Idiopathic pulmonary fibrosis: Pathogenesis and the emerging role of long non-coding RNAs

Marina R. Hadjicharalambous, Mark A. Lindsay

Research output: Contribution to journalReview articlepeer-review

43 Citations (SciVal)


Idiopathic pulmonary fibrosis (IPF) is a progressive chronic disease characterized by excessing scarring of the lungs leading to irreversible decline in lung function. The aetiology and pathogenesis of the disease are still unclear, although lung fibroblast and epithelial cell activation, as well as the secretion of fibrotic and inflammatory mediators, have been strongly associated with the development and progression of IPF. Significantly, long non-coding RNAs (lncRNAs) are emerging as modulators of multiple biological processes, although their function and mechanism of action in IPF is poorly understood. LncRNAs have been shown to be important regulators of several diseases and their aberrant expression has been linked to the pathophysiology of fibrosis including IPF. This review will provide an overview of this emerging role of lncRNAs in the development of IPF.

Original languageEnglish
Article number524
JournalInternational Journal of Molecular Sciences
Issue number2
Publication statusPublished - 14 Jan 2020


  • Fibrosis
  • IPF
  • lncRNAs
  • Long non-coding RNAs
  • Lung

ASJC Scopus subject areas

  • Catalysis
  • Molecular Biology
  • Spectroscopy
  • Computer Science Applications
  • Physical and Theoretical Chemistry
  • Organic Chemistry
  • Inorganic Chemistry


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