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Survival advantage and clinicopathological significance of microRNA-22 in cancers: a meta-analysis

An increasing number of studies revealed that microRNA-22 as a biomarker may play a significant role in the cancer patients’ prognosis, but the accurate prognosis value of microRNA-22 remains somewhat controversial. Thus, we comprehensively searched the database and performed this study to explicate...

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Autores principales: Xiang, Qingming, Xiang, Zhenxian, Dou, Rongzhang, Xiong, Bin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6790216/
https://www.ncbi.nlm.nih.gov/pubmed/31632145
http://dx.doi.org/10.2147/CMAR.S185124
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author Xiang, Qingming
Xiang, Zhenxian
Dou, Rongzhang
Xiong, Bin
author_facet Xiang, Qingming
Xiang, Zhenxian
Dou, Rongzhang
Xiong, Bin
author_sort Xiang, Qingming
collection PubMed
description An increasing number of studies revealed that microRNA-22 as a biomarker may play a significant role in the cancer patients’ prognosis, but the accurate prognosis value of microRNA-22 remains somewhat controversial. Thus, we comprehensively searched the database and performed this study to explicate the accurate value of microRNA-22 in the cancer patients’ prognosis. This meta-analysis revealed that elevated expression of microRNA-22 correlated with good overall survival (OS) and disease-free survival (DFS)/progression-free survival (PFS)/recurrence-free survival (RFS) in cancers, while no significant association was found in metastasis-free survival (MFS)/distant metastasis-free survival (DMFS). Through the subgroup analysis for OS and DFS/PFS/RFS, we found that elevated expression of miR-22 significantly correlated with good prognosis in most subgroups, while it predicted a worse prognosis in nasopharyngeal carcinoma subgroup. And besides that, elevated expression of miR-22 was negatively correlated with TNM stage, lymph node metastasis, distant metastasis and recurrence, while no significant association was found between microRNA-22 expression and T stage, tumor differentiation, and lymphatic invasion. Our meta-analysis demonstrated that elevated expression of microRNA-22 predicted a good OS and DFS/PFS/RFS in cancer patients; meanwhile, its high expression also means earlier TNM stage, and lower likelihoods of lymph node metastasis, of distant metastasis and of recurrence. If we regularly monitor miR-22 expression in cancer patients, it might be useful for us to predict cancer prognosis in future clinical applications.
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spelling pubmed-67902162019-10-18 Survival advantage and clinicopathological significance of microRNA-22 in cancers: a meta-analysis Xiang, Qingming Xiang, Zhenxian Dou, Rongzhang Xiong, Bin Cancer Manag Res Review An increasing number of studies revealed that microRNA-22 as a biomarker may play a significant role in the cancer patients’ prognosis, but the accurate prognosis value of microRNA-22 remains somewhat controversial. Thus, we comprehensively searched the database and performed this study to explicate the accurate value of microRNA-22 in the cancer patients’ prognosis. This meta-analysis revealed that elevated expression of microRNA-22 correlated with good overall survival (OS) and disease-free survival (DFS)/progression-free survival (PFS)/recurrence-free survival (RFS) in cancers, while no significant association was found in metastasis-free survival (MFS)/distant metastasis-free survival (DMFS). Through the subgroup analysis for OS and DFS/PFS/RFS, we found that elevated expression of miR-22 significantly correlated with good prognosis in most subgroups, while it predicted a worse prognosis in nasopharyngeal carcinoma subgroup. And besides that, elevated expression of miR-22 was negatively correlated with TNM stage, lymph node metastasis, distant metastasis and recurrence, while no significant association was found between microRNA-22 expression and T stage, tumor differentiation, and lymphatic invasion. Our meta-analysis demonstrated that elevated expression of microRNA-22 predicted a good OS and DFS/PFS/RFS in cancer patients; meanwhile, its high expression also means earlier TNM stage, and lower likelihoods of lymph node metastasis, of distant metastasis and of recurrence. If we regularly monitor miR-22 expression in cancer patients, it might be useful for us to predict cancer prognosis in future clinical applications. Dove 2019-10-08 /pmc/articles/PMC6790216/ /pubmed/31632145 http://dx.doi.org/10.2147/CMAR.S185124 Text en © 2019 Xiang et al. http://creativecommons.org/licenses/by-nc/3.0/ 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. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Review
Xiang, Qingming
Xiang, Zhenxian
Dou, Rongzhang
Xiong, Bin
Survival advantage and clinicopathological significance of microRNA-22 in cancers: a meta-analysis
title Survival advantage and clinicopathological significance of microRNA-22 in cancers: a meta-analysis
title_full Survival advantage and clinicopathological significance of microRNA-22 in cancers: a meta-analysis
title_fullStr Survival advantage and clinicopathological significance of microRNA-22 in cancers: a meta-analysis
title_full_unstemmed Survival advantage and clinicopathological significance of microRNA-22 in cancers: a meta-analysis
title_short Survival advantage and clinicopathological significance of microRNA-22 in cancers: a meta-analysis
title_sort survival advantage and clinicopathological significance of microrna-22 in cancers: a meta-analysis
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6790216/
https://www.ncbi.nlm.nih.gov/pubmed/31632145
http://dx.doi.org/10.2147/CMAR.S185124
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