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Int. braz. j. urol ; 43(6): 1060-1067, Nov.-Dec. 2017. graf
Artigo em Inglês | LILACS | ID: biblio-892928

RESUMO

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.


Assuntos
Humanos , Masculino , Neoplasias da Próstata/genética , Neoplasias da Próstata/patologia , Regulação Neoplásica da Expressão Gênica/genética , Proteínas de Ciclo Celular/metabolismo , Regiões não Traduzidas/genética , Proteínas Supressoras de Tumor/metabolismo , MicroRNAs/fisiologia , Proliferação de Células/genética , Proteínas de Ligação a DNA/metabolismo , Reação em Cadeia da Polimerase em Tempo Real , Neoplasias da Próstata/mortalidade , Regulação para Baixo , Regulação para Cima , Proteínas de Ligação a RNA/metabolismo , MicroRNAs/antagonistas & inibidores , Linhagem Celular Tumoral , Invasividade Neoplásica
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