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Characteristics of circular RNA expression in lung tissues from mice with hypoxia-induced pulmonary hypertension

Pulmonary hypertension (PH) is a life-threatening lung disease, characterized by an increase in pulmonary arterial pressure caused by vasoconstriction and vascular remodeling. The pathogenesis of PH is not fully understood, and there is a lack of potential biomarkers for the diagnosis and treatment...

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Autores principales: Wang, Jian, Zhu, Meng-Chan, Kalionis, Bill, Wu, Jun-Zhen, Wang, Lin-Lin, Ge, Hai-Yan, Chen, Cui-Cui, Tang, Xiao-Dan, Song, Yuan-Lin, He, Hong, Xia, Shi-Jin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6089758/
https://www.ncbi.nlm.nih.gov/pubmed/29956720
http://dx.doi.org/10.3892/ijmm.2018.3740
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author Wang, Jian
Zhu, Meng-Chan
Kalionis, Bill
Wu, Jun-Zhen
Wang, Lin-Lin
Ge, Hai-Yan
Chen, Cui-Cui
Tang, Xiao-Dan
Song, Yuan-Lin
He, Hong
Xia, Shi-Jin
author_facet Wang, Jian
Zhu, Meng-Chan
Kalionis, Bill
Wu, Jun-Zhen
Wang, Lin-Lin
Ge, Hai-Yan
Chen, Cui-Cui
Tang, Xiao-Dan
Song, Yuan-Lin
He, Hong
Xia, Shi-Jin
author_sort Wang, Jian
collection PubMed
description Pulmonary hypertension (PH) is a life-threatening lung disease, characterized by an increase in pulmonary arterial pressure caused by vasoconstriction and vascular remodeling. The pathogenesis of PH is not fully understood, and there is a lack of potential biomarkers for the diagnosis and treatment of patients with PH. Non-coding RNAs with a characteristic covalently closed loop structure, termed circular RNAs (circRNAs), are present in a number of pulmonary diseases. To the best of our knowledge, the present study is the first to use microarray analysis to determine the expression profile of circRNAs in lung tissues from mice with hypoxia-induced PH. In total, 23 significantly upregulated and 41 significantly down-regulated circRNAs were identified. Of these, 12 differentially expressed circRNAs were selected for further validation using reverse transcription-quantitative polymerase chain reaction. Putative microRNAs (miRNAs) that bind to the dysregulated circRNAs were predicted. Subsequently, bioinformatics tools were used to construct circRNA-miRNA-mRNA networks for the two most promising circRNAs, namely mmu_circRNA_004592 and mmu_circRNA_018351. Gene Ontology and Kyoto Encyclopedia of Genes and Genomes analyses of target genes of the dysregulated circRNAs revealed that these dysregulated circRNAs may serve an important role in the pathogenesis of hypoxia-induced PH. Therefore, these dysregulated circRNAs are candidate diagnostic biomarkers and potential therapeutic targets for PH.
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spelling pubmed-60897582018-08-16 Characteristics of circular RNA expression in lung tissues from mice with hypoxia-induced pulmonary hypertension Wang, Jian Zhu, Meng-Chan Kalionis, Bill Wu, Jun-Zhen Wang, Lin-Lin Ge, Hai-Yan Chen, Cui-Cui Tang, Xiao-Dan Song, Yuan-Lin He, Hong Xia, Shi-Jin Int J Mol Med Articles Pulmonary hypertension (PH) is a life-threatening lung disease, characterized by an increase in pulmonary arterial pressure caused by vasoconstriction and vascular remodeling. The pathogenesis of PH is not fully understood, and there is a lack of potential biomarkers for the diagnosis and treatment of patients with PH. Non-coding RNAs with a characteristic covalently closed loop structure, termed circular RNAs (circRNAs), are present in a number of pulmonary diseases. To the best of our knowledge, the present study is the first to use microarray analysis to determine the expression profile of circRNAs in lung tissues from mice with hypoxia-induced PH. In total, 23 significantly upregulated and 41 significantly down-regulated circRNAs were identified. Of these, 12 differentially expressed circRNAs were selected for further validation using reverse transcription-quantitative polymerase chain reaction. Putative microRNAs (miRNAs) that bind to the dysregulated circRNAs were predicted. Subsequently, bioinformatics tools were used to construct circRNA-miRNA-mRNA networks for the two most promising circRNAs, namely mmu_circRNA_004592 and mmu_circRNA_018351. Gene Ontology and Kyoto Encyclopedia of Genes and Genomes analyses of target genes of the dysregulated circRNAs revealed that these dysregulated circRNAs may serve an important role in the pathogenesis of hypoxia-induced PH. Therefore, these dysregulated circRNAs are candidate diagnostic biomarkers and potential therapeutic targets for PH. D.A. Spandidos 2018-09 2018-06-21 /pmc/articles/PMC6089758/ /pubmed/29956720 http://dx.doi.org/10.3892/ijmm.2018.3740 Text en Copyright: © Wang et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
Wang, Jian
Zhu, Meng-Chan
Kalionis, Bill
Wu, Jun-Zhen
Wang, Lin-Lin
Ge, Hai-Yan
Chen, Cui-Cui
Tang, Xiao-Dan
Song, Yuan-Lin
He, Hong
Xia, Shi-Jin
Characteristics of circular RNA expression in lung tissues from mice with hypoxia-induced pulmonary hypertension
title Characteristics of circular RNA expression in lung tissues from mice with hypoxia-induced pulmonary hypertension
title_full Characteristics of circular RNA expression in lung tissues from mice with hypoxia-induced pulmonary hypertension
title_fullStr Characteristics of circular RNA expression in lung tissues from mice with hypoxia-induced pulmonary hypertension
title_full_unstemmed Characteristics of circular RNA expression in lung tissues from mice with hypoxia-induced pulmonary hypertension
title_short Characteristics of circular RNA expression in lung tissues from mice with hypoxia-induced pulmonary hypertension
title_sort characteristics of circular rna expression in lung tissues from mice with hypoxia-induced pulmonary hypertension
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6089758/
https://www.ncbi.nlm.nih.gov/pubmed/29956720
http://dx.doi.org/10.3892/ijmm.2018.3740
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