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Identification of key genes associated with multiple sclerosis based on gene expression data from peripheral blood mononuclear cells
The aim of this study was to identify the potential key candidate genes of multiple sclerosis (MS) and uncover mechanisms in MS. We combined data from the microarray expression profile of three MS stages and performed bioinformatics analysis. Differentially expressed genes (DEGs) were identified amo...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
PeerJ Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7003695/ https://www.ncbi.nlm.nih.gov/pubmed/32117605 http://dx.doi.org/10.7717/peerj.8357 |
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author | Shang, Zhenwei Sun, Wenjing Zhang, Mingming Xu, Lidan Jia, Xueyuan Zhang, Ruijie Fu, Songbin |
author_facet | Shang, Zhenwei Sun, Wenjing Zhang, Mingming Xu, Lidan Jia, Xueyuan Zhang, Ruijie Fu, Songbin |
author_sort | Shang, Zhenwei |
collection | PubMed |
description | The aim of this study was to identify the potential key candidate genes of multiple sclerosis (MS) and uncover mechanisms in MS. We combined data from the microarray expression profile of three MS stages and performed bioinformatics analysis. Differentially expressed genes (DEGs) were identified among the distinct stages of MS and healthy controls, and a total of 349 shared DEGs were identified. Gene ontology (GO) and pathway enrichment analyses showed that the DEGs were significantly enriched in the biological processes (BPs) of purine-related metabolic processes and signaling, especially the common DEGs, which were enriched in some immunological processes. Most of the DEGs were enriched in signaling pathways associated with the immune system, some immune diseases and infectious disease pathways. Through a protein–protein interaction (PPI) network analysis and a gene expression regulatory network constructed with MS-related miRNAs, we confirmed FOS, TP53, VEGFA, JUN, HIF1A, RB1, PTGS2, CXCL8, OAS2, NFKBIA and OAS1 as candidate genes of MS. Furthermore , we explored the potential SNPs associated with MS by database mining. In conclusion, this study provides the identified genes, SNPs, biological processes, and cellular pathways associated with MS. The uncovered candidate genes may be potential biomarkers involved in the diagnosis and therapy of MS. |
format | Online Article Text |
id | pubmed-7003695 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | PeerJ Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-70036952020-02-28 Identification of key genes associated with multiple sclerosis based on gene expression data from peripheral blood mononuclear cells Shang, Zhenwei Sun, Wenjing Zhang, Mingming Xu, Lidan Jia, Xueyuan Zhang, Ruijie Fu, Songbin PeerJ Bioinformatics The aim of this study was to identify the potential key candidate genes of multiple sclerosis (MS) and uncover mechanisms in MS. We combined data from the microarray expression profile of three MS stages and performed bioinformatics analysis. Differentially expressed genes (DEGs) were identified among the distinct stages of MS and healthy controls, and a total of 349 shared DEGs were identified. Gene ontology (GO) and pathway enrichment analyses showed that the DEGs were significantly enriched in the biological processes (BPs) of purine-related metabolic processes and signaling, especially the common DEGs, which were enriched in some immunological processes. Most of the DEGs were enriched in signaling pathways associated with the immune system, some immune diseases and infectious disease pathways. Through a protein–protein interaction (PPI) network analysis and a gene expression regulatory network constructed with MS-related miRNAs, we confirmed FOS, TP53, VEGFA, JUN, HIF1A, RB1, PTGS2, CXCL8, OAS2, NFKBIA and OAS1 as candidate genes of MS. Furthermore , we explored the potential SNPs associated with MS by database mining. In conclusion, this study provides the identified genes, SNPs, biological processes, and cellular pathways associated with MS. The uncovered candidate genes may be potential biomarkers involved in the diagnosis and therapy of MS. PeerJ Inc. 2020-02-03 /pmc/articles/PMC7003695/ /pubmed/32117605 http://dx.doi.org/10.7717/peerj.8357 Text en ©2020 Shang et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited. |
spellingShingle | Bioinformatics Shang, Zhenwei Sun, Wenjing Zhang, Mingming Xu, Lidan Jia, Xueyuan Zhang, Ruijie Fu, Songbin Identification of key genes associated with multiple sclerosis based on gene expression data from peripheral blood mononuclear cells |
title | Identification of key genes associated with multiple sclerosis based on gene expression data from peripheral blood mononuclear cells |
title_full | Identification of key genes associated with multiple sclerosis based on gene expression data from peripheral blood mononuclear cells |
title_fullStr | Identification of key genes associated with multiple sclerosis based on gene expression data from peripheral blood mononuclear cells |
title_full_unstemmed | Identification of key genes associated with multiple sclerosis based on gene expression data from peripheral blood mononuclear cells |
title_short | Identification of key genes associated with multiple sclerosis based on gene expression data from peripheral blood mononuclear cells |
title_sort | identification of key genes associated with multiple sclerosis based on gene expression data from peripheral blood mononuclear cells |
topic | Bioinformatics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7003695/ https://www.ncbi.nlm.nih.gov/pubmed/32117605 http://dx.doi.org/10.7717/peerj.8357 |
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