miR-483-5p promotes prostate cancer cell proliferation and invasion by targeting RBM5
Int. braz. j. urol; 43 (6), 2017
Publication year: 2017
ABSTRACT Objective:
miR-483-5p has been identified as a miRNA oncogene in certain cancers. However, its role in prostate cancer has not been sufficiently investigated. In this study, we investigated the role of miR-483-5p in prostate cancer and examined RBM5 regulation by miR-483-5p.Material and methods:
Expression levels of miR-483-5p were determined by quantitative real-time PCR. The effect of miR-483-5p on proliferation was evaluated by MTT assay, cell invasion was evaluated by trans-well invasion assays, and target protein expression was determined by western blotting in LNCaP, DU-145, and PC-3 cells. Luciferase reporter plasmids were constructed to confirm the action of miR-483-5p on downstream target gene RBM5 in HEK-293T cells.Results:
we observed that miR-483-5p was upregulated in prostate cancer cell lines and tissues. A miR-483-5p inhibitor inhibited prostate cancer cell growth and invasion in DU-145 and PC-3 cells. miR-483-5p directly bound to the 3' untranslated region (3'UTR) of RBM5 in HEK-293T cells. RBM5 overexpression inhibited prostate cancer cell growth and invasion in LNCaP cells. Enforced RBM5 expression alleviated miR-483-5p promotion of prostate cancer cell growth and invasion in LNCaP cells.Conclusion:
The present study describes a potential mechanism underlying a miR-483-5p/RBM5 link that contributes to prostate cancer development.
Regiones no Traducidas/genética, Proteínas de Ciclo Celular/metabolismo, Línea Celular Tumoral, Proliferación Celular/genética, Proteínas de Unión al ADN/metabolismo, Regulación hacia Abajo, Regulación Neoplásica de la Expresión Génica/genética, MicroARNs/antagonistas & inhibidores, MicroARNs/fisiología, Invasividad Neoplásica, Neoplasias de la Próstata/genética, Neoplasias de la Próstata/mortalidad, Neoplasias de la Próstata/patología, Proteínas de Unión al ARN/metabolismo, Reacción en Cadena en Tiempo Real de la Polimerasa, Proteínas Supresoras de Tumor/metabolismo, Regulación hacia Arriba