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MicroRNA-21 and microRNA-30c as diagnostic biomarkers for prostate cancer: a meta-analysis
BACKGROUND: Prostate cancer (PCa) is the second leading cause of cancer death in men. Several articles have reported that microRNA-21 (miR-21) and microRNA-30c (miR-30c) have diagnostic values for PCa, but the results are inconclusive. In order to precisely assess the diagnostic values of miR-21 and...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6411321/ https://www.ncbi.nlm.nih.gov/pubmed/30881128 http://dx.doi.org/10.2147/CMAR.S189026 |
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author | Zhou, Hongxing Zhu, Xuming |
author_facet | Zhou, Hongxing Zhu, Xuming |
author_sort | Zhou, Hongxing |
collection | PubMed |
description | BACKGROUND: Prostate cancer (PCa) is the second leading cause of cancer death in men. Several articles have reported that microRNA-21 (miR-21) and microRNA-30c (miR-30c) have diagnostic values for PCa, but the results are inconclusive. In order to precisely assess the diagnostic values of miR-21 and miR-30c for PCa, this meta-analysis is performed. METHODS: Articles were searched in the databases of PubMed, Embase, and Web of Knowledge (search date: September 6, 2018). Studies were included if they were designed to evaluate the diagnostic performance of miR-21 or miR-30c for PCa. Using Stata 12.0 and Meta-Disc 1.4, the pooled sensitivity (SEN), specificity (SPE), positive likelihood ratio (PLR), negative likelihood ratio (NLR), diagnostic odds ratio (DOR), and area under curve (AUC) of the summary receiver-operating characteristic (SROC) curve with the corresponding 95% CI were calculated. RESULTS: Overall, ten studies (six studies for miR-21 and four for miR-30c) involving1,371 participants were included in this meta-analysis. For miR-21, the pooled SEN and SPE were, respectively, 0.91 (95% CI: 0.87–0.94) and 0.88 (95% CI: 0.82–0.93), the pooled PLR and NLR were, respectively, 7.74 (95% CI: 4.81–12.47), 0.1 (95% CI: 0.06–0.15), the DOR was 77.64 (95% CI: 34.64–174.02), AUC of SROC was 0.95 (95% CI: 0.93–0.97). For miR-30c, the pooled SEN and SPE were, respectively, 0.74 (95% CI: 0.65–0.81) and 0.78 (95% CI: 0.72–0.83), the pooled PLR and NLR were, respectively, 3.39 (95% CI: 2.69–4.26), and 0.34 (95% CI: 0.26–0.44), the DOR was 10.06 (95% CI: 6.96–14.55), and AUC of SROC was 0.83 (95% CI: 0.79–0.86). CONCLUSION: For PCa, miR-21 is a good diagnostic biomarker and miR-30c is a moderate diagnostic biomarker. |
format | Online Article Text |
id | pubmed-6411321 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-64113212019-03-16 MicroRNA-21 and microRNA-30c as diagnostic biomarkers for prostate cancer: a meta-analysis Zhou, Hongxing Zhu, Xuming Cancer Manag Res Original Research BACKGROUND: Prostate cancer (PCa) is the second leading cause of cancer death in men. Several articles have reported that microRNA-21 (miR-21) and microRNA-30c (miR-30c) have diagnostic values for PCa, but the results are inconclusive. In order to precisely assess the diagnostic values of miR-21 and miR-30c for PCa, this meta-analysis is performed. METHODS: Articles were searched in the databases of PubMed, Embase, and Web of Knowledge (search date: September 6, 2018). Studies were included if they were designed to evaluate the diagnostic performance of miR-21 or miR-30c for PCa. Using Stata 12.0 and Meta-Disc 1.4, the pooled sensitivity (SEN), specificity (SPE), positive likelihood ratio (PLR), negative likelihood ratio (NLR), diagnostic odds ratio (DOR), and area under curve (AUC) of the summary receiver-operating characteristic (SROC) curve with the corresponding 95% CI were calculated. RESULTS: Overall, ten studies (six studies for miR-21 and four for miR-30c) involving1,371 participants were included in this meta-analysis. For miR-21, the pooled SEN and SPE were, respectively, 0.91 (95% CI: 0.87–0.94) and 0.88 (95% CI: 0.82–0.93), the pooled PLR and NLR were, respectively, 7.74 (95% CI: 4.81–12.47), 0.1 (95% CI: 0.06–0.15), the DOR was 77.64 (95% CI: 34.64–174.02), AUC of SROC was 0.95 (95% CI: 0.93–0.97). For miR-30c, the pooled SEN and SPE were, respectively, 0.74 (95% CI: 0.65–0.81) and 0.78 (95% CI: 0.72–0.83), the pooled PLR and NLR were, respectively, 3.39 (95% CI: 2.69–4.26), and 0.34 (95% CI: 0.26–0.44), the DOR was 10.06 (95% CI: 6.96–14.55), and AUC of SROC was 0.83 (95% CI: 0.79–0.86). CONCLUSION: For PCa, miR-21 is a good diagnostic biomarker and miR-30c is a moderate diagnostic biomarker. Dove Medical Press 2019-03-06 /pmc/articles/PMC6411321/ /pubmed/30881128 http://dx.doi.org/10.2147/CMAR.S189026 Text en © 2019 Zhou and Zhu. 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. |
spellingShingle | Original Research Zhou, Hongxing Zhu, Xuming MicroRNA-21 and microRNA-30c as diagnostic biomarkers for prostate cancer: a meta-analysis |
title | MicroRNA-21 and microRNA-30c as diagnostic biomarkers for prostate cancer: a meta-analysis |
title_full | MicroRNA-21 and microRNA-30c as diagnostic biomarkers for prostate cancer: a meta-analysis |
title_fullStr | MicroRNA-21 and microRNA-30c as diagnostic biomarkers for prostate cancer: a meta-analysis |
title_full_unstemmed | MicroRNA-21 and microRNA-30c as diagnostic biomarkers for prostate cancer: a meta-analysis |
title_short | MicroRNA-21 and microRNA-30c as diagnostic biomarkers for prostate cancer: a meta-analysis |
title_sort | microrna-21 and microrna-30c as diagnostic biomarkers for prostate cancer: a meta-analysis |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6411321/ https://www.ncbi.nlm.nih.gov/pubmed/30881128 http://dx.doi.org/10.2147/CMAR.S189026 |
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