MicroRNAs overexpressed in Crohn's disease and their interactions with mechanisms of epigenetic regulation explain novel aspects of Crohn's disease pathogenesis

Clin Epigenetics. 2021 Feb 18;13(1):39. doi: 10.1186/s13148-021-01022-8.

Abstract

Background: In this review, we were interested to identify the wide universe of enzymes associated with epigenetic modifications, whose gene expression is regulated by miRNAs with a high relative abundance in Crohn's disease (CD) affected tissues, with the aim to determine their impact in the pathogenesis and evolution of the disease.

Methods: We used HMDD and Bibliometrix R-package in order to identify the miRNAs overexpressed in CD. The identified enzymes associated with epigenetic mechanisms and post-translational modifications, regulated by miRNAs upregulated in CD, were analyzed using String v11 database.

Results: We found 190 miRNAs with great abundance in patients with CD, of which 26 miRNAs regulate the gene expression of enzymes known to catalyze epigenetic modifications involved in essentials pathophysiological processes, such as chromatin architecture reorganization, immune response regulation including CD4+ T cells polarization, integrity of gut mucosa, gut microbiota composition and tumorigenesis.

Conclusion: The integrated analysis of miRNAs with a high relative abundance in patients with CD showed a combined and superimposed gene expression regulation of enzymes associated with relevant epigenetic mechanisms and that could explain, in part, the pathogenesis of CD.

Keywords: Crohn’s disease; Epigenetic mechanisms; MicroRNA; Post-translational modifications; T cells.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • CD4-Positive T-Lymphocytes / metabolism
  • Chromatin Assembly and Disassembly / genetics
  • CpG Islands
  • Crohn Disease / enzymology*
  • Crohn Disease / genetics*
  • Crohn Disease / physiopathology
  • DNA Methylation
  • Epigenesis, Genetic
  • Gene Expression Regulation
  • Humans
  • Immunity / genetics
  • MicroRNAs / genetics*
  • Protein Interaction Maps / genetics
  • Protein Processing, Post-Translational / genetics

Substances

  • MicroRNAs