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The prognostic value of decreased miR-101 in various cancers: a meta-analysis of 12 studies

BACKGROUND: A consensus regarding the prognostic value of decreased miR-101 in human cancers has not been reached. This study aimed to comprehensively investigate the internal associations between loss of miR-101 expression and prognostic implications in patients with cancer. MATERIALS AND METHODS:...

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Autores principales: Hu, Jianpei, Wu, Chunyu, Zhao, Xueying, Liu, Chaodong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5533486/
https://www.ncbi.nlm.nih.gov/pubmed/28769574
http://dx.doi.org/10.2147/OTT.S141652
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author Hu, Jianpei
Wu, Chunyu
Zhao, Xueying
Liu, Chaodong
author_facet Hu, Jianpei
Wu, Chunyu
Zhao, Xueying
Liu, Chaodong
author_sort Hu, Jianpei
collection PubMed
description BACKGROUND: A consensus regarding the prognostic value of decreased miR-101 in human cancers has not been reached. This study aimed to comprehensively investigate the internal associations between loss of miR-101 expression and prognostic implications in patients with cancer. MATERIALS AND METHODS: All relevant literature in electronic databases, including PubMed, ISI Web of Science, and Embase, up to March 1, 2017 were searched. Correlations between decreased miR-101 and clinicopathological parameters were defined by odds ratios (ORs). The degree of association between reduced miR-101 and survival outcome was evaluated by pooled hazard ratios (HRs) and relevant 95% CIs. RESULTS: Twelve eligible studies with 2,088 patients were included in this meta-analysis. Decreased miR-101 expression was closely connected with poor overall survival, with a pooled HR of 2.15 (95% CI 1.71–2.7, P<0.001). This correlation was also revealed when stratified analysis was conducted with respect to ethnicity, cancer type, sample size, specimen source, and analysis model. However, decreased miR-101 was not associated with disease-free survival, recurrence-free survival, or progression-free survival, with a pooled HR of 1.59 (95% CI 0.83–3.03, P=0.128), despite a positive trend. In addition, reduced miR-101 was intimately related to poorer tumor differentiation (OR 2.17, 95% CI 1.14–4.13; P=0.019), advanced tumor classification (OR 5.25, 95% CI 3.39–8.12; P<0.001), and higher TNM stage (OR 6.18, 95% CI 3.79–10.09; P<0.001). CONCLUSION: Our findings suggest that loss of miR-101 expression is correlated with worse overall survival in a variety of cancers, and could serve as a predictive indicator for clinicopathological features. Furthermore, miR-101 may become a feasible therapeutic target in most human cancers.
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spelling pubmed-55334862017-08-02 The prognostic value of decreased miR-101 in various cancers: a meta-analysis of 12 studies Hu, Jianpei Wu, Chunyu Zhao, Xueying Liu, Chaodong Onco Targets Ther Original Research BACKGROUND: A consensus regarding the prognostic value of decreased miR-101 in human cancers has not been reached. This study aimed to comprehensively investigate the internal associations between loss of miR-101 expression and prognostic implications in patients with cancer. MATERIALS AND METHODS: All relevant literature in electronic databases, including PubMed, ISI Web of Science, and Embase, up to March 1, 2017 were searched. Correlations between decreased miR-101 and clinicopathological parameters were defined by odds ratios (ORs). The degree of association between reduced miR-101 and survival outcome was evaluated by pooled hazard ratios (HRs) and relevant 95% CIs. RESULTS: Twelve eligible studies with 2,088 patients were included in this meta-analysis. Decreased miR-101 expression was closely connected with poor overall survival, with a pooled HR of 2.15 (95% CI 1.71–2.7, P<0.001). This correlation was also revealed when stratified analysis was conducted with respect to ethnicity, cancer type, sample size, specimen source, and analysis model. However, decreased miR-101 was not associated with disease-free survival, recurrence-free survival, or progression-free survival, with a pooled HR of 1.59 (95% CI 0.83–3.03, P=0.128), despite a positive trend. In addition, reduced miR-101 was intimately related to poorer tumor differentiation (OR 2.17, 95% CI 1.14–4.13; P=0.019), advanced tumor classification (OR 5.25, 95% CI 3.39–8.12; P<0.001), and higher TNM stage (OR 6.18, 95% CI 3.79–10.09; P<0.001). CONCLUSION: Our findings suggest that loss of miR-101 expression is correlated with worse overall survival in a variety of cancers, and could serve as a predictive indicator for clinicopathological features. Furthermore, miR-101 may become a feasible therapeutic target in most human cancers. Dove Medical Press 2017-07-24 /pmc/articles/PMC5533486/ /pubmed/28769574 http://dx.doi.org/10.2147/OTT.S141652 Text en © 2017 Hu 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 Original Research
Hu, Jianpei
Wu, Chunyu
Zhao, Xueying
Liu, Chaodong
The prognostic value of decreased miR-101 in various cancers: a meta-analysis of 12 studies
title The prognostic value of decreased miR-101 in various cancers: a meta-analysis of 12 studies
title_full The prognostic value of decreased miR-101 in various cancers: a meta-analysis of 12 studies
title_fullStr The prognostic value of decreased miR-101 in various cancers: a meta-analysis of 12 studies
title_full_unstemmed The prognostic value of decreased miR-101 in various cancers: a meta-analysis of 12 studies
title_short The prognostic value of decreased miR-101 in various cancers: a meta-analysis of 12 studies
title_sort prognostic value of decreased mir-101 in various cancers: a meta-analysis of 12 studies
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5533486/
https://www.ncbi.nlm.nih.gov/pubmed/28769574
http://dx.doi.org/10.2147/OTT.S141652
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