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Identification of Susceptibility Genes to Allergic Rhinitis by Gene Expression Data Sets
As an extremely prevalent disease worldwide, allergic rhinitis (AR) is a condition characterized by chronic inflammation of the nasal mucosa. To identify the finer molecular mechanisms associated with the AR susceptibility genes, differentially expressed genes (DEGs) in AR were investigated. The DEG...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6951973/ https://www.ncbi.nlm.nih.gov/pubmed/31794148 http://dx.doi.org/10.1111/cts.12698 |
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author | Xue, Kai Yang, Jingpu Zhao, Yin Cheng, Jinzhang Wang, Zonggui |
author_facet | Xue, Kai Yang, Jingpu Zhao, Yin Cheng, Jinzhang Wang, Zonggui |
author_sort | Xue, Kai |
collection | PubMed |
description | As an extremely prevalent disease worldwide, allergic rhinitis (AR) is a condition characterized by chronic inflammation of the nasal mucosa. To identify the finer molecular mechanisms associated with the AR susceptibility genes, differentially expressed genes (DEGs) in AR were investigated. The DEG expression and clinical data of the GSE19187 data set were used for weighted gene co‐expression network analysis (WGCNA). After the modules related to AR had been screened, the genes in the module were extracted for Gene Ontology and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment analysis, whereby the genes enriched in the KEGG pathway were regarded as the pathway‐genes. The DEGs in patients with AR were subsequently screened out from GSE19187, and the sensitive genes were identified in GSE18574 in connection with the allergen challenge. Two kinds of genes were compared with the pathway‐genes in order to screen the AR susceptibility genes. Receiver operating characteristic (ROC) curve was plotted to evaluate the capability of the susceptibility genes to distinguish the AR state. Based on the WGCNA in the GSE19187 data set, 10 co‐expression network modules were identified. The correlation analyses revealed that the yellow module was positively correlated with the disease state of AR. A total of 89 genes were found to be involved in the enrichment of the yellow module pathway. Four genes (CST1,SH2D1B,DPP4, and SLC5A5) were upregulated in AR and sensitive to allergen challenge, whose potentials were further confirmed by ROC curve. Taken together, CST1,SH2D1B,DPP4, and SLC5A5 are susceptibility genes to AR. |
format | Online Article Text |
id | pubmed-6951973 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-69519732020-01-10 Identification of Susceptibility Genes to Allergic Rhinitis by Gene Expression Data Sets Xue, Kai Yang, Jingpu Zhao, Yin Cheng, Jinzhang Wang, Zonggui Clin Transl Sci Research As an extremely prevalent disease worldwide, allergic rhinitis (AR) is a condition characterized by chronic inflammation of the nasal mucosa. To identify the finer molecular mechanisms associated with the AR susceptibility genes, differentially expressed genes (DEGs) in AR were investigated. The DEG expression and clinical data of the GSE19187 data set were used for weighted gene co‐expression network analysis (WGCNA). After the modules related to AR had been screened, the genes in the module were extracted for Gene Ontology and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment analysis, whereby the genes enriched in the KEGG pathway were regarded as the pathway‐genes. The DEGs in patients with AR were subsequently screened out from GSE19187, and the sensitive genes were identified in GSE18574 in connection with the allergen challenge. Two kinds of genes were compared with the pathway‐genes in order to screen the AR susceptibility genes. Receiver operating characteristic (ROC) curve was plotted to evaluate the capability of the susceptibility genes to distinguish the AR state. Based on the WGCNA in the GSE19187 data set, 10 co‐expression network modules were identified. The correlation analyses revealed that the yellow module was positively correlated with the disease state of AR. A total of 89 genes were found to be involved in the enrichment of the yellow module pathway. Four genes (CST1,SH2D1B,DPP4, and SLC5A5) were upregulated in AR and sensitive to allergen challenge, whose potentials were further confirmed by ROC curve. Taken together, CST1,SH2D1B,DPP4, and SLC5A5 are susceptibility genes to AR. John Wiley and Sons Inc. 2019-12-03 2020-01 /pmc/articles/PMC6951973/ /pubmed/31794148 http://dx.doi.org/10.1111/cts.12698 Text en © 2019 The Authors. Clinical and Translational Science published by Wiley Periodicals, Inc. on behalf of the American Society for Clinical Pharmacology and Therapeutics. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, 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 | Research Xue, Kai Yang, Jingpu Zhao, Yin Cheng, Jinzhang Wang, Zonggui Identification of Susceptibility Genes to Allergic Rhinitis by Gene Expression Data Sets |
title | Identification of Susceptibility Genes to Allergic Rhinitis by Gene Expression Data Sets |
title_full | Identification of Susceptibility Genes to Allergic Rhinitis by Gene Expression Data Sets |
title_fullStr | Identification of Susceptibility Genes to Allergic Rhinitis by Gene Expression Data Sets |
title_full_unstemmed | Identification of Susceptibility Genes to Allergic Rhinitis by Gene Expression Data Sets |
title_short | Identification of Susceptibility Genes to Allergic Rhinitis by Gene Expression Data Sets |
title_sort | identification of susceptibility genes to allergic rhinitis by gene expression data sets |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6951973/ https://www.ncbi.nlm.nih.gov/pubmed/31794148 http://dx.doi.org/10.1111/cts.12698 |
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