| Literature DB >> 25171860 |
Xiaoming Qi1, Jianqiang Li1, Changbo Zhou1, Chunlei Lv1, Min Tian2.
Abstract
In the present study, we investigated the roles and molecular mechanisms of miR-320a in human nasopharyngeal carcinoma (NPC). miR-320a expression was strongly reduced in NPC tissues and cell lines. Overexpression of miR-320a significantly suppressed NPC cell growth, migration, invasion and tumor growth in a xenograft mouse model. A luciferase reporter assay revealed that miR-320a could directly bind to the 3' UTR of BMI-1. Overexpression of BMI-1 rescued miR-320a-mediated biological function. BMI-1 expression was found to be up-regulated and inversely correlated with miR-320a expression in NPC. Collectively, our data indicate that miR-320a plays a tumor suppressor role in the development and progression of NPC and may be a novel therapeutic target against NPC.Entities:
Keywords: BMI-1; Invasion; Nasopharyngeal carcinoma; Proliferation; miR-320a
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Year: 2014 PMID: 25171860 DOI: 10.1016/j.febslet.2014.08.021
Source DB: PubMed Journal: FEBS Lett ISSN: 0014-5793 Impact factor: 4.124