| Literature DB >> 26073258 |
Kai Wu1, Liucheng Yang2, Jianfeng Chen3, Haijun Zhao4, Jianjun Wang3, Shuai Xu5, Zonghai Huang6.
Abstract
miR-362-5p is down-regulated in high-risk neuroblastoma and can function as a tumor suppressor. However, its role remains poorly understood. We show that miR-362-5p is down-regulated in metastatic neuroblastoma compared with primary neuroblastoma. Overexpression of miR-362-5p inhibits cell proliferation, migration and invasion of neuroblastoma cells in vitro and suppresses tumor growth of neuroblastoma in vivo. Phosphatidylinositol 3-kinase (PI3K)-C2β is a target of miR-362-5p. Knockdown of PI3K-C2β by siRNA had a similar effect to overexpression of miR-362-5p on SH-SY5Y cells. Overexpression of PI3K-C2β partially reversed tumor-suppressive effects of miR-362-5p. We suggest that miR-362-5p suppresses neuroblastoma cell growth and motility, partially by targeting PI3K-C2β.Entities:
Keywords: Motility; Neuroblastoma; Phosphatidylinositol 3-kinase; Proliferation; miR-362-5p
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Year: 2015 PMID: 26073258 DOI: 10.1016/j.febslet.2015.05.056
Source DB: PubMed Journal: FEBS Lett ISSN: 0014-5793 Impact factor: 4.124