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MicroRNA-21 as a potential biomarker for detecting esophageal carcinoma in Asian populations: a meta-analysis
BACKGROUND: MicroRNA-21 (miR-21) is significantly expressed in a variety of cancers and could be used as a tumor biomarker. However, the results are varied, and no studies on the diagnostic usefulness of miR-21 in Asian esophageal cancer (EC) patients have been published. This meta-analysis was aime...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
PeerJ Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9528905/ https://www.ncbi.nlm.nih.gov/pubmed/36199284 http://dx.doi.org/10.7717/peerj.14048 |
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author | Han, Zheng Pan, Lingbo Lu, Bangjie Zhu, Huixia |
author_facet | Han, Zheng Pan, Lingbo Lu, Bangjie Zhu, Huixia |
author_sort | Han, Zheng |
collection | PubMed |
description | BACKGROUND: MicroRNA-21 (miR-21) is significantly expressed in a variety of cancers and could be used as a tumor biomarker. However, the results are varied, and no studies on the diagnostic usefulness of miR-21 in Asian esophageal cancer (EC) patients have been published. This meta-analysis was aimed at exploring whether miR-21 can be used as a diagnostic marker and assessing its effectiveness. METHODS: The relevant literature was identified in six main databases: Ovid MEDLINE, PsycINFO, PubMed MEDLINE, Embase, Web of Science, and the Cochrane Library. Two researchers independently selected the literature based on the inclusion and exclusion criteria, extracted data, and evaluated the risk of bias. The meta-analysis was carried out using Review Manager 5.4, Meta-Disc 1.4 and STATA 15.1 software. In the end, 987 patients from 12 different studies were included. Quality evaluation of diagnostic accuracy studies 2 (QUADAS—2) was used to examine the risk of bias. RESULTS: The pooled sensitivity (SEN) was 0.72 (95% CI [0.69–0.75]), the pooled specificity (SPE) was 0.78 (95% CI [0.75–0.81]), the pooled positive likelihood ratio (PLR) was 2.87 (95% CI [2.28–3.59]), the pooled negative likelihood ratio (NLR) was 0.36 (95% CI [0.31–0.43]), the pooled diagnostic odds ratio (DOR) was 10.00 (95% CI [7.73–12.95]), and the area under the curve 0.82 (95% CI [0.79–0.85]). A Deeks’ funnel plot shows that there was no publication bias (P = 0.99). CONCLUSION: Our findings suggest miR-21 might be the potential biomarker for detecting EC in Asian populations, with a good diagnostic value. |
format | Online Article Text |
id | pubmed-9528905 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | PeerJ Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-95289052022-10-04 MicroRNA-21 as a potential biomarker for detecting esophageal carcinoma in Asian populations: a meta-analysis Han, Zheng Pan, Lingbo Lu, Bangjie Zhu, Huixia PeerJ Molecular Biology BACKGROUND: MicroRNA-21 (miR-21) is significantly expressed in a variety of cancers and could be used as a tumor biomarker. However, the results are varied, and no studies on the diagnostic usefulness of miR-21 in Asian esophageal cancer (EC) patients have been published. This meta-analysis was aimed at exploring whether miR-21 can be used as a diagnostic marker and assessing its effectiveness. METHODS: The relevant literature was identified in six main databases: Ovid MEDLINE, PsycINFO, PubMed MEDLINE, Embase, Web of Science, and the Cochrane Library. Two researchers independently selected the literature based on the inclusion and exclusion criteria, extracted data, and evaluated the risk of bias. The meta-analysis was carried out using Review Manager 5.4, Meta-Disc 1.4 and STATA 15.1 software. In the end, 987 patients from 12 different studies were included. Quality evaluation of diagnostic accuracy studies 2 (QUADAS—2) was used to examine the risk of bias. RESULTS: The pooled sensitivity (SEN) was 0.72 (95% CI [0.69–0.75]), the pooled specificity (SPE) was 0.78 (95% CI [0.75–0.81]), the pooled positive likelihood ratio (PLR) was 2.87 (95% CI [2.28–3.59]), the pooled negative likelihood ratio (NLR) was 0.36 (95% CI [0.31–0.43]), the pooled diagnostic odds ratio (DOR) was 10.00 (95% CI [7.73–12.95]), and the area under the curve 0.82 (95% CI [0.79–0.85]). A Deeks’ funnel plot shows that there was no publication bias (P = 0.99). CONCLUSION: Our findings suggest miR-21 might be the potential biomarker for detecting EC in Asian populations, with a good diagnostic value. PeerJ Inc. 2022-09-30 /pmc/articles/PMC9528905/ /pubmed/36199284 http://dx.doi.org/10.7717/peerj.14048 Text en © 2022 Han et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited. |
spellingShingle | Molecular Biology Han, Zheng Pan, Lingbo Lu, Bangjie Zhu, Huixia MicroRNA-21 as a potential biomarker for detecting esophageal carcinoma in Asian populations: a meta-analysis |
title | MicroRNA-21 as a potential biomarker for detecting esophageal carcinoma in Asian populations: a meta-analysis |
title_full | MicroRNA-21 as a potential biomarker for detecting esophageal carcinoma in Asian populations: a meta-analysis |
title_fullStr | MicroRNA-21 as a potential biomarker for detecting esophageal carcinoma in Asian populations: a meta-analysis |
title_full_unstemmed | MicroRNA-21 as a potential biomarker for detecting esophageal carcinoma in Asian populations: a meta-analysis |
title_short | MicroRNA-21 as a potential biomarker for detecting esophageal carcinoma in Asian populations: a meta-analysis |
title_sort | microrna-21 as a potential biomarker for detecting esophageal carcinoma in asian populations: a meta-analysis |
topic | Molecular Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9528905/ https://www.ncbi.nlm.nih.gov/pubmed/36199284 http://dx.doi.org/10.7717/peerj.14048 |
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