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Exosomal Long Non-Coding RNA Expression from Serum of Patients with Acute Minor Stroke

BACKGROUND: Acute minor stroke (AMS) is one kind of hypoxic ischemic necrosis with no more than 4 National Institutes of Health Stroke Scale (NIHSS) score. However, the early diagnosis of AMS is tough for lack of effective molecular markers. Recently, many long non-coding RNAs (lncRNAs) associated w...

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Autores principales: Xu, Xiaonan, Zhuang, Chengle, Chen, Liming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6968802/
https://www.ncbi.nlm.nih.gov/pubmed/32021207
http://dx.doi.org/10.2147/NDT.S230332
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author Xu, Xiaonan
Zhuang, Chengle
Chen, Liming
author_facet Xu, Xiaonan
Zhuang, Chengle
Chen, Liming
author_sort Xu, Xiaonan
collection PubMed
description BACKGROUND: Acute minor stroke (AMS) is one kind of hypoxic ischemic necrosis with no more than 4 National Institutes of Health Stroke Scale (NIHSS) score. However, the early diagnosis of AMS is tough for lack of effective molecular markers. Recently, many long non-coding RNAs (lncRNAs) associated with AMS have been gradually revealed. Here, we aim to find the potential biomarkers of lncRNAs in exosomes isolated from blood serum of patients with AMS for early detection. METHODS: RNA-seq technique, KEGG pathway analysis and GO enrichment analysis were used in this study. Besides, reverse transcription real-time quantitative polymerase chain reaction (RT-qPCR) was used to validate expression levels of four of eleven differentially expressed lncRNAs (lnc-CRKL-2, lnc-NTRK3-4, RPS6KA2-AS1 and lnc-CALM1-7) involved in the neurotrophin signaling pathway. RESULTS: The expression levels of lnc-CRKL-2 (mean value 48, standard deviation 4.583, P = 0.003) and lnc-NTRK3-4 (mean value 32.3, standard deviation 2.08, P = 0.001) were increased significantly in AMS patients, while the expression levels of RPS6KA2-AS1 (mean value −118.7, standard deviation 7.09, P = 0.001) and lnc-CALM1-7 (mean value −148.7, standard deviation 6.10, P = 0.001) were decreased dramatically. CONCLUSION: In conclusion, these four new revealed lncRNAs may be used as novel joint biomarkers for the early detection of AMS.
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spelling pubmed-69688022020-02-04 Exosomal Long Non-Coding RNA Expression from Serum of Patients with Acute Minor Stroke Xu, Xiaonan Zhuang, Chengle Chen, Liming Neuropsychiatr Dis Treat Original Research BACKGROUND: Acute minor stroke (AMS) is one kind of hypoxic ischemic necrosis with no more than 4 National Institutes of Health Stroke Scale (NIHSS) score. However, the early diagnosis of AMS is tough for lack of effective molecular markers. Recently, many long non-coding RNAs (lncRNAs) associated with AMS have been gradually revealed. Here, we aim to find the potential biomarkers of lncRNAs in exosomes isolated from blood serum of patients with AMS for early detection. METHODS: RNA-seq technique, KEGG pathway analysis and GO enrichment analysis were used in this study. Besides, reverse transcription real-time quantitative polymerase chain reaction (RT-qPCR) was used to validate expression levels of four of eleven differentially expressed lncRNAs (lnc-CRKL-2, lnc-NTRK3-4, RPS6KA2-AS1 and lnc-CALM1-7) involved in the neurotrophin signaling pathway. RESULTS: The expression levels of lnc-CRKL-2 (mean value 48, standard deviation 4.583, P = 0.003) and lnc-NTRK3-4 (mean value 32.3, standard deviation 2.08, P = 0.001) were increased significantly in AMS patients, while the expression levels of RPS6KA2-AS1 (mean value −118.7, standard deviation 7.09, P = 0.001) and lnc-CALM1-7 (mean value −148.7, standard deviation 6.10, P = 0.001) were decreased dramatically. CONCLUSION: In conclusion, these four new revealed lncRNAs may be used as novel joint biomarkers for the early detection of AMS. Dove 2020-01-13 /pmc/articles/PMC6968802/ /pubmed/32021207 http://dx.doi.org/10.2147/NDT.S230332 Text en © 2020 Xu et al. http://creativecommons.org/licenses/by-nc/3.0/ 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. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Xu, Xiaonan
Zhuang, Chengle
Chen, Liming
Exosomal Long Non-Coding RNA Expression from Serum of Patients with Acute Minor Stroke
title Exosomal Long Non-Coding RNA Expression from Serum of Patients with Acute Minor Stroke
title_full Exosomal Long Non-Coding RNA Expression from Serum of Patients with Acute Minor Stroke
title_fullStr Exosomal Long Non-Coding RNA Expression from Serum of Patients with Acute Minor Stroke
title_full_unstemmed Exosomal Long Non-Coding RNA Expression from Serum of Patients with Acute Minor Stroke
title_short Exosomal Long Non-Coding RNA Expression from Serum of Patients with Acute Minor Stroke
title_sort exosomal long non-coding rna expression from serum of patients with acute minor stroke
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6968802/
https://www.ncbi.nlm.nih.gov/pubmed/32021207
http://dx.doi.org/10.2147/NDT.S230332
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