MiR-26a inhibits prostate cancer progression by repression of Wnt5a

被引:58
作者
Zhao, Shijia [1 ]
Ye, Xiangdong [2 ]
Xiao, Lei [3 ]
Lian, Xuexiong [1 ]
Feng, Yupeng [1 ]
Li, Feng [1 ]
Li, Li [1 ]
机构
[1] Guangzhou Med Univ, Affiliated Hosp 4, Dept Urol, Guangzhou 511447, Guangdong, Peoples R China
[2] Guangzhou Med Univ, Affiliated Hosp 1, Dept Urol, Microsurg Ctr, Guangzhou 510230, Guangdong, Peoples R China
[3] Guangzhou Med Univ, Affiliated Hosp 4, Dept Emergency, Guangzhou 511447, Guangdong, Peoples R China
关键词
Prostate cancer; Metastasis; Wnt5a; miR-26a; EXPRESSION; OVEREXPRESSION; MICRORNAS; GENE; EZH2; TRANSITIONS; MECHANISMS; BIOLOGY; CELLS; MYC;
D O I
10.1007/s13277-014-2206-4
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
MicroRNAs (miRNAs) are small noncoding RNAs that are involved in different biological processes by suppressing target gene expression. miRNA microarray analysis revealed a significant decrease of miR-26a in prostate cancer tissues versus their normal counterparts, but the role of miR-26a is needed to investigate. In the present study, we found that miR-26a expression was lower in prostate cancer tissues compared with their normal controls, so did the prostate cancer cells. Next, by lentivirus-mediated gain-of-function studies, it was showed that stable miR-26a inhibited cell proliferation, metastasis, and epithelial mesenchymal transition and induced G1 phase arrest in prostate cancer. It was predicted that Wnt5a was a potential target gene of miR-26a by bioinformatics analysis. Then, luciferase assay and Western blot analysis identified that Wnt5a was a new direct target gene of miR-26a and miR-26a inhibited prostate cancer progression via Wnt5a. Altogether, the findings suggested that miR-26a may function as a tumor suppressor in prostate cancer by targeting Wnt5a.
引用
收藏
页码:9725 / 9733
页数:9
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