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Prognostic Value of microRNA-9 in Various Cancers: a Meta-analysis

Recently, there are more and more evidences from studies have revealed the association between microRNA-9 (miR-9) expression and outcome in multiple cancers, but inconsistent results have also been reported. It is necessary to rationalize a meta analysis of all available data to clarify the prognost...

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Autores principales: Zhang, Yunyuan, Zhou, Jun, Sun, Meiling, Sun, Guirong, Cao, Yongxian, Zhang, Haiping, Tian, Runhua, Zhou, Lan, Duan, Liang, Chen, Xian, Lun, Limin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Netherlands 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5487937/
https://www.ncbi.nlm.nih.gov/pubmed/27844330
http://dx.doi.org/10.1007/s12253-016-0148-4
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author Zhang, Yunyuan
Zhou, Jun
Sun, Meiling
Sun, Guirong
Cao, Yongxian
Zhang, Haiping
Tian, Runhua
Zhou, Lan
Duan, Liang
Chen, Xian
Lun, Limin
author_facet Zhang, Yunyuan
Zhou, Jun
Sun, Meiling
Sun, Guirong
Cao, Yongxian
Zhang, Haiping
Tian, Runhua
Zhou, Lan
Duan, Liang
Chen, Xian
Lun, Limin
author_sort Zhang, Yunyuan
collection PubMed
description Recently, there are more and more evidences from studies have revealed the association between microRNA-9 (miR-9) expression and outcome in multiple cancers, but inconsistent results have also been reported. It is necessary to rationalize a meta analysis of all available data to clarify the prognostic role of miR-9. Eligible studies were selected through multiple search strategies and the quality was assessed by MOOSE. Data was extracted from studies according to the key statistics index. All analyses were performed using STATA software. Twenty studies were selected in the meta-analysis to evaluate the prognostic role of miR-9 in multiple tumors. MiR-9 expression level was an independent prognostic biomarker for OS in tumor patients using multivariate and univariate analyses. High expression levels of miR-9 was demonstrated to associated with poor overall survival (OS) (HR = 2.23, 95 % CI: 1.56–3.17, P < 0.05) and recurrence free survival/progress free survival (RFS/PFS) (HR = 2.08, 95 % CI: 1.33–3.27, P < 0.05). Subgroup analysis showed that residence region (China and Japan), sample size, cancer type (solid or leukemia), follow-up months and analysis method (qPCR) did not alter the predictive value of miR-9 on OS in various cancers. Furthermore, no significant associations were detected for miR-9 expression and lymph node metastasis or distant metastasis. The present results suggest that promoted miR-9 expression is associated with poor OS in patients with general cancers. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s12253-016-0148-4) contains supplementary material, which is available to authorized users.
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spelling pubmed-54879372017-07-03 Prognostic Value of microRNA-9 in Various Cancers: a Meta-analysis Zhang, Yunyuan Zhou, Jun Sun, Meiling Sun, Guirong Cao, Yongxian Zhang, Haiping Tian, Runhua Zhou, Lan Duan, Liang Chen, Xian Lun, Limin Pathol Oncol Res Original Article Recently, there are more and more evidences from studies have revealed the association between microRNA-9 (miR-9) expression and outcome in multiple cancers, but inconsistent results have also been reported. It is necessary to rationalize a meta analysis of all available data to clarify the prognostic role of miR-9. Eligible studies were selected through multiple search strategies and the quality was assessed by MOOSE. Data was extracted from studies according to the key statistics index. All analyses were performed using STATA software. Twenty studies were selected in the meta-analysis to evaluate the prognostic role of miR-9 in multiple tumors. MiR-9 expression level was an independent prognostic biomarker for OS in tumor patients using multivariate and univariate analyses. High expression levels of miR-9 was demonstrated to associated with poor overall survival (OS) (HR = 2.23, 95 % CI: 1.56–3.17, P < 0.05) and recurrence free survival/progress free survival (RFS/PFS) (HR = 2.08, 95 % CI: 1.33–3.27, P < 0.05). Subgroup analysis showed that residence region (China and Japan), sample size, cancer type (solid or leukemia), follow-up months and analysis method (qPCR) did not alter the predictive value of miR-9 on OS in various cancers. Furthermore, no significant associations were detected for miR-9 expression and lymph node metastasis or distant metastasis. The present results suggest that promoted miR-9 expression is associated with poor OS in patients with general cancers. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s12253-016-0148-4) contains supplementary material, which is available to authorized users. Springer Netherlands 2016-11-14 2017 /pmc/articles/PMC5487937/ /pubmed/27844330 http://dx.doi.org/10.1007/s12253-016-0148-4 Text en © The Author(s) 2016 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/), 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.
spellingShingle Original Article
Zhang, Yunyuan
Zhou, Jun
Sun, Meiling
Sun, Guirong
Cao, Yongxian
Zhang, Haiping
Tian, Runhua
Zhou, Lan
Duan, Liang
Chen, Xian
Lun, Limin
Prognostic Value of microRNA-9 in Various Cancers: a Meta-analysis
title Prognostic Value of microRNA-9 in Various Cancers: a Meta-analysis
title_full Prognostic Value of microRNA-9 in Various Cancers: a Meta-analysis
title_fullStr Prognostic Value of microRNA-9 in Various Cancers: a Meta-analysis
title_full_unstemmed Prognostic Value of microRNA-9 in Various Cancers: a Meta-analysis
title_short Prognostic Value of microRNA-9 in Various Cancers: a Meta-analysis
title_sort prognostic value of microrna-9 in various cancers: a meta-analysis
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5487937/
https://www.ncbi.nlm.nih.gov/pubmed/27844330
http://dx.doi.org/10.1007/s12253-016-0148-4
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