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Circulating microRNAs are promising novel biomarkers for drug-resistant epilepsy
MicroRNAs (miRNAs) open up a new field for molecular diagnosis for cancer and other diseases based on their stability in serum. However, the role of circulating miRNAs in plasma/serum in epilepsy diagnosis is still unclear. The aim of this study was to evaluate whether miRNAs can be used as biomarke...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4435024/ https://www.ncbi.nlm.nih.gov/pubmed/25984652 http://dx.doi.org/10.1038/srep10201 |
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author | Wang, Jun Tan, Lan Tan, Lin Tian, Yan Ma, Jing Tan, Chen-Chen Wang, Hui-Fu Liu, Ying Tan, Meng-Shan Jiang, Teng Yu, Jin-Tai |
author_facet | Wang, Jun Tan, Lan Tan, Lin Tian, Yan Ma, Jing Tan, Chen-Chen Wang, Hui-Fu Liu, Ying Tan, Meng-Shan Jiang, Teng Yu, Jin-Tai |
author_sort | Wang, Jun |
collection | PubMed |
description | MicroRNAs (miRNAs) open up a new field for molecular diagnosis for cancer and other diseases based on their stability in serum. However, the role of circulating miRNAs in plasma/serum in epilepsy diagnosis is still unclear. The aim of this study was to evaluate whether miRNAs can be used as biomarkers for drug-resistant epilepsy. We measured the differences in serum miRNA levels between 30 drug-resistant patients and 30 drug-responsive epilepsy patients in discovery and training phases using Illumina HiSeq2000 sequencing followed by quantitative reverse transcriptase polymerase chain reaction (qRT-PCR) assays. The selected miRNAs were then validated in 77 drug-resistant epilepsy patients, 81 drug-responsive epilepsy patients and 85 healthy controls by qRT-PCR. We found that circulating miRNAs are differentially expressed between drug-resistant group and drug-responsive group. MiR-194-5p, -301a-3p, -30b-5p, -342-5p and -4446-3p were significantly deregulated in drug-resistant group compared to drug-responsive group and control group. Among these 5 miRNAs, miR-301a-3p had the best diagnostic value for drug-resistant epilepsy with 80.5% sensitivity and 81.2% specificity, and was negatively associated with seizure severity. These provide the rationale for further confirmation studies in larger prospective cohorts and in other ethnics. |
format | Online Article Text |
id | pubmed-4435024 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-44350242015-05-28 Circulating microRNAs are promising novel biomarkers for drug-resistant epilepsy Wang, Jun Tan, Lan Tan, Lin Tian, Yan Ma, Jing Tan, Chen-Chen Wang, Hui-Fu Liu, Ying Tan, Meng-Shan Jiang, Teng Yu, Jin-Tai Sci Rep Article MicroRNAs (miRNAs) open up a new field for molecular diagnosis for cancer and other diseases based on their stability in serum. However, the role of circulating miRNAs in plasma/serum in epilepsy diagnosis is still unclear. The aim of this study was to evaluate whether miRNAs can be used as biomarkers for drug-resistant epilepsy. We measured the differences in serum miRNA levels between 30 drug-resistant patients and 30 drug-responsive epilepsy patients in discovery and training phases using Illumina HiSeq2000 sequencing followed by quantitative reverse transcriptase polymerase chain reaction (qRT-PCR) assays. The selected miRNAs were then validated in 77 drug-resistant epilepsy patients, 81 drug-responsive epilepsy patients and 85 healthy controls by qRT-PCR. We found that circulating miRNAs are differentially expressed between drug-resistant group and drug-responsive group. MiR-194-5p, -301a-3p, -30b-5p, -342-5p and -4446-3p were significantly deregulated in drug-resistant group compared to drug-responsive group and control group. Among these 5 miRNAs, miR-301a-3p had the best diagnostic value for drug-resistant epilepsy with 80.5% sensitivity and 81.2% specificity, and was negatively associated with seizure severity. These provide the rationale for further confirmation studies in larger prospective cohorts and in other ethnics. Nature Publishing Group 2015-05-18 /pmc/articles/PMC4435024/ /pubmed/25984652 http://dx.doi.org/10.1038/srep10201 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Wang, Jun Tan, Lan Tan, Lin Tian, Yan Ma, Jing Tan, Chen-Chen Wang, Hui-Fu Liu, Ying Tan, Meng-Shan Jiang, Teng Yu, Jin-Tai Circulating microRNAs are promising novel biomarkers for drug-resistant epilepsy |
title | Circulating microRNAs are promising novel biomarkers for drug-resistant epilepsy |
title_full | Circulating microRNAs are promising novel biomarkers for drug-resistant epilepsy |
title_fullStr | Circulating microRNAs are promising novel biomarkers for drug-resistant epilepsy |
title_full_unstemmed | Circulating microRNAs are promising novel biomarkers for drug-resistant epilepsy |
title_short | Circulating microRNAs are promising novel biomarkers for drug-resistant epilepsy |
title_sort | circulating micrornas are promising novel biomarkers for drug-resistant epilepsy |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4435024/ https://www.ncbi.nlm.nih.gov/pubmed/25984652 http://dx.doi.org/10.1038/srep10201 |
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