Bioinformatics-based screening and analysis of potential biomarkers in pediatric ulcerative colitis

Objective Bioinformatics analysis was performed to screen and identify the underlying gene biomarkers in pediatric ulcerative colitis (UC) patients.Methods GSE126124 dataset, the mRNA expression profile of inflammatory bowel disease, was downloaded from the gene expression omnibus (GEO) database. GE...

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Main Authors: ZOU Qiufeng, ZOU Jiaying, LI Lijuan, FANG Xiaoling, HUANG Wenjuan
Format: Article
Language:zho
Published: Editorial Office of New Medicine 2024-02-01
Series:Yixue xinzhi zazhi
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Online Access:https://yxxz.whuznhmedj.com/futureApi/storage/attach/2403/G1uz4OgqvEGjttYGil4JwqPROGXeAqFHRYNeWkQK.pdf
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author ZOU Qiufeng
ZOU Jiaying
LI Lijuan
FANG Xiaoling
HUANG Wenjuan
author_facet ZOU Qiufeng
ZOU Jiaying
LI Lijuan
FANG Xiaoling
HUANG Wenjuan
author_sort ZOU Qiufeng
collection DOAJ
description Objective Bioinformatics analysis was performed to screen and identify the underlying gene biomarkers in pediatric ulcerative colitis (UC) patients.Methods GSE126124 dataset, the mRNA expression profile of inflammatory bowel disease, was downloaded from the gene expression omnibus (GEO) database. GEO2R was utilized to obtain differentially expressed genes (DEGs) between pediatric ulcerative colitis tissues and corresponding normal tissues in the dataset. Functional and pathway enrichment analysis and protein-protein interaction analysis of DEGs were conducted using the DAVID and STRING database. The Cytoscape software was used to analyze protein-protein interaction network and hub genes. At last, the KEGG analyzed the biology and pathway enrichment of hub genes.Results A total of 153 DEGs were obtained, including 92 up-regulated and 61 down-regulated genes. Functional and pathway enrichment analysis showed that up-regulated DEGs were significantly enriched in the external stimulus, staphylococcus aureus infection and IL-17 signaling pathway. Functional and pathway enrichment analysis showed that down-regulated DEGs were significantly enriched in the transport, membrane composition and metabolic pathway. Furthermore, 10 DEGs were considered hub genes, including Cxcl1, Cxcl2, Cxcl10, Cxcr2, Il1rn, Fcgr3a, Cxcr1, S100a12, Ido1 and Ccl24. Pathway enrichment analysis showed that hub genes were significantly enriched in the chemokines, the interaction between viral proteins and cytokines and receptors, epithelial cells infected by Helicobacter pylori, IL-17 and TNF.Conclusion This research found 153 DEGs, in which 10 hub genes may play an important role in the occurrence and development of pediatric UC.
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spelling doaj-art-57076bf94cb44e9d96fe14bc552701f52025-08-20T02:00:01ZzhoEditorial Office of New MedicineYixue xinzhi zazhi1004-55112024-02-0134214915610.12173/j.issn.1004-5511.2023020366442Bioinformatics-based screening and analysis of potential biomarkers in pediatric ulcerative colitisZOU QiufengZOU JiayingLI LijuanFANG XiaolingHUANG WenjuanObjective Bioinformatics analysis was performed to screen and identify the underlying gene biomarkers in pediatric ulcerative colitis (UC) patients.Methods GSE126124 dataset, the mRNA expression profile of inflammatory bowel disease, was downloaded from the gene expression omnibus (GEO) database. GEO2R was utilized to obtain differentially expressed genes (DEGs) between pediatric ulcerative colitis tissues and corresponding normal tissues in the dataset. Functional and pathway enrichment analysis and protein-protein interaction analysis of DEGs were conducted using the DAVID and STRING database. The Cytoscape software was used to analyze protein-protein interaction network and hub genes. At last, the KEGG analyzed the biology and pathway enrichment of hub genes.Results A total of 153 DEGs were obtained, including 92 up-regulated and 61 down-regulated genes. Functional and pathway enrichment analysis showed that up-regulated DEGs were significantly enriched in the external stimulus, staphylococcus aureus infection and IL-17 signaling pathway. Functional and pathway enrichment analysis showed that down-regulated DEGs were significantly enriched in the transport, membrane composition and metabolic pathway. Furthermore, 10 DEGs were considered hub genes, including Cxcl1, Cxcl2, Cxcl10, Cxcr2, Il1rn, Fcgr3a, Cxcr1, S100a12, Ido1 and Ccl24. Pathway enrichment analysis showed that hub genes were significantly enriched in the chemokines, the interaction between viral proteins and cytokines and receptors, epithelial cells infected by Helicobacter pylori, IL-17 and TNF.Conclusion This research found 153 DEGs, in which 10 hub genes may play an important role in the occurrence and development of pediatric UC.https://yxxz.whuznhmedj.com/futureApi/storage/attach/2403/G1uz4OgqvEGjttYGil4JwqPROGXeAqFHRYNeWkQK.pdfpediatriculcerative colitisgenebioinformaticsbiomarkers
spellingShingle ZOU Qiufeng
ZOU Jiaying
LI Lijuan
FANG Xiaoling
HUANG Wenjuan
Bioinformatics-based screening and analysis of potential biomarkers in pediatric ulcerative colitis
Yixue xinzhi zazhi
pediatric
ulcerative colitis
gene
bioinformatics
biomarkers
title Bioinformatics-based screening and analysis of potential biomarkers in pediatric ulcerative colitis
title_full Bioinformatics-based screening and analysis of potential biomarkers in pediatric ulcerative colitis
title_fullStr Bioinformatics-based screening and analysis of potential biomarkers in pediatric ulcerative colitis
title_full_unstemmed Bioinformatics-based screening and analysis of potential biomarkers in pediatric ulcerative colitis
title_short Bioinformatics-based screening and analysis of potential biomarkers in pediatric ulcerative colitis
title_sort bioinformatics based screening and analysis of potential biomarkers in pediatric ulcerative colitis
topic pediatric
ulcerative colitis
gene
bioinformatics
biomarkers
url https://yxxz.whuznhmedj.com/futureApi/storage/attach/2403/G1uz4OgqvEGjttYGil4JwqPROGXeAqFHRYNeWkQK.pdf
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AT zoujiaying bioinformaticsbasedscreeningandanalysisofpotentialbiomarkersinpediatriculcerativecolitis
AT lilijuan bioinformaticsbasedscreeningandanalysisofpotentialbiomarkersinpediatriculcerativecolitis
AT fangxiaoling bioinformaticsbasedscreeningandanalysisofpotentialbiomarkersinpediatriculcerativecolitis
AT huangwenjuan bioinformaticsbasedscreeningandanalysisofpotentialbiomarkersinpediatriculcerativecolitis