. Therefore, miR-200c may be considered as a potential candidate for the treatment of NSCLC.
引用
收藏
页码:1015 / 1022
页数:8
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