Identification of key genes in allergic rhinitis by bioinformatics analysis

Objective This study aimed to explore the potential molecular mechanism of allergic rhinitis (AR) and identify gene signatures by analyzing microarray data using bioinformatics methods. Methods The dataset GSE19187 was used to screen differentially expressed genes (DEGs) between samples from patient...

Full description

Bibliographic Details
Main Authors: Yunfei Zhang, Yue Huang, Wen-xia Chen, Zheng-min Xu
Format: Article
Language:English
Published: SAGE Publishing 2021-07-01
Series:Journal of International Medical Research
Online Access:https://doi.org/10.1177/03000605211029521
id doaj-1e4ac90f7c7d47a6a6f6c758ed2e87d2
record_format Article
spelling doaj-1e4ac90f7c7d47a6a6f6c758ed2e87d22021-07-31T23:03:30ZengSAGE PublishingJournal of International Medical Research1473-23002021-07-014910.1177/03000605211029521Identification of key genes in allergic rhinitis by bioinformatics analysisYunfei ZhangYue HuangWen-xia ChenZheng-min XuObjective This study aimed to explore the potential molecular mechanism of allergic rhinitis (AR) and identify gene signatures by analyzing microarray data using bioinformatics methods. Methods The dataset GSE19187 was used to screen differentially expressed genes (DEGs) between samples from patients with AR and healthy controls. Gene ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analyses were applied for the DEGs. Subsequently, a protein–protein interaction (PPI) network was constructed to identify hub genes. GSE44037 and GSE43523 datasets were screened to validate critical genes. Results A total of 156 DEGs were identified. GO analysis verified that the DEGs were enriched in antigen processing and presentation, the immune response, and antigen binding. KEGG analysis demonstrated that the DEGs were enriched in Staphylococcus aureus infection, rheumatoid arthritis, and allograft rejection. PPI network and module analysis predicted seven hub genes, of which six ( CD44 , HLA-DPA1 , HLA-DRB1 , HLA-DRB5 , MUC5B , and CD274 ) were identified in the validation dataset. Conclusions Our findings suggest that hub genes play important roles in the development of AR.https://doi.org/10.1177/03000605211029521
collection DOAJ
language English
format Article
sources DOAJ
author Yunfei Zhang
Yue Huang
Wen-xia Chen
Zheng-min Xu
spellingShingle Yunfei Zhang
Yue Huang
Wen-xia Chen
Zheng-min Xu
Identification of key genes in allergic rhinitis by bioinformatics analysis
Journal of International Medical Research
author_facet Yunfei Zhang
Yue Huang
Wen-xia Chen
Zheng-min Xu
author_sort Yunfei Zhang
title Identification of key genes in allergic rhinitis by bioinformatics analysis
title_short Identification of key genes in allergic rhinitis by bioinformatics analysis
title_full Identification of key genes in allergic rhinitis by bioinformatics analysis
title_fullStr Identification of key genes in allergic rhinitis by bioinformatics analysis
title_full_unstemmed Identification of key genes in allergic rhinitis by bioinformatics analysis
title_sort identification of key genes in allergic rhinitis by bioinformatics analysis
publisher SAGE Publishing
series Journal of International Medical Research
issn 1473-2300
publishDate 2021-07-01
description Objective This study aimed to explore the potential molecular mechanism of allergic rhinitis (AR) and identify gene signatures by analyzing microarray data using bioinformatics methods. Methods The dataset GSE19187 was used to screen differentially expressed genes (DEGs) between samples from patients with AR and healthy controls. Gene ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analyses were applied for the DEGs. Subsequently, a protein–protein interaction (PPI) network was constructed to identify hub genes. GSE44037 and GSE43523 datasets were screened to validate critical genes. Results A total of 156 DEGs were identified. GO analysis verified that the DEGs were enriched in antigen processing and presentation, the immune response, and antigen binding. KEGG analysis demonstrated that the DEGs were enriched in Staphylococcus aureus infection, rheumatoid arthritis, and allograft rejection. PPI network and module analysis predicted seven hub genes, of which six ( CD44 , HLA-DPA1 , HLA-DRB1 , HLA-DRB5 , MUC5B , and CD274 ) were identified in the validation dataset. Conclusions Our findings suggest that hub genes play important roles in the development of AR.
url https://doi.org/10.1177/03000605211029521
work_keys_str_mv AT yunfeizhang identificationofkeygenesinallergicrhinitisbybioinformaticsanalysis
AT yuehuang identificationofkeygenesinallergicrhinitisbybioinformaticsanalysis
AT wenxiachen identificationofkeygenesinallergicrhinitisbybioinformaticsanalysis
AT zhengminxu identificationofkeygenesinallergicrhinitisbybioinformaticsanalysis
_version_ 1721246383791407104