| Article ID | Journal | Published Year | Pages | File Type | 
|---|---|---|---|---|
| 10870256 | FEBS Letters | 2014 | 7 Pages | 
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 3â² 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.
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											Authors
												Xiaoming Qi, Jianqiang Li, Changbo Zhou, Chunlei Lv, Min Tian, 
											