Identification of miRNAs and their potential effects on multiple sclerosis related pathways using ın silico analysis

Burcin Erkal1, Senay Vural Korkut1

  • 1Department of Molecular Biology and Genetics, Yildiz Technical University, Istanbul, Turkey.

Abstract

Insights

MicroRNAs (miRNAs) are key regulators of gene expression and potential biomarkers for multiple sclerosis (MS). This study identified crucial miRNAs and pathways involved in MS pathogenesis, offering new therapeutic targets.

Area of Science:

  • Genomics
  • Molecular Biology
  • Biomarker Discovery

Background:

  • MicroRNAs (miRNAs) post-transcriptionally regulate gene expression, influencing health and disease pathways.
  • miRNAs show potential as diagnostic, prognostic, and therapeutic biomarkers for immune and nervous system diseases, including multiple sclerosis (MS).

Purpose of the Study:

  • To evaluate MS-related microRNAs (miRNAs) and their impact on associated biological pathways.
  • To identify potential biomarkers and therapeutic targets for understanding MS pathogenesis.

Main Methods:

  • Differentially expressed miRNAs were identified from peripheral blood samples using NCBI GEO Datasets and GEO2R.
  • Pathway analysis was conducted using miRNet, miRWalk, DIANA mirpath, and KEGG.
  • Target gene and protein-protein interaction analyses were performed using STRING and GeneMANIA.

Main Results:

  • Twelve common miRNAs were identified, with four significantly associated with MS-related immune and neural signaling pathways.
  • Key pathways implicated include neurotrophin, JAK-STAT, B cell receptor, ErbB, MAPK, Fc gamma R-mediated phagocytosis, Chemokine, and T cell receptor signaling.
  • Target gene analysis revealed MAPK1, PIK3CD, PIK3R1, PIK3R2, PIK3R3, PIK3R5, AKT2, SOS2, and RAF1, with significant overlap in the PI3K-Akt signaling pathway.

Conclusions:

  • This study elucidates MS-related miRNAs and their functional pathways.
  • The findings provide insights into MS pathogenesis and suggest novel tools for therapeutic development.