MiRNA, a New Treatment Strategy for Pulmonary Fibrosis

Curr Drug Targets. 2021;22(7):793-802. doi: 10.2174/1874609813666200928141822.

Abstract

Pulmonary fibrosis (PF) is the most common chronic, progressive interstitial lung disease, mainly occurring in the elderly, with a median survival of 2-4 years after diagnosis. Its high mortality rate attributes to the delay in diagnosis due to its generic symptoms, and more importantly, to the lack of effective treatments. MicroRNAs (miRNAs) are a class of small non-coding RNAs that are involved in many essential cellular processes, including extracellular matrix remodeling, alveolar epithelial cell apoptosis, epithelial-mesenchymal transition, etc. We summarized the dysregulated miRNAs in TGF-β signaling pathway-mediated PF in recent years with dual effects, such as anti-fibrotic let-7 family and pro-fibrotic miR-21 members. Therefore, this review will set out the latest application of miRNAs to provide a new direction for PF treatment.

Keywords: Pulmonary fibrosis; epithelial-mesenchymal transition; extracellular matrix; microRNAs; pro-fibrotic; transforming growth factor-β.

Publication types

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

MeSH terms

  • Humans
  • MicroRNAs* / genetics
  • MicroRNAs* / therapeutic use
  • Pulmonary Fibrosis* / therapy
  • Signal Transduction
  • Transforming Growth Factor beta

Substances

  • MIRN21 microRNA, human
  • MicroRNAs
  • Transforming Growth Factor beta
  • mirnlet7 microRNA, human