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MicroRNA-490-5p is a novel tumor suppressor targeting c-FOS in human bladder cancer
INTRODUCTION: Recent studies have demonstrated the critical roles of micro-RNAs in tumorigenesis and tumor progression. Here, we describe the regulation and function of miR-490-5p in bladder cancer. MATERIAL AND METHODS: Paired tissue samples were collected from bladder cancer patients (n = 20). Rea...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Termedia Publishing House
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4495152/ https://www.ncbi.nlm.nih.gov/pubmed/26170849 http://dx.doi.org/10.5114/aoms.2015.52359 |
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author | Lan, Gongbin Yang, Luoyan Xie, Xubiao Peng, Longkai Wang, Yi |
author_facet | Lan, Gongbin Yang, Luoyan Xie, Xubiao Peng, Longkai Wang, Yi |
author_sort | Lan, Gongbin |
collection | PubMed |
description | INTRODUCTION: Recent studies have demonstrated the critical roles of micro-RNAs in tumorigenesis and tumor progression. Here, we describe the regulation and function of miR-490-5p in bladder cancer. MATERIAL AND METHODS: Paired tissue samples were collected from bladder cancer patients (n = 20). Real-time PCR revealed that miR-490-5p expression was significantly down-regulated in human bladder cancer tissues and cells. Also there was an inverse relationship between the expression level of miR-490-5p and the pathological grade of bladder cancer. Western blotting was performed to detect the expression levels of c-FOS and TET1 in 6 matched tumor tissue samples and 4 bladder cell lines. Furthermore, to better understand the underlying mechanisms of miR-490-5p, we conducted gain and loss of function analysis by transfecting bladder cancer T24 cells with chemically synthesized miR-490-5p mimics and inhibitor, respectively. RESULTS: We found that overexpression of miR-490-5p in T24 cells could inhibit cell proliferation and invasion and induce cell apoptosis. Conversely, suppression of miR-490-5p expression induced cell proliferation and invasion, while it inhibited cell apoptosis. In addition, our bioinformatics prediction and experimental data showed that c-FOS was a potential target of miR-490-5p. The expression level of c-FOS was significantly decreased after miR-490-5p overexpression and significantly increased after miR-490-5p suppression, indicating that c-FOS was a target of miR-490-5p. CONCLUSIONS: These findings suggest that miR-490-5p is a novel tumor suppressor, contributing to the carcinogenesis of bladder cancer by targeting c-FOS. |
format | Online Article Text |
id | pubmed-4495152 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Termedia Publishing House |
record_format | MEDLINE/PubMed |
spelling | pubmed-44951522015-07-13 MicroRNA-490-5p is a novel tumor suppressor targeting c-FOS in human bladder cancer Lan, Gongbin Yang, Luoyan Xie, Xubiao Peng, Longkai Wang, Yi Arch Med Sci Clinical Research INTRODUCTION: Recent studies have demonstrated the critical roles of micro-RNAs in tumorigenesis and tumor progression. Here, we describe the regulation and function of miR-490-5p in bladder cancer. MATERIAL AND METHODS: Paired tissue samples were collected from bladder cancer patients (n = 20). Real-time PCR revealed that miR-490-5p expression was significantly down-regulated in human bladder cancer tissues and cells. Also there was an inverse relationship between the expression level of miR-490-5p and the pathological grade of bladder cancer. Western blotting was performed to detect the expression levels of c-FOS and TET1 in 6 matched tumor tissue samples and 4 bladder cell lines. Furthermore, to better understand the underlying mechanisms of miR-490-5p, we conducted gain and loss of function analysis by transfecting bladder cancer T24 cells with chemically synthesized miR-490-5p mimics and inhibitor, respectively. RESULTS: We found that overexpression of miR-490-5p in T24 cells could inhibit cell proliferation and invasion and induce cell apoptosis. Conversely, suppression of miR-490-5p expression induced cell proliferation and invasion, while it inhibited cell apoptosis. In addition, our bioinformatics prediction and experimental data showed that c-FOS was a potential target of miR-490-5p. The expression level of c-FOS was significantly decreased after miR-490-5p overexpression and significantly increased after miR-490-5p suppression, indicating that c-FOS was a target of miR-490-5p. CONCLUSIONS: These findings suggest that miR-490-5p is a novel tumor suppressor, contributing to the carcinogenesis of bladder cancer by targeting c-FOS. Termedia Publishing House 2015-06-19 2015-06-19 /pmc/articles/PMC4495152/ /pubmed/26170849 http://dx.doi.org/10.5114/aoms.2015.52359 Text en Copyright © 2015 Termedia & Banach http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-Noncommercial 3.0 Unported License, permitting all non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Clinical Research Lan, Gongbin Yang, Luoyan Xie, Xubiao Peng, Longkai Wang, Yi MicroRNA-490-5p is a novel tumor suppressor targeting c-FOS in human bladder cancer |
title | MicroRNA-490-5p is a novel tumor suppressor targeting c-FOS in human bladder cancer |
title_full | MicroRNA-490-5p is a novel tumor suppressor targeting c-FOS in human bladder cancer |
title_fullStr | MicroRNA-490-5p is a novel tumor suppressor targeting c-FOS in human bladder cancer |
title_full_unstemmed | MicroRNA-490-5p is a novel tumor suppressor targeting c-FOS in human bladder cancer |
title_short | MicroRNA-490-5p is a novel tumor suppressor targeting c-FOS in human bladder cancer |
title_sort | microrna-490-5p is a novel tumor suppressor targeting c-fos in human bladder cancer |
topic | Clinical Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4495152/ https://www.ncbi.nlm.nih.gov/pubmed/26170849 http://dx.doi.org/10.5114/aoms.2015.52359 |
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