| Literature DB >> 25998847 |
Tangwei Wu1, Weiqun Chen2, Deyong Kong1, Xiaoyi Li1, Hongda Lu3, Shuiyi Liu4, Jing Wang1, Lili Du1, Qingzhi Kong5, Xiaodong Huang6, Zhongxin Lu7.
Abstract
To determine the role of miR-25 in non-small cell lung cancer (NSCLC), we first detected miR-25 expression in clinical specimens and lung cancer cell lines by quantitative real-time polymerase chain reaction. The levels of miR-25 were elevated in the plasma of NSCLC patients and NSCLC cell lines. Transfection of A549 and 95-D cells with a miR-25 inhibitor resulted in reduced cell proliferation and enhanced apoptosis. Moreover, the modulator of apoptosis 1 (MOAP1) gene was identified as a novel target of miR-25. The ability of miR-25 to promote cell proliferation and block apoptosis is attributable to its effect on MOAP1 suppression. In addition, miR-25 antagomir significantly inhibited lung cancer growth via upregulation of MOAP1 in a mouse xenograft model. Collectively, these data demonstrate that miR-25 is an important biomarker for lung cancer, and miR-25 promotes cell proliferation and inhibits apoptosis in NSCLC cells by negatively regulating MOAP1 expression.Entities:
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Year: 2015 PMID: 25998847 DOI: 10.1093/carcin/bgv068
Source DB: PubMed Journal: Carcinogenesis ISSN: 0143-3334 Impact factor: 4.944