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miR-203 Suppresses Bladder Cancer Cell Growth and Targets Twist1
miR-203 is an epigenetically silenced tumor-suppressive microRNA in tumors. This study was designed to investigate the effects of miR-203 on the proliferation, migration, invasion, and apoptosis of bladder cancer (BCa) cells. The expression levels of miR-203 in BCa tissues, normal adjacent tissues,...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cognizant Communication Corporation
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7844766/ https://www.ncbi.nlm.nih.gov/pubmed/28893347 http://dx.doi.org/10.3727/096504017X15041934685237 |
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author | Shen, Jie Zhang, Jianhua Xiao, Minhui Yang, Junfeng Zhang, Ningnan |
author_facet | Shen, Jie Zhang, Jianhua Xiao, Minhui Yang, Junfeng Zhang, Ningnan |
author_sort | Shen, Jie |
collection | PubMed |
description | miR-203 is an epigenetically silenced tumor-suppressive microRNA in tumors. This study was designed to investigate the effects of miR-203 on the proliferation, migration, invasion, and apoptosis of bladder cancer (BCa) cells. The expression levels of miR-203 in BCa tissues, normal adjacent tissues, and BCa cell lines were detected. BCa cells were transfected with miR-203 mimic and inhibitor to investigate the effect of miR-203 on cell functions and the epithelial–mesenchymal transition (EMT). Cotransfection with miR-203 inhibitor and shRNA of the predicted target gene Twist1 (si-Twist1) was performed to investigate the target relationship of miR-203 and Twist1. The effects of knockdown of Twist1 on cell functions were also investigated. The expression of miR-203 was significantly reduced in BCa tissues and cells, in comparison with the control. miR-203 mimic significantly reduced cell viability, invasion, migration, and EMT, and enhanced cell apoptosis. On the contrary, miR-203 inhibitor showed the opposite results. However, the administration of si-Twist1 cancelled the effect of miR-203 inhibitor on cell proliferation, apoptosis, invasion, and migration. These demonstrated that miR-203 may function as a tumor-suppressive microRNA in BCa by negatively targeting Twist1. Both Twist1 and miR-203 might be explored as potential targets for studying the mechanism related to BCa pathogenesis and therapy. |
format | Online Article Text |
id | pubmed-7844766 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Cognizant Communication Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-78447662021-02-16 miR-203 Suppresses Bladder Cancer Cell Growth and Targets Twist1 Shen, Jie Zhang, Jianhua Xiao, Minhui Yang, Junfeng Zhang, Ningnan Oncol Res Article miR-203 is an epigenetically silenced tumor-suppressive microRNA in tumors. This study was designed to investigate the effects of miR-203 on the proliferation, migration, invasion, and apoptosis of bladder cancer (BCa) cells. The expression levels of miR-203 in BCa tissues, normal adjacent tissues, and BCa cell lines were detected. BCa cells were transfected with miR-203 mimic and inhibitor to investigate the effect of miR-203 on cell functions and the epithelial–mesenchymal transition (EMT). Cotransfection with miR-203 inhibitor and shRNA of the predicted target gene Twist1 (si-Twist1) was performed to investigate the target relationship of miR-203 and Twist1. The effects of knockdown of Twist1 on cell functions were also investigated. The expression of miR-203 was significantly reduced in BCa tissues and cells, in comparison with the control. miR-203 mimic significantly reduced cell viability, invasion, migration, and EMT, and enhanced cell apoptosis. On the contrary, miR-203 inhibitor showed the opposite results. However, the administration of si-Twist1 cancelled the effect of miR-203 inhibitor on cell proliferation, apoptosis, invasion, and migration. These demonstrated that miR-203 may function as a tumor-suppressive microRNA in BCa by negatively targeting Twist1. Both Twist1 and miR-203 might be explored as potential targets for studying the mechanism related to BCa pathogenesis and therapy. Cognizant Communication Corporation 2018-09-14 /pmc/articles/PMC7844766/ /pubmed/28893347 http://dx.doi.org/10.3727/096504017X15041934685237 Text en Copyright © 2018 Cognizant, LLC. http://creativecommons.org/licenses/by-nc-nd/4.0/ This article is licensed under a Creative Commons Attribution-NonCommercial NoDerivatives 4.0 International License. |
spellingShingle | Article Shen, Jie Zhang, Jianhua Xiao, Minhui Yang, Junfeng Zhang, Ningnan miR-203 Suppresses Bladder Cancer Cell Growth and Targets Twist1 |
title | miR-203 Suppresses Bladder Cancer Cell Growth and Targets Twist1 |
title_full | miR-203 Suppresses Bladder Cancer Cell Growth and Targets Twist1 |
title_fullStr | miR-203 Suppresses Bladder Cancer Cell Growth and Targets Twist1 |
title_full_unstemmed | miR-203 Suppresses Bladder Cancer Cell Growth and Targets Twist1 |
title_short | miR-203 Suppresses Bladder Cancer Cell Growth and Targets Twist1 |
title_sort | mir-203 suppresses bladder cancer cell growth and targets twist1 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7844766/ https://www.ncbi.nlm.nih.gov/pubmed/28893347 http://dx.doi.org/10.3727/096504017X15041934685237 |
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