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Changes in Whole-Blood microRNA Profiles during the Onset and Treatment Process of Cerebral Infarction: A Human Study

Circulating miRNA species are promising symptom markers for various diseases, including cardiovascular disease. However, studies regarding their role in the treatment process are limited, especially concerning cerebral infarction. This study aimed to extract miRNA markers to investigate whether they...

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Autores principales: Abe, Arata, Tanaka, Mayui, Yasuoka, Akihito, Saito, Yoshikazu, Okada, Shinji, Mishina, Masahiro, Abe, Keiko, Kimura, Kazumi, Asakura, Tomiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7246837/
https://www.ncbi.nlm.nih.gov/pubmed/32354168
http://dx.doi.org/10.3390/ijms21093107
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author Abe, Arata
Tanaka, Mayui
Yasuoka, Akihito
Saito, Yoshikazu
Okada, Shinji
Mishina, Masahiro
Abe, Keiko
Kimura, Kazumi
Asakura, Tomiko
author_facet Abe, Arata
Tanaka, Mayui
Yasuoka, Akihito
Saito, Yoshikazu
Okada, Shinji
Mishina, Masahiro
Abe, Keiko
Kimura, Kazumi
Asakura, Tomiko
author_sort Abe, Arata
collection PubMed
description Circulating miRNA species are promising symptom markers for various diseases, including cardiovascular disease. However, studies regarding their role in the treatment process are limited, especially concerning cerebral infarction. This study aimed to extract miRNA markers to investigate whether they reflect both onset and treatment process of cerebral infarction. A total of 22 patients (P-group) and 22 control subjects (C-group) were examined for their whole-blood miRNA profiles using DNA GeneChip™ miRNA 4.0 Array, with six patients examined after treatment (T-group). A total of 64 miRNAs were found to be differentially expressed between the C- and P-groups. Out of 64 miRNAs, the expression levels of two miRNAs correlated with hypertension. A total of 155 miRNAs were differentially expressed between the P- and T-groups. Five common miRNAs were found among the 64 and 155 miRNAs identified. Importantly, these common miRNAs were inversely regulated in each comparison (e.g., C < P > T), including miR-505-5p, which was previously reported to be upregulated in aortic stenosis patients. Our previous study using rat cerebral infarction models detected the downregulation of an apoptosis repressor, WDR26, which was repressed by one of the five miRNAs. Our results provide novel information regarding the miRNA-based diagnosis of cerebral infarction in humans. In particular, the five common miRNAs could be useful makers for the onset and the treatment process. Trial registration: This study was registered in the UMIN Clinical Trials Registry (UMIN000038321).
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spelling pubmed-72468372020-06-02 Changes in Whole-Blood microRNA Profiles during the Onset and Treatment Process of Cerebral Infarction: A Human Study Abe, Arata Tanaka, Mayui Yasuoka, Akihito Saito, Yoshikazu Okada, Shinji Mishina, Masahiro Abe, Keiko Kimura, Kazumi Asakura, Tomiko Int J Mol Sci Article Circulating miRNA species are promising symptom markers for various diseases, including cardiovascular disease. However, studies regarding their role in the treatment process are limited, especially concerning cerebral infarction. This study aimed to extract miRNA markers to investigate whether they reflect both onset and treatment process of cerebral infarction. A total of 22 patients (P-group) and 22 control subjects (C-group) were examined for their whole-blood miRNA profiles using DNA GeneChip™ miRNA 4.0 Array, with six patients examined after treatment (T-group). A total of 64 miRNAs were found to be differentially expressed between the C- and P-groups. Out of 64 miRNAs, the expression levels of two miRNAs correlated with hypertension. A total of 155 miRNAs were differentially expressed between the P- and T-groups. Five common miRNAs were found among the 64 and 155 miRNAs identified. Importantly, these common miRNAs were inversely regulated in each comparison (e.g., C < P > T), including miR-505-5p, which was previously reported to be upregulated in aortic stenosis patients. Our previous study using rat cerebral infarction models detected the downregulation of an apoptosis repressor, WDR26, which was repressed by one of the five miRNAs. Our results provide novel information regarding the miRNA-based diagnosis of cerebral infarction in humans. In particular, the five common miRNAs could be useful makers for the onset and the treatment process. Trial registration: This study was registered in the UMIN Clinical Trials Registry (UMIN000038321). MDPI 2020-04-28 /pmc/articles/PMC7246837/ /pubmed/32354168 http://dx.doi.org/10.3390/ijms21093107 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Abe, Arata
Tanaka, Mayui
Yasuoka, Akihito
Saito, Yoshikazu
Okada, Shinji
Mishina, Masahiro
Abe, Keiko
Kimura, Kazumi
Asakura, Tomiko
Changes in Whole-Blood microRNA Profiles during the Onset and Treatment Process of Cerebral Infarction: A Human Study
title Changes in Whole-Blood microRNA Profiles during the Onset and Treatment Process of Cerebral Infarction: A Human Study
title_full Changes in Whole-Blood microRNA Profiles during the Onset and Treatment Process of Cerebral Infarction: A Human Study
title_fullStr Changes in Whole-Blood microRNA Profiles during the Onset and Treatment Process of Cerebral Infarction: A Human Study
title_full_unstemmed Changes in Whole-Blood microRNA Profiles during the Onset and Treatment Process of Cerebral Infarction: A Human Study
title_short Changes in Whole-Blood microRNA Profiles during the Onset and Treatment Process of Cerebral Infarction: A Human Study
title_sort changes in whole-blood microrna profiles during the onset and treatment process of cerebral infarction: a human study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7246837/
https://www.ncbi.nlm.nih.gov/pubmed/32354168
http://dx.doi.org/10.3390/ijms21093107
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