miR-34C Disrupts the Stemness of Purified CD133+ Prostatic Cancer Stem Cells

被引:9
|
作者
Chen, Yuan
Rao, Qun
Zhang, Huiping
Xu, Hua
Zhang, Cuntai
Zhuang, Qianyuan
Ye, Zhangqun [1 ]
机构
[1] Huazhong Univ Sci & Technol, Tongji Med Coll, Tongji Hosp, Dept Urol, Wuhan 430030, Peoples R China
关键词
ANDROGEN RECEPTOR; THERAPY; IDENTIFICATION; EXPRESSION; RESISTANCE; MICRORNA; PROMOTES;
D O I
10.1016/j.urology.2016.07.021
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVE To find the potential micro-RNA (miRNA) that could determine the fate of prostate cancer stem cells. MATERIALS AND METHODS We compared miRNA expression between our purified CD133(+) prostatic cancer stem cells (PCSCs) and CD133-cells. Sphere formation assay and matrigel-based cell invasion assay were applied to determine the stemness of CD133(+) PCSCs after our manipulation of miRNA using miRNA mimic or miRNA inhibitor. RESULTS In this study, we identified that miR-34C was under-expressed in the purified CD133(+) PCSCs and enforced introduction of miR-34C attenuated the stemness of CD133(+) PCSCs. Clinically, we also observed a negative correlation between miR-34C and CD133. CONCLUSION Our data strongly suggest that miR-34C may play essential role in conferring castration resistance by equilibrating PSCS population. (C) 2016 Elsevier Inc.
引用
收藏
页码:177.e1 / 177.e9
页数:9
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