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

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....

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Autores principales: Yao, Kun, Tang, Jing, Tang, Yuxing, Gan, Yu, Dai, Yingbo, He, Leye
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4842562/
http://dx.doi.org/10.21037/tau.2016.s264
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author Yao, Kun
Tang, Jing
Tang, Yuxing
Gan, Yu
Dai, Yingbo
He, Leye
author_facet Yao, Kun
Tang, Jing
Tang, Yuxing
Gan, Yu
Dai, Yingbo
He, Leye
author_sort Yao, Kun
collection PubMed
description 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.
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spelling pubmed-48425622016-05-09 AB264. MiR-186 inhibits the malignant behaviours of urothelial bladder cancer cell lines by targeting HMGN5 Yao, Kun Tang, Jing Tang, Yuxing Gan, Yu Dai, Yingbo He, Leye Transl Androl Urol Printed Abstracts 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. AME Publishing Company 2016-04 /pmc/articles/PMC4842562/ http://dx.doi.org/10.21037/tau.2016.s264 Text en 2016 Translational Andrology and Urology. All rights reserved.
spellingShingle Printed Abstracts
Yao, Kun
Tang, Jing
Tang, Yuxing
Gan, Yu
Dai, Yingbo
He, Leye
AB264. MiR-186 inhibits the malignant behaviours of urothelial bladder cancer cell lines by targeting HMGN5
title AB264. MiR-186 inhibits the malignant behaviours of urothelial bladder cancer cell lines by targeting HMGN5
title_full AB264. MiR-186 inhibits the malignant behaviours of urothelial bladder cancer cell lines by targeting HMGN5
title_fullStr AB264. MiR-186 inhibits the malignant behaviours of urothelial bladder cancer cell lines by targeting HMGN5
title_full_unstemmed AB264. MiR-186 inhibits the malignant behaviours of urothelial bladder cancer cell lines by targeting HMGN5
title_short AB264. MiR-186 inhibits the malignant behaviours of urothelial bladder cancer cell lines by targeting HMGN5
title_sort ab264. mir-186 inhibits the malignant behaviours of urothelial bladder cancer cell lines by targeting hmgn5
topic Printed Abstracts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4842562/
http://dx.doi.org/10.21037/tau.2016.s264
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