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Prognostic role of miR-9 expression in various human malignant neoplasms: a meta-analysis

Emerging evidence has shown that aberrant microRNA expression has the potential to be used for predicting survival and treatment response of malignant neoplasms. In recent years, the role of miR-9 had been investigated in various types of cancers, and it was found that the results were inconsistent...

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Autores principales: Liu, Xiaodan, Luo, Ziyan, Peng, Hongxia, Jiang, Hua, Xu, Ling
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4883817/
https://www.ncbi.nlm.nih.gov/pubmed/27284255
http://dx.doi.org/10.2147/OTT.S98923
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author Liu, Xiaodan
Luo, Ziyan
Peng, Hongxia
Jiang, Hua
Xu, Ling
author_facet Liu, Xiaodan
Luo, Ziyan
Peng, Hongxia
Jiang, Hua
Xu, Ling
author_sort Liu, Xiaodan
collection PubMed
description Emerging evidence has shown that aberrant microRNA expression has the potential to be used for predicting survival and treatment response of malignant neoplasms. In recent years, the role of miR-9 had been investigated in various types of cancers, and it was found that the results were inconsistent and inconclusive. Hence, in this study, a meta-analysis was conducted to assess the prognostic value of miR-9 in various types of tumors. Eligible studies were identified through a systematic search in PubMed and EMBASE and then were assessed by further quality evaluation. Pooled hazard ratios (HRs) with 95% confidence intervals for overall survival (OS) were calculated to investigate the association between miR-9 expression and cancer prognosis. The pooled results of eight published studies showed that elevated miR-9 was a predictor of poor survival of various carcinomas, with pooled HR of 3.04 (95% confidence interval: 1.96–4.73) for OS. Subgroup analysis on the basis of tumor type, sample size, and HR estimate also showed that high levels of miR-9 were also significantly correlated with OS. In addition, when the subgroup analyses were grouped by follow-up time, it was found that the elevated expression of miR-9 was associated with a lower long-term survival when the follow-up time was >60 months, but there was no correlation between the outcomes and those patients whose follow-up time was <60 months. Funnel plots and Egger’s tests revealed that there was no obvious publication bias risk in the meta-analysis. In conclusion, our results demonstrated that higher expression level of miR-9 significantly predicted worse OS in various carcinomas and that miR-9 may act as a novel biomarker in the prognosis of malignant neoplasms.
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spelling pubmed-48838172016-06-09 Prognostic role of miR-9 expression in various human malignant neoplasms: a meta-analysis Liu, Xiaodan Luo, Ziyan Peng, Hongxia Jiang, Hua Xu, Ling Onco Targets Ther Review Emerging evidence has shown that aberrant microRNA expression has the potential to be used for predicting survival and treatment response of malignant neoplasms. In recent years, the role of miR-9 had been investigated in various types of cancers, and it was found that the results were inconsistent and inconclusive. Hence, in this study, a meta-analysis was conducted to assess the prognostic value of miR-9 in various types of tumors. Eligible studies were identified through a systematic search in PubMed and EMBASE and then were assessed by further quality evaluation. Pooled hazard ratios (HRs) with 95% confidence intervals for overall survival (OS) were calculated to investigate the association between miR-9 expression and cancer prognosis. The pooled results of eight published studies showed that elevated miR-9 was a predictor of poor survival of various carcinomas, with pooled HR of 3.04 (95% confidence interval: 1.96–4.73) for OS. Subgroup analysis on the basis of tumor type, sample size, and HR estimate also showed that high levels of miR-9 were also significantly correlated with OS. In addition, when the subgroup analyses were grouped by follow-up time, it was found that the elevated expression of miR-9 was associated with a lower long-term survival when the follow-up time was >60 months, but there was no correlation between the outcomes and those patients whose follow-up time was <60 months. Funnel plots and Egger’s tests revealed that there was no obvious publication bias risk in the meta-analysis. In conclusion, our results demonstrated that higher expression level of miR-9 significantly predicted worse OS in various carcinomas and that miR-9 may act as a novel biomarker in the prognosis of malignant neoplasms. Dove Medical Press 2016-05-23 /pmc/articles/PMC4883817/ /pubmed/27284255 http://dx.doi.org/10.2147/OTT.S98923 Text en © 2016 Liu et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Review
Liu, Xiaodan
Luo, Ziyan
Peng, Hongxia
Jiang, Hua
Xu, Ling
Prognostic role of miR-9 expression in various human malignant neoplasms: a meta-analysis
title Prognostic role of miR-9 expression in various human malignant neoplasms: a meta-analysis
title_full Prognostic role of miR-9 expression in various human malignant neoplasms: a meta-analysis
title_fullStr Prognostic role of miR-9 expression in various human malignant neoplasms: a meta-analysis
title_full_unstemmed Prognostic role of miR-9 expression in various human malignant neoplasms: a meta-analysis
title_short Prognostic role of miR-9 expression in various human malignant neoplasms: a meta-analysis
title_sort prognostic role of mir-9 expression in various human malignant neoplasms: a meta-analysis
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4883817/
https://www.ncbi.nlm.nih.gov/pubmed/27284255
http://dx.doi.org/10.2147/OTT.S98923
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