| Literature DB >> 25647033 |
XianJin Wu1, Yong Zeng2, ShaoKe Wu2, JiXin Zhong3, YuZhou Wang3, JunFa Xu4.
Abstract
Aberrant expression of miR-204 had been frequently reported in cancer studies; however, the mechanism of its function in retinoblastoma remained unknown. Here, we reported that miR-204 was frequently downregulated in retinoblastoma tissues and cell lines. Enforced expression of miR-204 inhibited retinoblastoma cells' proliferation and invasion. In vivo study indicated that restoration of miR-204 inhibited tumor growth. CyclinD2 and MMP-9 were identified as potential targets of miR-204. In addition, a reverse correlation between miR-204 and CyclinD2 or MMP-9 expression was noted in retinoblastoma tissues. Taken together, our results identified a crucial tumor suppressive role of miR-204 in the progression of retinoblastoma.Entities:
Keywords: CyclinD2; MMP-9; Retinoblastoma; miR-204
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Year: 2015 PMID: 25647033 DOI: 10.1016/j.febslet.2015.01.030
Source DB: PubMed Journal: FEBS Lett ISSN: 0014-5793 Impact factor: 4.124