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Deep Sequencing of Plasma Exosomal microRNA Level in Psoriasis Vulgaris Patients

Psoriasis is a chronic skin disease affecting 1% to 3% of the world population. Psoriasis vulgaris (PV) is the most common form of psoriasis. PV patients suffer from inflamed, pruritic and painful lesions for years (even a lifetime). However, conventional drugs for PV are costly. Considering the nee...

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Autores principales: Chen, Xiu-Min, Yao, Dan-Ni, Wang, Mao-Jie, Wu, Xiao-Dong, Deng, Jing-Wen, Deng, Hao, Huang, Run-Yue, Lu, Chuan-Jian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9160332/
https://www.ncbi.nlm.nih.gov/pubmed/35665333
http://dx.doi.org/10.3389/fmed.2022.895564
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author Chen, Xiu-Min
Yao, Dan-Ni
Wang, Mao-Jie
Wu, Xiao-Dong
Deng, Jing-Wen
Deng, Hao
Huang, Run-Yue
Lu, Chuan-Jian
author_facet Chen, Xiu-Min
Yao, Dan-Ni
Wang, Mao-Jie
Wu, Xiao-Dong
Deng, Jing-Wen
Deng, Hao
Huang, Run-Yue
Lu, Chuan-Jian
author_sort Chen, Xiu-Min
collection PubMed
description Psoriasis is a chronic skin disease affecting 1% to 3% of the world population. Psoriasis vulgaris (PV) is the most common form of psoriasis. PV patients suffer from inflamed, pruritic and painful lesions for years (even a lifetime). However, conventional drugs for PV are costly. Considering the need for long-term treatment of PV, it is urgent to discover novel biomarkers and therapeutic targets. Plasma exosomal miRNAs have been identified as the reliable biomarkers and therapy targets of human diseases. Here, we described the levels of plasma exosomal miRNAs in PV patients and analyzed the functional features of differently expressed miRNAs and their potential target genes for the first time. We identified 1,182 miRNAs including 336 novel miRNAs and 246 differently expressed miRNAs in plasma exosomes of healthy people and PV patients. Furthermore, the functional analysis found differently expressed miRNA-regulated target genes enriched for specific GO terms including primary metabolic process, cellular metabolic process, metabolic process, organic substance metabolic process, and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway containing cellular processes, human diseases, metabolic pathways, metabolism and organismal systems. In addition, we found that some predicted target genes of differentially expressed miRNAs, such as CREB1, RUNX2, EGFR, are both involved in inflammatory response and metabolism. In summary, our study identifies many candidate miRNAs involved in PV, which could provide potential biomarkers for diagnosis of PV and targets for clinical therapies against PV.
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spelling pubmed-91603322022-06-03 Deep Sequencing of Plasma Exosomal microRNA Level in Psoriasis Vulgaris Patients Chen, Xiu-Min Yao, Dan-Ni Wang, Mao-Jie Wu, Xiao-Dong Deng, Jing-Wen Deng, Hao Huang, Run-Yue Lu, Chuan-Jian Front Med (Lausanne) Medicine Psoriasis is a chronic skin disease affecting 1% to 3% of the world population. Psoriasis vulgaris (PV) is the most common form of psoriasis. PV patients suffer from inflamed, pruritic and painful lesions for years (even a lifetime). However, conventional drugs for PV are costly. Considering the need for long-term treatment of PV, it is urgent to discover novel biomarkers and therapeutic targets. Plasma exosomal miRNAs have been identified as the reliable biomarkers and therapy targets of human diseases. Here, we described the levels of plasma exosomal miRNAs in PV patients and analyzed the functional features of differently expressed miRNAs and their potential target genes for the first time. We identified 1,182 miRNAs including 336 novel miRNAs and 246 differently expressed miRNAs in plasma exosomes of healthy people and PV patients. Furthermore, the functional analysis found differently expressed miRNA-regulated target genes enriched for specific GO terms including primary metabolic process, cellular metabolic process, metabolic process, organic substance metabolic process, and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway containing cellular processes, human diseases, metabolic pathways, metabolism and organismal systems. In addition, we found that some predicted target genes of differentially expressed miRNAs, such as CREB1, RUNX2, EGFR, are both involved in inflammatory response and metabolism. In summary, our study identifies many candidate miRNAs involved in PV, which could provide potential biomarkers for diagnosis of PV and targets for clinical therapies against PV. Frontiers Media S.A. 2022-05-19 /pmc/articles/PMC9160332/ /pubmed/35665333 http://dx.doi.org/10.3389/fmed.2022.895564 Text en Copyright © 2022 Chen, Yao, Wang, Wu, Deng, Deng, Huang and Lu. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Medicine
Chen, Xiu-Min
Yao, Dan-Ni
Wang, Mao-Jie
Wu, Xiao-Dong
Deng, Jing-Wen
Deng, Hao
Huang, Run-Yue
Lu, Chuan-Jian
Deep Sequencing of Plasma Exosomal microRNA Level in Psoriasis Vulgaris Patients
title Deep Sequencing of Plasma Exosomal microRNA Level in Psoriasis Vulgaris Patients
title_full Deep Sequencing of Plasma Exosomal microRNA Level in Psoriasis Vulgaris Patients
title_fullStr Deep Sequencing of Plasma Exosomal microRNA Level in Psoriasis Vulgaris Patients
title_full_unstemmed Deep Sequencing of Plasma Exosomal microRNA Level in Psoriasis Vulgaris Patients
title_short Deep Sequencing of Plasma Exosomal microRNA Level in Psoriasis Vulgaris Patients
title_sort deep sequencing of plasma exosomal microrna level in psoriasis vulgaris patients
topic Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9160332/
https://www.ncbi.nlm.nih.gov/pubmed/35665333
http://dx.doi.org/10.3389/fmed.2022.895564
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