miRNA-375 regulates the cell survival and apoptosis of human non-small cell carcinoma by targeting HER2

被引:22
作者
Cheng, Longqiang [1 ]
Zhan, Bingxiang [1 ]
Luo, Peng [1 ]
Wang, Baolong [1 ]
机构
[1] Anhui Med Univ, Affiliated Prov Hosp, Dept Clin Lab, 17 Lujiang Rd, Hefei 230001, Anhui, Peoples R China
关键词
miR-375; non-small cell lung cancer cell; proliferation; apoptosis; HER2; LUNG-CANCER; MICRORNA; PROLIFERATION; INVASION; METASTASIS; EXPRESSION; MIGRATION; MECHANISM;
D O I
10.3892/mmr.2017.6112
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
micro (mi)-RNAs are a class of small non-coding RNAs that regulate gene expression by binding to the 3'-untranslated region of mRNA, which may lead to mRNA degradation or transcription regulation. Previous studies indicated that miRNAs are important for the pathogenesis of human cancer. miR-375 has been implicated in various tumor types; however, the biological activity in human non-small cell lung carcinoma (NSCLC) cells remains to be fully elucidated. The purpose of the present study was to investigate the biological importance of miR-375 in human NSCLC cells. The expression of miRNAs and mRNA was determined using reverse transcription-quantitative polymerase chain reaction. Cell proliferation was analyzed using a Cell Counting kit-8 assay. Cell apoptosis was analyzed using a fluorescence-activated cell sorting assay. The migration and invasion abilities of cells were evaluated using an in vivo mouse model. Dual-luciferase assay and western blotting were used to determine the potential target of miR-375. The results indicated that the expression of miR-375 in human NSCLC cells was significantly downregulated and induction of miR-375 may inhibit the proliferation of human NSCLC cells by inducing apoptosis. An animal model was used to determine that the upregulation of miR-375 inhibited the migration and invasion of A549 human NSCLC cells in vivo. It was also determined that human epidermal growth factor receptor 2 (HER-2) was a direct target gene of miR-375 and induction of miR-375 may reduce the expression of HER-2 in human NSCLC cells. These findings suggested that miR-375 may act as a potential therapeutic target for human NSCLC cancer in the future.
引用
收藏
页码:1387 / 1392
页数:6
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