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High expression of microRNA 221 is a poor predictor for glioma
BACKGROUND: MicroRNA 221 has been found to be a good marker for several cancers. Some studies also focused on the relationship between microRNA 221 and glioma. However, the results are controversial. We aimed to systematically evaluate the prognostic role of microRNA 221 in glioma through performing...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7717837/ https://www.ncbi.nlm.nih.gov/pubmed/33285691 http://dx.doi.org/10.1097/MD.0000000000023163 |
_version_ | 1783619383082352640 |
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author | Song, Yanlin He, Min Zhang, Jing Xu, Jianguo |
author_facet | Song, Yanlin He, Min Zhang, Jing Xu, Jianguo |
author_sort | Song, Yanlin |
collection | PubMed |
description | BACKGROUND: MicroRNA 221 has been found to be a good marker for several cancers. Some studies also focused on the relationship between microRNA 221 and glioma. However, the results are controversial. We aimed to systematically evaluate the prognostic role of microRNA 221 in glioma through performing a meta-analysis. METHODS: The articles which were included in our study were searched on the Web of Science, EMBASE, PubMed, Cochrane Library and China National Knowledge Infrastructure. The basic characteristics and relevant data were extracted. Hazard ratios (HRs) with 95% confidence intervals (CIs) were pooled to evaluate the prognostic role of microRNA 221 in glioma. RESULTS: Eight studies with 1069 patients were included. We systematically evaluated the role of microRNA 221 for overall survival (OS) and disease free survival (DFS) in glioma patients (HR for OS = 1.66, 95% CI, 1.34–2.04; HR for DFS = 1.14, 95% CI, 1.02–1.26). Subgroup analyses were performed according to the nation of the studies, the origin of the samples, the stage of the tumors, the cut-off value, and the method for detecting the microRNA 221. No significant publication bias was found (P = .133). CONCLUSION: In conclusion, high expression of microRNA 221 was related to poor prognosis of glioma. These findings may assist future exploration on microRNA 221 and help predict the prognosis of glioma. However, due to the significant heterogeneity of these studies, more studies are warranted. |
format | Online Article Text |
id | pubmed-7717837 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-77178372020-12-07 High expression of microRNA 221 is a poor predictor for glioma Song, Yanlin He, Min Zhang, Jing Xu, Jianguo Medicine (Baltimore) 5700 BACKGROUND: MicroRNA 221 has been found to be a good marker for several cancers. Some studies also focused on the relationship between microRNA 221 and glioma. However, the results are controversial. We aimed to systematically evaluate the prognostic role of microRNA 221 in glioma through performing a meta-analysis. METHODS: The articles which were included in our study were searched on the Web of Science, EMBASE, PubMed, Cochrane Library and China National Knowledge Infrastructure. The basic characteristics and relevant data were extracted. Hazard ratios (HRs) with 95% confidence intervals (CIs) were pooled to evaluate the prognostic role of microRNA 221 in glioma. RESULTS: Eight studies with 1069 patients were included. We systematically evaluated the role of microRNA 221 for overall survival (OS) and disease free survival (DFS) in glioma patients (HR for OS = 1.66, 95% CI, 1.34–2.04; HR for DFS = 1.14, 95% CI, 1.02–1.26). Subgroup analyses were performed according to the nation of the studies, the origin of the samples, the stage of the tumors, the cut-off value, and the method for detecting the microRNA 221. No significant publication bias was found (P = .133). CONCLUSION: In conclusion, high expression of microRNA 221 was related to poor prognosis of glioma. These findings may assist future exploration on microRNA 221 and help predict the prognosis of glioma. However, due to the significant heterogeneity of these studies, more studies are warranted. Lippincott Williams & Wilkins 2020-12-04 /pmc/articles/PMC7717837/ /pubmed/33285691 http://dx.doi.org/10.1097/MD.0000000000023163 Text en Copyright © 2020 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by-nc/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial License 4.0 (CCBY-NC), where it is permissible to download, share, remix, transform, and buildup the work provided it is properly cited. The work cannot be used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc/4.0 |
spellingShingle | 5700 Song, Yanlin He, Min Zhang, Jing Xu, Jianguo High expression of microRNA 221 is a poor predictor for glioma |
title | High expression of microRNA 221 is a poor predictor for glioma |
title_full | High expression of microRNA 221 is a poor predictor for glioma |
title_fullStr | High expression of microRNA 221 is a poor predictor for glioma |
title_full_unstemmed | High expression of microRNA 221 is a poor predictor for glioma |
title_short | High expression of microRNA 221 is a poor predictor for glioma |
title_sort | high expression of microrna 221 is a poor predictor for glioma |
topic | 5700 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7717837/ https://www.ncbi.nlm.nih.gov/pubmed/33285691 http://dx.doi.org/10.1097/MD.0000000000023163 |
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