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Circulating microRNA expression and their target genes in deep vein thrombosis: A systematic review and bioinformatics analysis
BACKGROUND: Clinically, d-dimer is the only established biomarker for the diagnosis of deep vein thrombosis (DVT). However, low specificity discounts its diagnostic value. Several publications have illustrated the differentially expressed circulating microRNAs (miRNAs) and their potential diagnostic...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5815814/ https://www.ncbi.nlm.nih.gov/pubmed/29390402 http://dx.doi.org/10.1097/MD.0000000000009330 |
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author | Jiang, Zhiyun Ma, Junfen Wang, Qian Wu, Fan Ping, Jiedan Ming, Liang |
author_facet | Jiang, Zhiyun Ma, Junfen Wang, Qian Wu, Fan Ping, Jiedan Ming, Liang |
author_sort | Jiang, Zhiyun |
collection | PubMed |
description | BACKGROUND: Clinically, d-dimer is the only established biomarker for the diagnosis of deep vein thrombosis (DVT). However, low specificity discounts its diagnostic value. Several publications have illustrated the differentially expressed circulating microRNAs (miRNAs) and their potential diagnostic values for DVT patients. Therefore, we systematically evaluated present researches and further performed bioinformatics analysis, to provide new insights into the diagnosis and underlying mechanisms of miRNAs in DVT. METHODS: Databases PubMed, Web of Science, and Embase were searched from January 2000 to April 2017. Articles on circulating miRNAs expression in DVT were retrieved and reference lists were handpicked. Bioinformatics analysis was conducted for further evaluation. RESULTS: Eventually, the eligibility criteria for inclusion in this study were met by 3 articles, which consisted of 13 specially expressed miRNAs and 149 putative target genes. Two representative KEGG pathways, vascular endothelial growth factor and phosphatidylinositol 3’-kinase (PI3K)-Akt signaling pathway, seemed to participate in the regulatory network of thrombosis. CONCLUSIONS: Despite the potential diagnostic value and regulation effect, the results of circulating miRNAs used as biomarkers for DVT are not so encouraging. More in-depth and larger sample investigations are needed to explore the diagnostic and therapeutic values of miRNAs for DVT. |
format | Online Article Text |
id | pubmed-5815814 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-58158142018-02-28 Circulating microRNA expression and their target genes in deep vein thrombosis: A systematic review and bioinformatics analysis Jiang, Zhiyun Ma, Junfen Wang, Qian Wu, Fan Ping, Jiedan Ming, Liang Medicine (Baltimore) 4100 BACKGROUND: Clinically, d-dimer is the only established biomarker for the diagnosis of deep vein thrombosis (DVT). However, low specificity discounts its diagnostic value. Several publications have illustrated the differentially expressed circulating microRNAs (miRNAs) and their potential diagnostic values for DVT patients. Therefore, we systematically evaluated present researches and further performed bioinformatics analysis, to provide new insights into the diagnosis and underlying mechanisms of miRNAs in DVT. METHODS: Databases PubMed, Web of Science, and Embase were searched from January 2000 to April 2017. Articles on circulating miRNAs expression in DVT were retrieved and reference lists were handpicked. Bioinformatics analysis was conducted for further evaluation. RESULTS: Eventually, the eligibility criteria for inclusion in this study were met by 3 articles, which consisted of 13 specially expressed miRNAs and 149 putative target genes. Two representative KEGG pathways, vascular endothelial growth factor and phosphatidylinositol 3’-kinase (PI3K)-Akt signaling pathway, seemed to participate in the regulatory network of thrombosis. CONCLUSIONS: Despite the potential diagnostic value and regulation effect, the results of circulating miRNAs used as biomarkers for DVT are not so encouraging. More in-depth and larger sample investigations are needed to explore the diagnostic and therapeutic values of miRNAs for DVT. Wolters Kluwer Health 2017-12-15 /pmc/articles/PMC5815814/ /pubmed/29390402 http://dx.doi.org/10.1097/MD.0000000000009330 Text en Copyright © 2017 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by-nc/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial License 4.0 (CCBY-NC), where it is permissible to download, share, remix, transform, and buildup the work provided it is properly cited. The work cannot be used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc/4.0 |
spellingShingle | 4100 Jiang, Zhiyun Ma, Junfen Wang, Qian Wu, Fan Ping, Jiedan Ming, Liang Circulating microRNA expression and their target genes in deep vein thrombosis: A systematic review and bioinformatics analysis |
title | Circulating microRNA expression and their target genes in deep vein thrombosis: A systematic review and bioinformatics analysis |
title_full | Circulating microRNA expression and their target genes in deep vein thrombosis: A systematic review and bioinformatics analysis |
title_fullStr | Circulating microRNA expression and their target genes in deep vein thrombosis: A systematic review and bioinformatics analysis |
title_full_unstemmed | Circulating microRNA expression and their target genes in deep vein thrombosis: A systematic review and bioinformatics analysis |
title_short | Circulating microRNA expression and their target genes in deep vein thrombosis: A systematic review and bioinformatics analysis |
title_sort | circulating microrna expression and their target genes in deep vein thrombosis: a systematic review and bioinformatics analysis |
topic | 4100 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5815814/ https://www.ncbi.nlm.nih.gov/pubmed/29390402 http://dx.doi.org/10.1097/MD.0000000000009330 |
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