Differentially expressed genes of ulcerative colitis and associated microRNAs based on bioinformatics analysis
- VernacularTitle:基于生物信息学分析溃疡性结肠炎的差异表达基因和相关微小RNA
- Author:
Shengnan WU
1
;
Huanyu JIANG
;
Haoran CHEN
;
Xinyao WANG
;
Jiahui WU
;
Luqi WANG
Author Information
- Keywords: ulcerative colitis; weighted gene co-expression network; miRNA-gene regulatory networks; bioinformatics
- From: Journal of Clinical Medicine in Practice 2024;28(1):48-55
- CountryChina
- Language:Chinese
- Abstract: Objective To analyze differentially expressed genes and potential microRNA(miR-NAs)with diagnostic and therapeutic potential in ulcerative colitis(UC)based on bioinformatics.Methods The chip raw data in GEO database was screened by weighted gene coexpression network analysis.UC related differentially expressed genes were obtained for enrichment analysis.Potential miRNAs associated with differentially expressed genes were predicted based on key genes,and gene-miRNA regulatory networks were constructed.Results A total of 277 differentially expressed genes were screened,of which 200 genes were up-regulated and 77 genes were down-regulated.Gene set en-richment analysis(GSEA)showed that the main enrichment pathways were neuroactive ligand-receptor interaction,leishmania infection,prion disease and electrocardiogram receptor interaction.The results of gene ontology(GO)analysis showed that it was mainly involved in chemokine activity,heparin binding as well as chemokine receptor binding and other items.The Kyoto Encyclopedia of Genes and Genomes(KEGG)analysis showed that the main enrichment pathways were cytokine receptor interaction pathway,phosphatidylinositol-3 kinase/protein kinase B(PI3K-AKT)signaling pathway,chemokine signaling pathway as well as nuclear transcription factor kappa B(NF-κB)signaling pathway and other pathway.A total of 10 hub genes were screened:C-X-C chemokine ligand 8(CXCL8),Toll-like receptor 2(TLR2),intercellular adhesion molecule-1(ICAM-1),selectin L(SELL),C-X-C chemokine receptor type 4(CXCR4),cytotoxic T lymphocyte associated antigen 4(CTLA4),clus-ter of differentiation 69(CD69),and Biglycan(BGN),C-X-C chemokine ligand 13(CXCL13),tissue inhibitor of metalloproteinases 1(TIMP1).A total of 12 potentially key miRNAs were identi-fied,they were respectively hsa-mir-335-5p,hsa-mir-146a-5p,hsa-mir-92a-3p,hsa-mir-155-5p,hsa-mir-26b-5p,hsa-mir-4426,hsa-mir-4462b,hsa-mir-4647,hsa-mir-32-5p,hsa-mir-92b-3p,hsa-mir-98-5p and hsa-mir-93-5p,respectively.Conclusion In this study,a total of 277 differen-tially expressed genes are screened for possible involvement in the development of UC,and 10 hub genes and 12 miRNAs are identified as possible biomarkers for UC.
