AB264. MiR-186 inhibits the malignant behaviours of urothelial bladder cancer cell lines by targeting HMGN5
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AB264. MiR-186 inhibits the malignant behaviours of urothelial bladder cancer cell lines by targeting HMGN5

Kun Yao, Jing Tang, Yuxing Tang, Yu Gan, Yingbo Dai, Leye He

Department of Urology, The Third Xiangya Hospital of Central South University, Hunan 410013, China


Background: To investigate the role of miR-186 in the carcinogenesis and metastasis of human urothelial bladder cancer and its potential target protein.

Methods: Quantitative real-time PCR (qRT-PCR) was performed to detect miR-186 expression in human urothelial bladder cancer tissues and cell lines. Then, Bioinformatics analysis, combined with luciferase reporter assay demonstrated the miR-186’s target gene and protein. Finally, the roles of miR-186 in regulation of tumor proliferation and invasion were further investigated by MTT assay and transwell assay.

Results: MiR-186 was down-regulated in human urothelial bladder cancer tissues and cell lines. Luciferase reporter assay showed that miR-186 targets HMGN5 3'-untranslated region (UTR) directly and suppresses HMGN5 expression in human urothelial bladder cancer cells. HMGN5 siRNA- and miR-186-mediated HMGN5 knock-down experiments revealed that miR-186 suppresses cell proliferation and invasion through suppression of HMGN5 expression. Expression analysis of a set of epithelial-mesenchymal transition (EMT) markers showed that HMGN5 involves miR-186 suppressed EMT which reducing the expression of mesenchymal markers (vimentin and N-cadherin) and inducing the expression of epithelial marker (E-cadherin).

Conclusions: MiR-186 is the upstream regulator of HMGN5. MiR-186-suppressed HMGN5 is a potential novel therapeutic approach for human urothelial bladder cancer.

Keywords: miR-186; urothelial bladder cancer; HMGN5; regulation


doi: 10.21037/tau.2016.s264


Cite this abstract as: Yao K, Tang J, Tang Y, Gan Y, Dai Y, He L. MiR-186 inhibits the malignant behaviours of urothelial bladder cancer cell lines by targeting HMGN5. Transl Androl Urol 2016;5(Suppl 1):AB264. doi: 10.21037/tau.2016.s264

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