miR-154 inhibits prostate cancer cell proliferation by targeting CCND2

被引:41
|
作者
Zhu, Chen [1 ]
Shao, Pengfei [1 ]
Bao, Meiling [1 ]
Li, Pu [1 ]
Zhou, Hai [1 ]
Cai, Hongzhou [1 ]
Cao, Qiang [1 ]
Tao, Liangjun [1 ]
Meng, Xiaoxin [1 ]
Ju, Xiaobing [1 ]
Qin, Chao [1 ]
Li, Jie [1 ]
Yin, Changjun [1 ]
机构
[1] Nanjing Med Univ, Affiliated Hosp 1, Dept Urol, State Key Lab Reprod Med, Nanjing, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
miR-154; Prostate cancer; CCND2; CYCLIN D1; EXPRESSION; OVEREXPRESSION; CARCINOMA; PROGRESSION; PROGNOSIS; COLON; LINES; P27;
D O I
10.1016/j.urolonc.2012.11.013
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Research has shown reduced expression levels of miR-154 in prostate cancer (CaP). However, the function and molecular mechanisms of miR-154 in this cancer type remains unknown. Objective: The aims of this study were to examine the functional significance of miR-154 in CaP cells and to identify the novel molecular targets regulated by miR-154. Materials and methods: miR-154 expression significantly decreased in primary CaP samples compared with nonmalignant samples measured by quantitative reverse transcription polymerase chain reaction. Restoration of miR-154 lowered the potential of CaP cell lines to grow and proliferate in vitro evaluated by CCK-8 assay, colony formation assay, and flow cytometry. miR-154 down-regulated the expression of CCND2 by binding to its 3'-untranslated region by luciferase reporter assay. Conclusions: miR-154 plays a prominent role in CaP proliferation by suppressing CCND2, and it may provide a new approach to the treatment of CaP. (C) 2014 Published by Elsevier Inc.
引用
收藏
页码:31.e9 / 31.e16
页数:8
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