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MicroRNA-181 as a prognostic biomarker for survival in acute myeloid leukemia: a meta-analysis

Accumulating evidence has indicated that microRNA-181 (miR-181) is dysregulated in hematological malignancies, and associates with the clinical outcomes. However, the association of miR-181 expression levels with acute myeloid leukemia (AML) remains inconclusive, as publications from different group...

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Autores principales: Guo, Qiang, Luan, Junwen, Li, Ni, Zhang, Zhen, Zhu, Xiaoxiao, Zhao, Lin, Wei, Ran, Sun, Linlin, Shi, Yin, Yin, Xunqiang, Ding, Na, Jiang, Guosheng, Li, Xia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5687675/
https://www.ncbi.nlm.nih.gov/pubmed/29179505
http://dx.doi.org/10.18632/oncotarget.19195
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author Guo, Qiang
Luan, Junwen
Li, Ni
Zhang, Zhen
Zhu, Xiaoxiao
Zhao, Lin
Wei, Ran
Sun, Linlin
Shi, Yin
Yin, Xunqiang
Ding, Na
Jiang, Guosheng
Li, Xia
author_facet Guo, Qiang
Luan, Junwen
Li, Ni
Zhang, Zhen
Zhu, Xiaoxiao
Zhao, Lin
Wei, Ran
Sun, Linlin
Shi, Yin
Yin, Xunqiang
Ding, Na
Jiang, Guosheng
Li, Xia
author_sort Guo, Qiang
collection PubMed
description Accumulating evidence has indicated that microRNA-181 (miR-181) is dysregulated in hematological malignancies, and associates with the clinical outcomes. However, the association of miR-181 expression levels with acute myeloid leukemia (AML) remains inconclusive, as publications from different groups have reported contradictory results. In this manuscript, a meta-analysis was performed to assess the prognostic significance of miR-181 in AML patients. Eligible studies were retrieved from PubMed, Embase and Cochrane Library databases, and a total of 6 studies including 815 AML patients were included in the final analysis. Hazard ratios (HRs) and their corresponding 95% confidence intervals (CIs) were extracted and pooled to investigate the correlation between miR-181 and the survival of AML patients. Our results showed that elevated miR-181 expression was associated with increased survival in 395 American patients, and reduced survival in 325 Chinese patients. Both subgroup analyses and meta-regression indicated that the origin of AML patients contributed to the heterogeneity in the datasets evaluating the correlation between overall survival (OS) and miR-181. These results indicate that miR-181 can be used as a promising prognostic biomarker in AML patients, which may depend on the origin of patient population.
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spelling pubmed-56876752017-11-20 MicroRNA-181 as a prognostic biomarker for survival in acute myeloid leukemia: a meta-analysis Guo, Qiang Luan, Junwen Li, Ni Zhang, Zhen Zhu, Xiaoxiao Zhao, Lin Wei, Ran Sun, Linlin Shi, Yin Yin, Xunqiang Ding, Na Jiang, Guosheng Li, Xia Oncotarget Meta-Analysis Accumulating evidence has indicated that microRNA-181 (miR-181) is dysregulated in hematological malignancies, and associates with the clinical outcomes. However, the association of miR-181 expression levels with acute myeloid leukemia (AML) remains inconclusive, as publications from different groups have reported contradictory results. In this manuscript, a meta-analysis was performed to assess the prognostic significance of miR-181 in AML patients. Eligible studies were retrieved from PubMed, Embase and Cochrane Library databases, and a total of 6 studies including 815 AML patients were included in the final analysis. Hazard ratios (HRs) and their corresponding 95% confidence intervals (CIs) were extracted and pooled to investigate the correlation between miR-181 and the survival of AML patients. Our results showed that elevated miR-181 expression was associated with increased survival in 395 American patients, and reduced survival in 325 Chinese patients. Both subgroup analyses and meta-regression indicated that the origin of AML patients contributed to the heterogeneity in the datasets evaluating the correlation between overall survival (OS) and miR-181. These results indicate that miR-181 can be used as a promising prognostic biomarker in AML patients, which may depend on the origin of patient population. Impact Journals LLC 2017-07-12 /pmc/articles/PMC5687675/ /pubmed/29179505 http://dx.doi.org/10.18632/oncotarget.19195 Text en Copyright: © 2017 Guo et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) 3.0 (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Meta-Analysis
Guo, Qiang
Luan, Junwen
Li, Ni
Zhang, Zhen
Zhu, Xiaoxiao
Zhao, Lin
Wei, Ran
Sun, Linlin
Shi, Yin
Yin, Xunqiang
Ding, Na
Jiang, Guosheng
Li, Xia
MicroRNA-181 as a prognostic biomarker for survival in acute myeloid leukemia: a meta-analysis
title MicroRNA-181 as a prognostic biomarker for survival in acute myeloid leukemia: a meta-analysis
title_full MicroRNA-181 as a prognostic biomarker for survival in acute myeloid leukemia: a meta-analysis
title_fullStr MicroRNA-181 as a prognostic biomarker for survival in acute myeloid leukemia: a meta-analysis
title_full_unstemmed MicroRNA-181 as a prognostic biomarker for survival in acute myeloid leukemia: a meta-analysis
title_short MicroRNA-181 as a prognostic biomarker for survival in acute myeloid leukemia: a meta-analysis
title_sort microrna-181 as a prognostic biomarker for survival in acute myeloid leukemia: a meta-analysis
topic Meta-Analysis
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5687675/
https://www.ncbi.nlm.nih.gov/pubmed/29179505
http://dx.doi.org/10.18632/oncotarget.19195
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