Circulating miRNA Expression Profiling and Target Prediction in Patients Receiving Dexmedetomidine

Background/Aims: Circulating miRNAs could serve as biomarkers for diagnosis or prognosis of heart diseases and cerebrovascular diseases. Dexmedetomidine has protective effects in various organs. The effects of dexmedetomidine on circulating miRNAs remain unknown. Here, we investigated differentially...

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Main Authors: Xuehui Yang, Hongmei Chen, Yan Chen, Yochai Birnbaum, Rongbi Liang, Yumei Ye, Jinqiao Qian
Format: Article
Language:English
Published: Cell Physiol Biochem Press GmbH & Co KG 2018-10-01
Series:Cellular Physiology and Biochemistry
Subjects:
Online Access:https://www.karger.com/Article/FullText/494168
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author Xuehui Yang
Hongmei Chen
Yan Chen
Yochai Birnbaum
Rongbi Liang
Yumei Ye
Jinqiao Qian
author_facet Xuehui Yang
Hongmei Chen
Yan Chen
Yochai Birnbaum
Rongbi Liang
Yumei Ye
Jinqiao Qian
author_sort Xuehui Yang
collection DOAJ
description Background/Aims: Circulating miRNAs could serve as biomarkers for diagnosis or prognosis of heart diseases and cerebrovascular diseases. Dexmedetomidine has protective effects in various organs. The effects of dexmedetomidine on circulating miRNAs remain unknown. Here, we investigated differentially expressed miRNA and to predict the target genes of the miRNA in patients receiving dexmedetomidine. Methods: The expression levels of circulating miRNAs of 3 patients were determined through high through-put miRNA sequencing technology. Target genes of the identified differentially expressed miRNAs were predicted using TargetScan 7.1 and miRDB v.5. Gene Ontology (GO) and the Kyoto Encyclopedia of Genes and Genomes (KEGG) were used to conduct functional annotation and pathway enrichment analysis of target genes respectively. Results: Twelve differentially expressed miRNAs were identified. Five miRNAs were upregulated (hsa-miR-4508, hsa-miR-novel-chr8_87373, hsa-miR-30a-3p, hsa-miR-novel-chr16_26099, hsa-miR-4306) and seven miRNAs (hsa-miR-744-5p, hsa-miR-320a, hsa-miR-novel-chr9_90035, hsa-miR-101-3p, hsa-miR-150-5p, hsa-miR-342-3p, and hsa-miR-140-3p) were downregulated after administration of dexmedetomidine in the subjects. The target genes and pathways related to the differentially expressed miRNAs were predicted and analyzed. Conclusion: The differentially expressed miRNAs may be involved in the mechanisms of action of dexmedetomidine. Specific miRNAs, such as hsa-miR-101-3p, hsa-miR-150-5p and hsa-miR-140-3p, are new potential targets for further functional studies of dexmedetomidine.
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spelling doaj.art-d0be67d94188414e937ed2c3af772d432022-12-22T02:37:06ZengCell Physiol Biochem Press GmbH & Co KGCellular Physiology and Biochemistry1015-89871421-97782018-10-0150255256810.1159/000494168494168Circulating miRNA Expression Profiling and Target Prediction in Patients Receiving DexmedetomidineXuehui YangHongmei ChenYan ChenYochai BirnbaumRongbi LiangYumei YeJinqiao QianBackground/Aims: Circulating miRNAs could serve as biomarkers for diagnosis or prognosis of heart diseases and cerebrovascular diseases. Dexmedetomidine has protective effects in various organs. The effects of dexmedetomidine on circulating miRNAs remain unknown. Here, we investigated differentially expressed miRNA and to predict the target genes of the miRNA in patients receiving dexmedetomidine. Methods: The expression levels of circulating miRNAs of 3 patients were determined through high through-put miRNA sequencing technology. Target genes of the identified differentially expressed miRNAs were predicted using TargetScan 7.1 and miRDB v.5. Gene Ontology (GO) and the Kyoto Encyclopedia of Genes and Genomes (KEGG) were used to conduct functional annotation and pathway enrichment analysis of target genes respectively. Results: Twelve differentially expressed miRNAs were identified. Five miRNAs were upregulated (hsa-miR-4508, hsa-miR-novel-chr8_87373, hsa-miR-30a-3p, hsa-miR-novel-chr16_26099, hsa-miR-4306) and seven miRNAs (hsa-miR-744-5p, hsa-miR-320a, hsa-miR-novel-chr9_90035, hsa-miR-101-3p, hsa-miR-150-5p, hsa-miR-342-3p, and hsa-miR-140-3p) were downregulated after administration of dexmedetomidine in the subjects. The target genes and pathways related to the differentially expressed miRNAs were predicted and analyzed. Conclusion: The differentially expressed miRNAs may be involved in the mechanisms of action of dexmedetomidine. Specific miRNAs, such as hsa-miR-101-3p, hsa-miR-150-5p and hsa-miR-140-3p, are new potential targets for further functional studies of dexmedetomidine.https://www.karger.com/Article/FullText/494168DexmedetomidineCirculating miRNAsExpression profilingIschemia/reperfusion injuryCardioprotection
spellingShingle Xuehui Yang
Hongmei Chen
Yan Chen
Yochai Birnbaum
Rongbi Liang
Yumei Ye
Jinqiao Qian
Circulating miRNA Expression Profiling and Target Prediction in Patients Receiving Dexmedetomidine
Cellular Physiology and Biochemistry
Dexmedetomidine
Circulating miRNAs
Expression profiling
Ischemia/reperfusion injury
Cardioprotection
title Circulating miRNA Expression Profiling and Target Prediction in Patients Receiving Dexmedetomidine
title_full Circulating miRNA Expression Profiling and Target Prediction in Patients Receiving Dexmedetomidine
title_fullStr Circulating miRNA Expression Profiling and Target Prediction in Patients Receiving Dexmedetomidine
title_full_unstemmed Circulating miRNA Expression Profiling and Target Prediction in Patients Receiving Dexmedetomidine
title_short Circulating miRNA Expression Profiling and Target Prediction in Patients Receiving Dexmedetomidine
title_sort circulating mirna expression profiling and target prediction in patients receiving dexmedetomidine
topic Dexmedetomidine
Circulating miRNAs
Expression profiling
Ischemia/reperfusion injury
Cardioprotection
url https://www.karger.com/Article/FullText/494168
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