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

Résumé

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.


Sujets)
Humains , Mâle , Tumeurs de la prostate/génétique , Tumeurs de la prostate/anatomopathologie , Régulation de l'expression des gènes tumoraux/génétique , Protéines du cycle cellulaire/métabolisme , Régions non traduites/génétique , Protéines suppresseurs de tumeurs/métabolisme , microARN/physiologie , Prolifération cellulaire/génétique , Protéines de liaison à l'ADN/métabolisme , Réaction de polymérisation en chaine en temps réel , Tumeurs de la prostate/mortalité , Régulation négative , Régulation positive , Protéines de liaison à l'ARN/métabolisme , microARN/antagonistes et inhibiteurs , Lignée cellulaire tumorale , Invasion tumorale
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