Non-Coding Ribonucleic Acids as Diagnostic and Therapeutic Targets in Cardiac Fibrosis

Curr Heart Fail Rep. 2024 Jun;21(3):262-275. doi: 10.1007/s11897-024-00653-1. Epub 2024 Mar 15.

Abstract

Purpose of review: Cardiac fibrosis is a crucial juncture following cardiac injury and a precursor for many clinical heart disease manifestations. Epigenetic modulators, particularly non-coding RNAs (ncRNAs), are gaining prominence as diagnostic and therapeutic tools.

Recent findings: miRNAs are short linear RNA molecules involved in post-transcriptional regulation; lncRNAs and circRNAs are RNA sequences greater than 200 nucleotides that also play roles in regulating gene expression through a variety of mechanisms including miRNA sponging, direct interaction with mRNA, providing protein scaffolding, and encoding their own products. NcRNAs have the capacity to regulate one another and form sophisticated regulatory networks. The individual roles and disease relevance of miRNAs, lncRNAs, and circRNAs to cardiac fibrosis have been increasingly well described, though the complexity of their interrelationships, regulatory dynamics, and context-specific roles needs further elucidation. This review provides an overview of select ncRNAs relevant in cardiac fibrosis as a surrogate for many cardiac disease states with a focus on crosstalk and regulatory networks, variable actions among different disease states, and the clinical implications thereof. Further, the clinical feasibility of diagnostic and therapeutic applications as well as the strategies underway to advance ncRNA theranostics is explored.

Keywords: Cardiac fibrosis; Circular RNA (circRNA); Epigenetic modulation; Long non-coding RNA (lncRNA); Non-coding RNAs; Regulatory networks; microRNA (miRNA).

Publication types

  • Review
  • Research Support, Non-U.S. Gov't
  • Research Support, N.I.H., Extramural

MeSH terms

  • Biomarkers / metabolism
  • Fibrosis* / genetics
  • Gene Expression Regulation
  • Heart Diseases / diagnosis
  • Heart Diseases / genetics
  • Humans
  • MicroRNAs / genetics
  • Myocardium / metabolism
  • Myocardium / pathology
  • RNA, Long Noncoding / genetics
  • RNA, Untranslated* / genetics

Substances

  • RNA, Untranslated
  • RNA, Long Noncoding
  • MicroRNAs
  • Biomarkers