MiR-186 inhibits proliferation, migration, and invasion of non-small cell lung cancer cells by downregulating Yin Yang 1

被引:28
|
作者
Huang, Tonghai [1 ]
Wang, Guangsuo [1 ]
Yang, Lin [1 ]
Peng, Bin [1 ]
Wen, Yuxin [1 ]
Ding, Guanggui [1 ]
Wang, Zheng [1 ]
机构
[1] Jinan Univ, Shenzhen Peoples Hosp, Dept Thorac Surg, Clin Med Coll 2, Shenzhen 518020, Guangdong, Peoples R China
关键词
miR-186; YY1; cell proliferation; apoptosis; migration and invasion; non-small cell lung cancer; YIN YANG 1; PHASE-III TRIAL; CONCURRENT CHEMORADIATION; MESENCHYMAL TRANSITION; CONTRIBUTES; SENSITIVITY; METASTASIS; STATISTICS; PACLITAXEL; CISPLATIN;
D O I
10.3233/CBM-170670
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND: Non-small cell lung cancer (NSCLC) is the main type of lung cancer. While miR-186 is significantly reduced in lung cancer tissues and cells, its role in NSCLC has not been completely elucidated. MATERIAL AND METHODS: We used qRT-PCR and western blot methods to investigate the levels of miR-186 and YY1 in 21 pairs of NSCLC tissues. Dual luciferase reporter gene assays were performed to detect whether miR-186 directly targets YY1. Next, the roles of miR-186 and its target gene (YY1) in determining the proliferation, apoptosis and migration capabilities of selected cell lines (A549 and HCC827) were investigated by using miR-186 mimics or YY1 siRNA. RESULTS: Our results showed that miR-186 was downregulated and YYI was upregulated in NSCLC tissue, and miR-186 expression was negatively associated with YY1. Similarly, miR-186 was also downregulated and YY1 expression also was upregulated in both A549 and HCC827 cells; furthermore, miR-186 was found to directly target YY1. Cell proliferation, invasion, and migration, as well as apoptosis induction were more strongly inhibited by YY1 siRNA than by miR-186. CONCLUSION: Our results suggest that miR-186 and its target gene (YY1) could possibly serve as new prognostic biomarkers and therapeutic targets for treating NSCLC in humans.
引用
收藏
页码:221 / 228
页数:8
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