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MicroRNAs as a novel class of diagnostic biomarkers for the detection of osteosarcoma: a meta-analysis

MicroRNAs (miRNAs) have been considered as promising diagnostic biomarkers for many diseases, especially for cancers. Numerous studies have reported the value of miRNAs in the diagnosis of osteosarcoma (OS), but the results vary greatly across different studies. Therefore, we conducted this meta-ana...

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Autores principales: Liu, Hong, Li, Ping, Chen, Liang, Jian, Chao, Li, Zonghuan, Yu, Aixi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5677380/
https://www.ncbi.nlm.nih.gov/pubmed/29138575
http://dx.doi.org/10.2147/OTT.S143974
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author Liu, Hong
Li, Ping
Chen, Liang
Jian, Chao
Li, Zonghuan
Yu, Aixi
author_facet Liu, Hong
Li, Ping
Chen, Liang
Jian, Chao
Li, Zonghuan
Yu, Aixi
author_sort Liu, Hong
collection PubMed
description MicroRNAs (miRNAs) have been considered as promising diagnostic biomarkers for many diseases, especially for cancers. Numerous studies have reported the value of miRNAs in the diagnosis of osteosarcoma (OS), but the results vary greatly across different studies. Therefore, we conducted this meta-analysis to assess the prospective diagnostic value of miRNAs in diagnosing OS. All relevant articles from prior to July 28, 2017 were selected from PubMed, EMBASE, Web of Science, Cochrane Library, Chinese National Knowledge Infrastructure, and Wan-fang databases. The Quality Assessment of Diagnostic Accuracy Studies-2 (QUADAS-2) was performed to assess the quality of each article. A random-effects model was used to pool the sensitivity and specificity of the positive likelihood ratio (PLR), negative likelihood ratio (NLR) and, diagnostic odds ratio (DOR) together with the area under the curve (AUC) to evaluate diagnostic values. Seventeen studies comprising 2,214 OS patients and 1,534 healthy humans were included in our meta-analysis. The pooled estimations indicated that the miRNAs had a high accuracy for diagnosing OS, with a sensitivity of 0.82, specificity of 0.88, PLR of 10.96, NLR of 0.20, DOR of 54.55, and AUC of 0.93. Twenty-five miRNAs were differentially expressed in OS, including 17 upregulated and 8 downregulated. These miRNAs were correlated with survival time, tumor size, cell differentiation, tumor node metastasis staging, metastasis, tumor/cell invasion, pathological type, and response to radiotherapy and chemotherapy. Several different miRNAs are expressed in OS, and some of them might be potential biomarkers for the early diagnosis of OS.
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spelling pubmed-56773802017-11-14 MicroRNAs as a novel class of diagnostic biomarkers for the detection of osteosarcoma: a meta-analysis Liu, Hong Li, Ping Chen, Liang Jian, Chao Li, Zonghuan Yu, Aixi Onco Targets Ther Original Research MicroRNAs (miRNAs) have been considered as promising diagnostic biomarkers for many diseases, especially for cancers. Numerous studies have reported the value of miRNAs in the diagnosis of osteosarcoma (OS), but the results vary greatly across different studies. Therefore, we conducted this meta-analysis to assess the prospective diagnostic value of miRNAs in diagnosing OS. All relevant articles from prior to July 28, 2017 were selected from PubMed, EMBASE, Web of Science, Cochrane Library, Chinese National Knowledge Infrastructure, and Wan-fang databases. The Quality Assessment of Diagnostic Accuracy Studies-2 (QUADAS-2) was performed to assess the quality of each article. A random-effects model was used to pool the sensitivity and specificity of the positive likelihood ratio (PLR), negative likelihood ratio (NLR) and, diagnostic odds ratio (DOR) together with the area under the curve (AUC) to evaluate diagnostic values. Seventeen studies comprising 2,214 OS patients and 1,534 healthy humans were included in our meta-analysis. The pooled estimations indicated that the miRNAs had a high accuracy for diagnosing OS, with a sensitivity of 0.82, specificity of 0.88, PLR of 10.96, NLR of 0.20, DOR of 54.55, and AUC of 0.93. Twenty-five miRNAs were differentially expressed in OS, including 17 upregulated and 8 downregulated. These miRNAs were correlated with survival time, tumor size, cell differentiation, tumor node metastasis staging, metastasis, tumor/cell invasion, pathological type, and response to radiotherapy and chemotherapy. Several different miRNAs are expressed in OS, and some of them might be potential biomarkers for the early diagnosis of OS. Dove Medical Press 2017-11-01 /pmc/articles/PMC5677380/ /pubmed/29138575 http://dx.doi.org/10.2147/OTT.S143974 Text en © 2017 Liu et al. 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
Liu, Hong
Li, Ping
Chen, Liang
Jian, Chao
Li, Zonghuan
Yu, Aixi
MicroRNAs as a novel class of diagnostic biomarkers for the detection of osteosarcoma: a meta-analysis
title MicroRNAs as a novel class of diagnostic biomarkers for the detection of osteosarcoma: a meta-analysis
title_full MicroRNAs as a novel class of diagnostic biomarkers for the detection of osteosarcoma: a meta-analysis
title_fullStr MicroRNAs as a novel class of diagnostic biomarkers for the detection of osteosarcoma: a meta-analysis
title_full_unstemmed MicroRNAs as a novel class of diagnostic biomarkers for the detection of osteosarcoma: a meta-analysis
title_short MicroRNAs as a novel class of diagnostic biomarkers for the detection of osteosarcoma: a meta-analysis
title_sort micrornas as a novel class of diagnostic biomarkers for the detection of osteosarcoma: a meta-analysis
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5677380/
https://www.ncbi.nlm.nih.gov/pubmed/29138575
http://dx.doi.org/10.2147/OTT.S143974
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