MicroRNA-139-5p inhibits bladder cancer proliferation and self-renewal by targeting the Bmi1 oncogene

被引:40
作者
Luo, Hongbo [1 ]
Yang, Rui [1 ]
Li, Chun [2 ]
Tong, Yongqing [3 ]
Fan, Lingling [2 ]
Liu, Xiuheng [1 ]
Xu, Chuanrui [2 ]
机构
[1] Wuhan Univ, Renmin Hosp, Dept Urol, Wuhan 430060, Hubei, Peoples R China
[2] Huazhong Univ Sci & Technol, Tongji Med Coll, Sch Pharm, Wuhan, Hubei, Peoples R China
[3] Wuhan Univ, Renmin Hosp, Dept Clin Lab, Wuhan, Hubei, Peoples R China
基金
中国国家自然科学基金;
关键词
MiR-139-5p; bladder cancer; Bmi1; cancer stem cell; HEPATOCELLULAR-CARCINOMA CELLS; COLORECTAL-CANCER; MIR-139-5P; INVASION; APOPTOSIS; MIGRATION; GROWTH; CYCLE;
D O I
10.1177/1010428317718414
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
MiR-139-5p has been reported to be overexpressed in many types of cancers, but its role in bladder cancer has not been elucidated yet. Here, we report that miR-139-5p functions as a tumor suppressor in bladder cancer and inhibits the cancer stem cell self-renewal by targeting Bmi1 directly. We found that miR-139-5p expression was significantly downregulated in the bladder cancer specimens compared with that in adjacent normal tissues. In vitro, restoration of miR-139-5p expression significantly inhibited the proliferation of bladder cancer cells. Mechanism analysis revealed that miR-139-5p could decrease Bmi1 protein levels by binding to the 3' untranslated region of Bmi1 messenger RNA. Stem cell-related proteins such as c-MYC, NANOG, OCT4, and KLF4 and signaling pathways such as Wnt signaling were suppressed by restoration of miR-139-5p in bladder cancer cells. In addition, miR-139-5p expression also blocked selfrenewal of bladder cancer stem cells by inhibiting Bmi1. In summary, our study supports that miR-139-5p acts as a tumor suppressor in bladder cancer development and suppresses cancer stem cell property of bladder cancer. Our study also suggests that miR-139-5p has the potential to be used as a therapeutic molecule for bladder cancer treatment.
引用
收藏
页数:8
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