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.
journal_name
FEBS Lettjournal_title
FEBS lettersauthors
Qi X,Li J,Zhou C,Lv C,Tian Mdoi
10.1016/j.febslet.2014.08.021subject
Has Abstractpub_date
2014-10-16 00:00:00pages
3732-8issue
20eissn
0014-5793issn
1873-3468pii
S0014-5793(14)00623-1journal_volume
588pub_type
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