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Prognostic significance of low microRNA-218 expression in patients with different types of cancer: Evidence from published studies
BACKGROUND: Mounting evidence showed that microRNAs may be useful as prognostic biomarkers of cancer. Therefore, we summarize the predictive role of microRNA-218 (miR-218) for survival in patients with various cancers. METHODS: We performed a systematic literature review and assessed the quality of...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5402571/ https://www.ncbi.nlm.nih.gov/pubmed/27631228 http://dx.doi.org/10.1097/MD.0000000000004773 |
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author | Duan, Fujiao Wang, Kaijuan Dai, Liping Zhao, Xia Feng, Yajing Song, Chunhua Cui, Shuli Wang, Chengzeng |
author_facet | Duan, Fujiao Wang, Kaijuan Dai, Liping Zhao, Xia Feng, Yajing Song, Chunhua Cui, Shuli Wang, Chengzeng |
author_sort | Duan, Fujiao |
collection | PubMed |
description | BACKGROUND: Mounting evidence showed that microRNAs may be useful as prognostic biomarkers of cancer. Therefore, we summarize the predictive role of microRNA-218 (miR-218) for survival in patients with various cancers. METHODS: We performed a systematic literature review and assessed the quality of included studies based on Meta-analysis of Observational Studies in Epidemiology group (MOOSE). Hazard ratios (HRs) with corresponding 95% confidence intervals (CIs) were calculated to assess the correlation between miR-218 expression and prognosis of different cancers. RESULTS: We identified 10 studies for pooled analyses. For overall survival, a lower expression levels of miR-218 significantly predicted poorer survival, with the pooled HR of 2.61 (95% CI: 2.11–3.22, P < 0.001). For disease-free survival/progressive-free survival/recurrence-free survival (DFS/PFS/RFS), a lower expression level of miR-218 significantly predicted worse DFS/PFS/RFS in various carcinomas, with the pooled HR of 2.73 (95% CI: 2.08–3.58, P < 0.001). Similarly, subgroup analysis by detection method, ethnicity and cancer subtype analysis suggested that lower expression of miR-218 correlated with. CONCLUSION: Our data demonstrated that lower miR-218 expression is significantly associated with poorer overall survival (OS) and DFS/PFS/RFS and may be a novel prognostic biomarker in some cancer types. |
format | Online Article Text |
id | pubmed-5402571 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-54025712017-04-27 Prognostic significance of low microRNA-218 expression in patients with different types of cancer: Evidence from published studies Duan, Fujiao Wang, Kaijuan Dai, Liping Zhao, Xia Feng, Yajing Song, Chunhua Cui, Shuli Wang, Chengzeng Medicine (Baltimore) 4400 BACKGROUND: Mounting evidence showed that microRNAs may be useful as prognostic biomarkers of cancer. Therefore, we summarize the predictive role of microRNA-218 (miR-218) for survival in patients with various cancers. METHODS: We performed a systematic literature review and assessed the quality of included studies based on Meta-analysis of Observational Studies in Epidemiology group (MOOSE). Hazard ratios (HRs) with corresponding 95% confidence intervals (CIs) were calculated to assess the correlation between miR-218 expression and prognosis of different cancers. RESULTS: We identified 10 studies for pooled analyses. For overall survival, a lower expression levels of miR-218 significantly predicted poorer survival, with the pooled HR of 2.61 (95% CI: 2.11–3.22, P < 0.001). For disease-free survival/progressive-free survival/recurrence-free survival (DFS/PFS/RFS), a lower expression level of miR-218 significantly predicted worse DFS/PFS/RFS in various carcinomas, with the pooled HR of 2.73 (95% CI: 2.08–3.58, P < 0.001). Similarly, subgroup analysis by detection method, ethnicity and cancer subtype analysis suggested that lower expression of miR-218 correlated with. CONCLUSION: Our data demonstrated that lower miR-218 expression is significantly associated with poorer overall survival (OS) and DFS/PFS/RFS and may be a novel prognostic biomarker in some cancer types. Wolters Kluwer Health 2016-09-16 /pmc/articles/PMC5402571/ /pubmed/27631228 http://dx.doi.org/10.1097/MD.0000000000004773 Text en Copyright © 2016 the Author(s). Published by Wolters Kluwer Health, Inc. All rights reserved. http://creativecommons.org/licenses/by/4.0 This is an open access article distributed under the Creative Commons Attribution License 4.0, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/4.0 |
spellingShingle | 4400 Duan, Fujiao Wang, Kaijuan Dai, Liping Zhao, Xia Feng, Yajing Song, Chunhua Cui, Shuli Wang, Chengzeng Prognostic significance of low microRNA-218 expression in patients with different types of cancer: Evidence from published studies |
title | Prognostic significance of low microRNA-218 expression in patients with different types of cancer: Evidence from published studies |
title_full | Prognostic significance of low microRNA-218 expression in patients with different types of cancer: Evidence from published studies |
title_fullStr | Prognostic significance of low microRNA-218 expression in patients with different types of cancer: Evidence from published studies |
title_full_unstemmed | Prognostic significance of low microRNA-218 expression in patients with different types of cancer: Evidence from published studies |
title_short | Prognostic significance of low microRNA-218 expression in patients with different types of cancer: Evidence from published studies |
title_sort | prognostic significance of low microrna-218 expression in patients with different types of cancer: evidence from published studies |
topic | 4400 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5402571/ https://www.ncbi.nlm.nih.gov/pubmed/27631228 http://dx.doi.org/10.1097/MD.0000000000004773 |
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