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MicroRNAs with prognostic significance in bladder cancer: a systematic review and meta-analysis

The aim of this study was to systematically review articles that investigated the prognostic significance of different microRNAs in bladder cancer (BC). We systematically searched PubMed, Web of Science, and Embase to identify relevant studies until March 2016. After screening, 26 studies that invol...

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Autores principales: Xie, Yongpeng, Ma, Xin, Chen, Luyao, Li, Hongzhao, Gu, Liangyou, Gao, Yu, Zhang, Yu, Li, Xintao, Fan, Yang, Chen, Jianwen, Zhang, Xu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5514092/
https://www.ncbi.nlm.nih.gov/pubmed/28717125
http://dx.doi.org/10.1038/s41598-017-05801-3
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author Xie, Yongpeng
Ma, Xin
Chen, Luyao
Li, Hongzhao
Gu, Liangyou
Gao, Yu
Zhang, Yu
Li, Xintao
Fan, Yang
Chen, Jianwen
Zhang, Xu
author_facet Xie, Yongpeng
Ma, Xin
Chen, Luyao
Li, Hongzhao
Gu, Liangyou
Gao, Yu
Zhang, Yu
Li, Xintao
Fan, Yang
Chen, Jianwen
Zhang, Xu
author_sort Xie, Yongpeng
collection PubMed
description The aim of this study was to systematically review articles that investigated the prognostic significance of different microRNAs in bladder cancer (BC). We systematically searched PubMed, Web of Science, and Embase to identify relevant studies until March 2016. After screening, 26 studies that involved 2753 patients were included. Results suggested that many miRs expression aberration may predict prognosis in patients with BC. There are six miRs (miR-21, miR-143, miR-155, miR-200, miR-214, and miR-222) were reported by at least two studies, and we performed meta-analysis in the corresponding studies. Accordingly, we found that high miR-21 expression was associated with poor overall survival [OS; hazard ratio (HR) = 3.94, 95% CI 2.08–7.44]. High miR-143 expression was associated with poor progression-free survival (PFS; HR = 3.78, 95% CI 1.61–8.89). High miR-155 expression was associated with poor PFS (HR = 8.10, 95% CI 2.92–22.48). High miR-222 expression was associated with poor OS (HR = 3.39, 95% CI 1.10–10.41). Meanwhile, low miR-214 expression was correlated with poor RFS(HR = 0.34, 95% CI 0.22–0.53). Our comprehensive systematic review concluded that microRNAs, particularly miR-21, miR-143, miR-155, miR-214, and miR-222, could serve as meticulous follow-up markers for early detection of progression or recurrence and even useful therapeutic targets for the treatment in patients with BC.
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spelling pubmed-55140922017-07-19 MicroRNAs with prognostic significance in bladder cancer: a systematic review and meta-analysis Xie, Yongpeng Ma, Xin Chen, Luyao Li, Hongzhao Gu, Liangyou Gao, Yu Zhang, Yu Li, Xintao Fan, Yang Chen, Jianwen Zhang, Xu Sci Rep Article The aim of this study was to systematically review articles that investigated the prognostic significance of different microRNAs in bladder cancer (BC). We systematically searched PubMed, Web of Science, and Embase to identify relevant studies until March 2016. After screening, 26 studies that involved 2753 patients were included. Results suggested that many miRs expression aberration may predict prognosis in patients with BC. There are six miRs (miR-21, miR-143, miR-155, miR-200, miR-214, and miR-222) were reported by at least two studies, and we performed meta-analysis in the corresponding studies. Accordingly, we found that high miR-21 expression was associated with poor overall survival [OS; hazard ratio (HR) = 3.94, 95% CI 2.08–7.44]. High miR-143 expression was associated with poor progression-free survival (PFS; HR = 3.78, 95% CI 1.61–8.89). High miR-155 expression was associated with poor PFS (HR = 8.10, 95% CI 2.92–22.48). High miR-222 expression was associated with poor OS (HR = 3.39, 95% CI 1.10–10.41). Meanwhile, low miR-214 expression was correlated with poor RFS(HR = 0.34, 95% CI 0.22–0.53). Our comprehensive systematic review concluded that microRNAs, particularly miR-21, miR-143, miR-155, miR-214, and miR-222, could serve as meticulous follow-up markers for early detection of progression or recurrence and even useful therapeutic targets for the treatment in patients with BC. Nature Publishing Group UK 2017-07-17 /pmc/articles/PMC5514092/ /pubmed/28717125 http://dx.doi.org/10.1038/s41598-017-05801-3 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Xie, Yongpeng
Ma, Xin
Chen, Luyao
Li, Hongzhao
Gu, Liangyou
Gao, Yu
Zhang, Yu
Li, Xintao
Fan, Yang
Chen, Jianwen
Zhang, Xu
MicroRNAs with prognostic significance in bladder cancer: a systematic review and meta-analysis
title MicroRNAs with prognostic significance in bladder cancer: a systematic review and meta-analysis
title_full MicroRNAs with prognostic significance in bladder cancer: a systematic review and meta-analysis
title_fullStr MicroRNAs with prognostic significance in bladder cancer: a systematic review and meta-analysis
title_full_unstemmed MicroRNAs with prognostic significance in bladder cancer: a systematic review and meta-analysis
title_short MicroRNAs with prognostic significance in bladder cancer: a systematic review and meta-analysis
title_sort micrornas with prognostic significance in bladder cancer: a systematic review and meta-analysis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5514092/
https://www.ncbi.nlm.nih.gov/pubmed/28717125
http://dx.doi.org/10.1038/s41598-017-05801-3
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