miR-154 inhibits prostate cancer cell proliferation by targeting CCND2

Abstract 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 an...

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Veröffentlicht in:Urologic oncology 2014, Vol.32 (1), p.31.e9-31.e16
Hauptverfasser: Zhu, Chen, M.S, Shao, Pengfei, M.D., Ph.D, Bao, Meiling, M.S, Li, Pu, M.S, Zhou, Hai, M.S, Cai, Hongzhou, M.S, Cao, Qiang, M.S, Tao, Liangjun, M.S, Meng, Xiaoxin, M.D., Ph.D, Ju, Xiaobing, M.D., Ph.D, Qin, Chao, M.D., Ph.D, Li, Jie, M.D., Ph.D, Yin, Changjun, M.D., Ph.D
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Sprache:eng
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Zusammenfassung:Abstract 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.
ISSN:1078-1439
1873-2496
DOI:10.1016/j.urolonc.2012.11.013