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Identification of Blood Let-7e-5p as a Biomarker for Ischemic Stroke

Circulating microRNAs (miRNAs) are emerging as novel disease biomarkers. Using a miRNA microarray, we previously showed that the whole blood level of let-7e-5p was significantly higher in ischemic stroke patients than in control subjects. However, the association between let-7e-5p expression and the...

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Autores principales: Huang, Suli, Lv, Ziquan, Guo, Yi, Li, Lu, Zhang, Yanwei, Zhou, Li, Yang, Binyao, Wu, Shuang, Zhang, Ying, Xie, Changhui, Li, Shanshan, Cheng, Jinquan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5077157/
https://www.ncbi.nlm.nih.gov/pubmed/27776139
http://dx.doi.org/10.1371/journal.pone.0163951
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author Huang, Suli
Lv, Ziquan
Guo, Yi
Li, Lu
Zhang, Yanwei
Zhou, Li
Yang, Binyao
Wu, Shuang
Zhang, Ying
Xie, Changhui
Li, Shanshan
Cheng, Jinquan
author_facet Huang, Suli
Lv, Ziquan
Guo, Yi
Li, Lu
Zhang, Yanwei
Zhou, Li
Yang, Binyao
Wu, Shuang
Zhang, Ying
Xie, Changhui
Li, Shanshan
Cheng, Jinquan
author_sort Huang, Suli
collection PubMed
description Circulating microRNAs (miRNAs) are emerging as novel disease biomarkers. Using a miRNA microarray, we previously showed that the whole blood level of let-7e-5p was significantly higher in ischemic stroke patients than in control subjects. However, the association between let-7e-5p expression and the occurrence of ischemic stroke remains unknown. In this study, we validated the expression levels of let-7e-5p in two case-control populations using miRNA TaqMan assays and further investigated the potential targets of let-7e-5p. The results suggest that the blood level of let-7e-5p was significantly higher in patients with ischemic stroke than in controls (p<0.05). Higher levels of let-7e-5p were associated with increased occurrence of ischemic stroke (adjusted OR, 1.89; 95% CI, 1.61~2.21, p<0.001) in the combined population. The addition of let-7e-5p to traditional risk factors led to an improvement in the area under the curve, which increased from 0.74 (95% CI, 0.70~0.78) to 0.82 (95% CI, 0.78~0.85), with a net reclassification improvement of 16.76% (p<0.0001) and an integrated discrimination improvement of 0.10 (p<0.0001) for patients with ischemic stroke. Bioinformatics prediction and cell experiments suggested that the expression levels of four genes enriched in the MAPK signaling pathway were down-regulated by let-7e-5p transfection. Specifically, the expression levels of the genes CASP3 and NLK were significantly lower in ischemic stroke patients than in controls and were negatively correlated with let-7e-5p expression. In summary, our study suggests the potential use of blood let-7e-5p as a biomarker for ischemic stroke and indicates its involvement in the related pathomechanism.
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spelling pubmed-50771572016-11-04 Identification of Blood Let-7e-5p as a Biomarker for Ischemic Stroke Huang, Suli Lv, Ziquan Guo, Yi Li, Lu Zhang, Yanwei Zhou, Li Yang, Binyao Wu, Shuang Zhang, Ying Xie, Changhui Li, Shanshan Cheng, Jinquan PLoS One Research Article Circulating microRNAs (miRNAs) are emerging as novel disease biomarkers. Using a miRNA microarray, we previously showed that the whole blood level of let-7e-5p was significantly higher in ischemic stroke patients than in control subjects. However, the association between let-7e-5p expression and the occurrence of ischemic stroke remains unknown. In this study, we validated the expression levels of let-7e-5p in two case-control populations using miRNA TaqMan assays and further investigated the potential targets of let-7e-5p. The results suggest that the blood level of let-7e-5p was significantly higher in patients with ischemic stroke than in controls (p<0.05). Higher levels of let-7e-5p were associated with increased occurrence of ischemic stroke (adjusted OR, 1.89; 95% CI, 1.61~2.21, p<0.001) in the combined population. The addition of let-7e-5p to traditional risk factors led to an improvement in the area under the curve, which increased from 0.74 (95% CI, 0.70~0.78) to 0.82 (95% CI, 0.78~0.85), with a net reclassification improvement of 16.76% (p<0.0001) and an integrated discrimination improvement of 0.10 (p<0.0001) for patients with ischemic stroke. Bioinformatics prediction and cell experiments suggested that the expression levels of four genes enriched in the MAPK signaling pathway were down-regulated by let-7e-5p transfection. Specifically, the expression levels of the genes CASP3 and NLK were significantly lower in ischemic stroke patients than in controls and were negatively correlated with let-7e-5p expression. In summary, our study suggests the potential use of blood let-7e-5p as a biomarker for ischemic stroke and indicates its involvement in the related pathomechanism. Public Library of Science 2016-10-24 /pmc/articles/PMC5077157/ /pubmed/27776139 http://dx.doi.org/10.1371/journal.pone.0163951 Text en © 2016 Huang et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Huang, Suli
Lv, Ziquan
Guo, Yi
Li, Lu
Zhang, Yanwei
Zhou, Li
Yang, Binyao
Wu, Shuang
Zhang, Ying
Xie, Changhui
Li, Shanshan
Cheng, Jinquan
Identification of Blood Let-7e-5p as a Biomarker for Ischemic Stroke
title Identification of Blood Let-7e-5p as a Biomarker for Ischemic Stroke
title_full Identification of Blood Let-7e-5p as a Biomarker for Ischemic Stroke
title_fullStr Identification of Blood Let-7e-5p as a Biomarker for Ischemic Stroke
title_full_unstemmed Identification of Blood Let-7e-5p as a Biomarker for Ischemic Stroke
title_short Identification of Blood Let-7e-5p as a Biomarker for Ischemic Stroke
title_sort identification of blood let-7e-5p as a biomarker for ischemic stroke
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5077157/
https://www.ncbi.nlm.nih.gov/pubmed/27776139
http://dx.doi.org/10.1371/journal.pone.0163951
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