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MiR-486 as an effective biomarker in cancer diagnosis and prognosis: a systematic review and meta-analysis

PURPOSE: MiR-486 was found to be associated with cancer’s diagnosis and prognosis. This meta-analysis aimed to investigate the potential effect of miR-486 on cancer detection and prognosis. MATERIALS AND METHODS: We searched PubMed, Cochrane library, Embase, Chinese National Knowledge Infrastructure...

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Autores principales: Jiang, Min, Li, Xuelian, Quan, Xiaowei, Yang, Xianglin, Zheng, Chang, Hao, Xia, Qu, Ruoyi, Zhou, Baosen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5862628/
https://www.ncbi.nlm.nih.gov/pubmed/29568407
http://dx.doi.org/10.18632/oncotarget.24189
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author Jiang, Min
Li, Xuelian
Quan, Xiaowei
Yang, Xianglin
Zheng, Chang
Hao, Xia
Qu, Ruoyi
Zhou, Baosen
author_facet Jiang, Min
Li, Xuelian
Quan, Xiaowei
Yang, Xianglin
Zheng, Chang
Hao, Xia
Qu, Ruoyi
Zhou, Baosen
author_sort Jiang, Min
collection PubMed
description PURPOSE: MiR-486 was found to be associated with cancer’s diagnosis and prognosis. This meta-analysis aimed to investigate the potential effect of miR-486 on cancer detection and prognosis. MATERIALS AND METHODS: We searched PubMed, Cochrane library, Embase, Chinese National Knowledge Infrastructure (CNKI) and Wanfang databases to find all correlated articles. The STATA 11.0 was applied to estimate the pooled effects, heterogeneity and publication bias. RESULTS: The pooled sensitivity (SEN), specificity (SPE) and Area under the curve (AUC) were 82% (95% CI: 78–85%), 88% (95% CI: 83–92%) and 0.91 (95% CI: 0.88–0.93). Subgroup analysis indicated miR-486 from circulating samples exhibited higher diagnostic accuracy with the AUC was 0.90 (95% CI: 0.87–0.92) than miR-486 from other specimen with the AUC of 0.78 (95% CI: 0.75–0.82) and miR-486 obtained a better diagnostic value in the Asian population with the AUC of 0.94 (95% CI: 0.91–0.95) than the Caucasian and Caucasian/African population with the AUC of 0.80 (95% CI: 0.76–0.83) and 0.89 (95% CI: 0.86–0.91) respectively. MiR-486 obtained high value for the diagnosis of non-small cell lung cancer with SEN, SPE and AUC were 0.82 (95% CI: 0.0.77–0.87), 0.90 (95% CI: 0.84–0.94) as well as 0.92 (95% CI: 0.89–0.94) respectively. For the 7 prognostic tests, the pooled hazard ratio (HR) was 0.48 (95% CI: –0.13–1.08) for low versus high miR-486 expression. CONCLUSIONS: This meta-analysis indicated that miR-486 can be used as ideal biomarkers in the cancer’s diagnosis. However, Low miR-486 expression did not increase the risk of poor outcome.
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spelling pubmed-58626282018-03-22 MiR-486 as an effective biomarker in cancer diagnosis and prognosis: a systematic review and meta-analysis Jiang, Min Li, Xuelian Quan, Xiaowei Yang, Xianglin Zheng, Chang Hao, Xia Qu, Ruoyi Zhou, Baosen Oncotarget Meta-Analysis PURPOSE: MiR-486 was found to be associated with cancer’s diagnosis and prognosis. This meta-analysis aimed to investigate the potential effect of miR-486 on cancer detection and prognosis. MATERIALS AND METHODS: We searched PubMed, Cochrane library, Embase, Chinese National Knowledge Infrastructure (CNKI) and Wanfang databases to find all correlated articles. The STATA 11.0 was applied to estimate the pooled effects, heterogeneity and publication bias. RESULTS: The pooled sensitivity (SEN), specificity (SPE) and Area under the curve (AUC) were 82% (95% CI: 78–85%), 88% (95% CI: 83–92%) and 0.91 (95% CI: 0.88–0.93). Subgroup analysis indicated miR-486 from circulating samples exhibited higher diagnostic accuracy with the AUC was 0.90 (95% CI: 0.87–0.92) than miR-486 from other specimen with the AUC of 0.78 (95% CI: 0.75–0.82) and miR-486 obtained a better diagnostic value in the Asian population with the AUC of 0.94 (95% CI: 0.91–0.95) than the Caucasian and Caucasian/African population with the AUC of 0.80 (95% CI: 0.76–0.83) and 0.89 (95% CI: 0.86–0.91) respectively. MiR-486 obtained high value for the diagnosis of non-small cell lung cancer with SEN, SPE and AUC were 0.82 (95% CI: 0.0.77–0.87), 0.90 (95% CI: 0.84–0.94) as well as 0.92 (95% CI: 0.89–0.94) respectively. For the 7 prognostic tests, the pooled hazard ratio (HR) was 0.48 (95% CI: –0.13–1.08) for low versus high miR-486 expression. CONCLUSIONS: This meta-analysis indicated that miR-486 can be used as ideal biomarkers in the cancer’s diagnosis. However, Low miR-486 expression did not increase the risk of poor outcome. Impact Journals LLC 2018-01-12 /pmc/articles/PMC5862628/ /pubmed/29568407 http://dx.doi.org/10.18632/oncotarget.24189 Text en Copyright: © 2018 Jiang 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
Jiang, Min
Li, Xuelian
Quan, Xiaowei
Yang, Xianglin
Zheng, Chang
Hao, Xia
Qu, Ruoyi
Zhou, Baosen
MiR-486 as an effective biomarker in cancer diagnosis and prognosis: a systematic review and meta-analysis
title MiR-486 as an effective biomarker in cancer diagnosis and prognosis: a systematic review and meta-analysis
title_full MiR-486 as an effective biomarker in cancer diagnosis and prognosis: a systematic review and meta-analysis
title_fullStr MiR-486 as an effective biomarker in cancer diagnosis and prognosis: a systematic review and meta-analysis
title_full_unstemmed MiR-486 as an effective biomarker in cancer diagnosis and prognosis: a systematic review and meta-analysis
title_short MiR-486 as an effective biomarker in cancer diagnosis and prognosis: a systematic review and meta-analysis
title_sort mir-486 as an effective biomarker in cancer diagnosis and prognosis: a systematic review and meta-analysis
topic Meta-Analysis
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5862628/
https://www.ncbi.nlm.nih.gov/pubmed/29568407
http://dx.doi.org/10.18632/oncotarget.24189
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