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The diagnostic role of microRNA-34a in breast cancer: a systematic review and meta-analysis
BACKGROUND: MicroRNA-34a (miR-34a) is a master regulator of tumor suppression in breast cancer (BC). This systematic review aims to analyze the diagnostic accuracy of miR-34a in the detection of BC as a biomarker. RESULTS: A total of 1858 BC cases and 494 controls from thirteen eligible studies repo...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5410295/ https://www.ncbi.nlm.nih.gov/pubmed/28423566 http://dx.doi.org/10.18632/oncotarget.15520 |
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author | Imani, Saber Zhang, Xianqin Hosseinifard, Hossein Fu, Shangyi Fu, Junjiang |
author_facet | Imani, Saber Zhang, Xianqin Hosseinifard, Hossein Fu, Shangyi Fu, Junjiang |
author_sort | Imani, Saber |
collection | PubMed |
description | BACKGROUND: MicroRNA-34a (miR-34a) is a master regulator of tumor suppression in breast cancer (BC). This systematic review aims to analyze the diagnostic accuracy of miR-34a in the detection of BC as a biomarker. RESULTS: A total of 1858 BC cases and 494 controls from thirteen eligible studies reported in 9 publications were included. The overall pooled sensitivity, specificity, negative likelihood ratio (NLR), positive likelihood ratio (PLR), and diagnostic odds ratio (DOR) were 85.50% (95% CI: 83.80-87.00%), 70.00% (95% CI: 65.80–74.10%), 0.29 (95% CI: 0.19–0.43), 2.58 (95% CI: 1.91–3.43), and 9.39 (95% CI: 5.47–16.12), respectively. Similarly, the overall area under the curve (AUC) of the summary receiver operating characteristic (SROC) was 0.80, indicating the high conservation of miR-34a as a biomarker. Furthermore, subgroup analysis suggested that the use of miR-34a as a biomarker is more accurate in tissue-based sample of invasive BC. We also indicated that miR-34a is a capable biomarker in diagnosing BC in people of Caucasian descent. MATERIALS AND METHODS: A systematic search was conducted for eligible publications that address miR-34a expression level in BC cases and noncancerous controls. Diagnostic capacity of miR-34a for BC was assessed using pooled sensitivity and specificity, DOR, and AUC of SROC. PLR and NLR were verified to estimate the miR-34a diagnostic accuracy in clinical level. The quality of the included studies was assessed by QUADAS-2. CONCLUSIONS: These findings suggest miR-34a is a promising non-invasive biomarker in diagnosing BC. Well-designed cohort studies should be implemented to warrant the diagnostic value of miR-34a in clinical purposes. |
format | Online Article Text |
id | pubmed-5410295 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-54102952017-05-04 The diagnostic role of microRNA-34a in breast cancer: a systematic review and meta-analysis Imani, Saber Zhang, Xianqin Hosseinifard, Hossein Fu, Shangyi Fu, Junjiang Oncotarget Research Paper BACKGROUND: MicroRNA-34a (miR-34a) is a master regulator of tumor suppression in breast cancer (BC). This systematic review aims to analyze the diagnostic accuracy of miR-34a in the detection of BC as a biomarker. RESULTS: A total of 1858 BC cases and 494 controls from thirteen eligible studies reported in 9 publications were included. The overall pooled sensitivity, specificity, negative likelihood ratio (NLR), positive likelihood ratio (PLR), and diagnostic odds ratio (DOR) were 85.50% (95% CI: 83.80-87.00%), 70.00% (95% CI: 65.80–74.10%), 0.29 (95% CI: 0.19–0.43), 2.58 (95% CI: 1.91–3.43), and 9.39 (95% CI: 5.47–16.12), respectively. Similarly, the overall area under the curve (AUC) of the summary receiver operating characteristic (SROC) was 0.80, indicating the high conservation of miR-34a as a biomarker. Furthermore, subgroup analysis suggested that the use of miR-34a as a biomarker is more accurate in tissue-based sample of invasive BC. We also indicated that miR-34a is a capable biomarker in diagnosing BC in people of Caucasian descent. MATERIALS AND METHODS: A systematic search was conducted for eligible publications that address miR-34a expression level in BC cases and noncancerous controls. Diagnostic capacity of miR-34a for BC was assessed using pooled sensitivity and specificity, DOR, and AUC of SROC. PLR and NLR were verified to estimate the miR-34a diagnostic accuracy in clinical level. The quality of the included studies was assessed by QUADAS-2. CONCLUSIONS: These findings suggest miR-34a is a promising non-invasive biomarker in diagnosing BC. Well-designed cohort studies should be implemented to warrant the diagnostic value of miR-34a in clinical purposes. Impact Journals LLC 2017-02-20 /pmc/articles/PMC5410295/ /pubmed/28423566 http://dx.doi.org/10.18632/oncotarget.15520 Text en Copyright: © 2017 Imani et al. http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) (CC-BY), which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Research Paper Imani, Saber Zhang, Xianqin Hosseinifard, Hossein Fu, Shangyi Fu, Junjiang The diagnostic role of microRNA-34a in breast cancer: a systematic review and meta-analysis |
title | The diagnostic role of microRNA-34a in breast cancer: a systematic review and meta-analysis |
title_full | The diagnostic role of microRNA-34a in breast cancer: a systematic review and meta-analysis |
title_fullStr | The diagnostic role of microRNA-34a in breast cancer: a systematic review and meta-analysis |
title_full_unstemmed | The diagnostic role of microRNA-34a in breast cancer: a systematic review and meta-analysis |
title_short | The diagnostic role of microRNA-34a in breast cancer: a systematic review and meta-analysis |
title_sort | diagnostic role of microrna-34a in breast cancer: a systematic review and meta-analysis |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5410295/ https://www.ncbi.nlm.nih.gov/pubmed/28423566 http://dx.doi.org/10.18632/oncotarget.15520 |
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