Identification of key genes and microRNAs for multiple sclerosis using bioinformatics analysis

Medicine (Baltimore). 2021 Dec 3;100(48):e27667. doi: 10.1097/MD.0000000000027667.

Abstract

To better understand the molecular mechanism underlying the pathogenesis of multiple sclerosis (MS), we aimed to identify the key genes and microRNAs (miRNA) associated with MS and analyze their interactions. Differentially expressed genes (DEGs) and miRNAs (DEMs) based on the gene miRNA dataset GSE17846 and mRNA dataset GSE21942 were determined using R software. Next, we performed functional enrichment analysis and constructed a protein-protein interaction network. Data validation was performed to ensure the reliability of hub genes. The miRNA-mRNA regulatory network was constructed. In total, 47 DEMs and 843 DEGs were identified. Protein-protein interaction network analysis identified several hub genes, including JUN, FPR2, AKT1, POLR2L, LYZ, CXCL8, HBB, CST3, CTSZ, and MMP9, especially LYZ and CXCL8. We constructed an miRNA-mRNA regulatory network and found that hsa-miR-142-3p, hsa-miR-107, hsa-miR-140-5p, and hsa-miR-613 were the most important miRNAs. This study reveals some key genes and miRNAs that may be involved in the pathogenesis of MS, providing potential targets for the diagnosis and treatment of MS.

MeSH terms

  • Computational Biology*
  • Gene Expression Profiling
  • Gene Regulatory Networks
  • Humans
  • MicroRNAs / genetics*
  • Multiple Sclerosis / genetics*
  • Multiple Sclerosis / pathology
  • RNA, Messenger / genetics
  • Reproducibility of Results

Substances

  • MIRN613 microRNA, human
  • MicroRNAs
  • Mirn140 microRNA, human
  • RNA, Messenger