| Literature DB >> 24971532 |
Hongling Zhu1, Jin Fang2, Jichen Zhang1, Zefei Zhao1, Lianyong Liu1, Jingnan Wang1, Qian Xi1, Mingjun Gu3.
Abstract
In this study, we investigated the role and underlying mechanism of action of miR-182 in papillary thyroid carcinoma (PTC). Bioinformatics analysis revealed close homolog of LI (CHL1) as a potential target of miR-182. Upregulation of miR-182 was significantly correlated with CHL1 downregulation in human PTC tissues and cell lines. miR-182 suppressed the expression of CHL1 mRNA through direct targeting of the 3'-untranslated region (3'-UTR). Downregulation of miR-182 suppressed growth and invasion of PTC cells. Silencing of CHL1 counteracted the effects of miR-182 suppression, while its overexpression mimicked these effects. Our data collectively indicate that miR-182 in PTC promotes cell proliferation and invasion through direct suppression of CHL1, supporting the potential utility of miR-182 inhibition as a novel therapeutic strategy against PTC.Entities:
Keywords: CHL1; Invasion; Papillary thyroid carcinoma; Proliferation; miR-182
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Year: 2014 PMID: 24971532 DOI: 10.1016/j.bbrc.2014.06.073
Source DB: PubMed Journal: Biochem Biophys Res Commun ISSN: 0006-291X Impact factor: 3.575