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MiR-186 suppresses the growth and metastasis of bladder cancer by targeting NSBP1
BACKGROUND: Increasing evidence has shown that microRNAs function as oncogenes or tumor suppressors in human malignancies, but the roles of miR-186 in human bladder cancer (BC) is still unclear. METHODS: First, quantitative real-time PCR (qRT-PCR) was performed to detect miR-186 expression in bladde...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4546080/ https://www.ncbi.nlm.nih.gov/pubmed/26290438 http://dx.doi.org/10.1186/s13000-015-0372-3 |
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author | Yao, Kun He, Leye Gan, Yu Zeng, Qing Dai, Yingbo Tan, Jing |
author_facet | Yao, Kun He, Leye Gan, Yu Zeng, Qing Dai, Yingbo Tan, Jing |
author_sort | Yao, Kun |
collection | PubMed |
description | BACKGROUND: Increasing evidence has shown that microRNAs function as oncogenes or tumor suppressors in human malignancies, but the roles of miR-186 in human bladder cancer (BC) is still unclear. METHODS: First, quantitative real-time PCR (qRT-PCR) was performed to detect miR-186 expression in bladder cancer tissues and cell lines. Then, Bioinformatics analysis, combined with luciferase reporter assay demonstrated the target gene of miR-186. Finally, the roles of miR-186 in regulation of tumor proliferation and invasion were further investigated. RESULTS: Here, our study showed miR-186 was down-regulated in bladder cancer tissues and cell lines. Luciferase reporter assay showed that miR-186 targets NSBP1 3′-untranslated region (UTR) directly and suppresses NSBP1 (HMGN5) expression in human bladder cancer cells. NSBP1 siRNA- and miR-186-mediated NSBP1 knock-down experiments revealed that miR-186 suppresses cell proliferation and invasion through suppression of NSBP1 expression. Expression analysis of a set of epithelial-mesenchymal transition (EMT) markers showed that NSBP1 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: Our data first time identified miR-186 as the upstream regulator of NSBP1 and also suggest miR-186-suppressed NSBP1 as a novel therapeutic approach for bladder cancer. |
format | Online Article Text |
id | pubmed-4546080 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-45460802015-08-23 MiR-186 suppresses the growth and metastasis of bladder cancer by targeting NSBP1 Yao, Kun He, Leye Gan, Yu Zeng, Qing Dai, Yingbo Tan, Jing Diagn Pathol Research BACKGROUND: Increasing evidence has shown that microRNAs function as oncogenes or tumor suppressors in human malignancies, but the roles of miR-186 in human bladder cancer (BC) is still unclear. METHODS: First, quantitative real-time PCR (qRT-PCR) was performed to detect miR-186 expression in bladder cancer tissues and cell lines. Then, Bioinformatics analysis, combined with luciferase reporter assay demonstrated the target gene of miR-186. Finally, the roles of miR-186 in regulation of tumor proliferation and invasion were further investigated. RESULTS: Here, our study showed miR-186 was down-regulated in bladder cancer tissues and cell lines. Luciferase reporter assay showed that miR-186 targets NSBP1 3′-untranslated region (UTR) directly and suppresses NSBP1 (HMGN5) expression in human bladder cancer cells. NSBP1 siRNA- and miR-186-mediated NSBP1 knock-down experiments revealed that miR-186 suppresses cell proliferation and invasion through suppression of NSBP1 expression. Expression analysis of a set of epithelial-mesenchymal transition (EMT) markers showed that NSBP1 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: Our data first time identified miR-186 as the upstream regulator of NSBP1 and also suggest miR-186-suppressed NSBP1 as a novel therapeutic approach for bladder cancer. BioMed Central 2015-08-20 /pmc/articles/PMC4546080/ /pubmed/26290438 http://dx.doi.org/10.1186/s13000-015-0372-3 Text en © Yao et al. 2015 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/ (http://creativecommons.org/licenses/by/4.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Yao, Kun He, Leye Gan, Yu Zeng, Qing Dai, Yingbo Tan, Jing MiR-186 suppresses the growth and metastasis of bladder cancer by targeting NSBP1 |
title | MiR-186 suppresses the growth and metastasis of bladder cancer by targeting NSBP1 |
title_full | MiR-186 suppresses the growth and metastasis of bladder cancer by targeting NSBP1 |
title_fullStr | MiR-186 suppresses the growth and metastasis of bladder cancer by targeting NSBP1 |
title_full_unstemmed | MiR-186 suppresses the growth and metastasis of bladder cancer by targeting NSBP1 |
title_short | MiR-186 suppresses the growth and metastasis of bladder cancer by targeting NSBP1 |
title_sort | mir-186 suppresses the growth and metastasis of bladder cancer by targeting nsbp1 |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4546080/ https://www.ncbi.nlm.nih.gov/pubmed/26290438 http://dx.doi.org/10.1186/s13000-015-0372-3 |
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