A randomized controlled trial of inhaled corticosteroids (ICS) on markers of epithelial-mesenchymal transition (EMT) in large airway samples in COPD: an exploratory proof of concept study

Int J Chron Obstruct Pulmon Dis. 2014 May 27:9:533-42. doi: 10.2147/COPD.S63911. eCollection 2014.

Abstract

Background: We recently reported that epithelial-mesenchymal transition (EMT) is active in the airways in chronic obstructive pulmonary disease (COPD), suggesting presence of an active profibrotic and promalignant stroma. With no data available on potential treatment effects, we undertook a blinded analysis of inhaled corticosteroids (ICS) effects versus placebo on EMT markers in previously obtained endobronchial biopsies in COPD patients, as a "proof of concept" study.

Methods: Assessment of the effects of inhaled fluticasone propionate (FP; 500 μg twice daily for 6 months) versus placebo in 34 COPD patients (23 on fluticasone propionate and eleven on placebo). The end points were epidermal growth factor receptor (EGFR; marker of epithelial activation) and the biomarkers of EMT: reticular basement membrane (Rbm) fragmentation ("hallmark" structural marker), matrix metalloproteinase-9 (MMP-9) cell expression, and S100A4 expression in basal epithelial and Rbm cells (mesenchymal transition markers).

Results: Epithelial activation, "clefts/fragmentation" in the Rbm, and changes in the other biomarkers all regressed on ICS, at or close to conventional levels of statistical significance. From these data, we have been able to nominate primary and secondary end points and develop power calculations that would be applicable to a definitive prospective study.

Conclusion: Although only a pilot "proof of concept" study, this trial provided strong suggestive support for an anti-EMT effect of ICS in COPD airways. A larger and fully powered prospective study is now indicated as this issue is likely to be extremely important. Such studies may clarify the links between ICS use and better clinical outcomes and protection against lung cancer in COPD.

Keywords: EGFR; MMP-9; S100A4; lung cancer; pilot trial; reticular basement membrane.

Publication types

  • Multicenter Study
  • Randomized Controlled Trial

MeSH terms

  • Administration, Inhalation
  • Adrenal Cortex Hormones / administration & dosage*
  • Adult
  • Aged
  • Airway Remodeling / drug effects*
  • Androstadienes / administration & dosage*
  • Australia
  • Biomarkers / metabolism
  • Double-Blind Method
  • Drug Administration Schedule
  • Epithelial-Mesenchymal Transition / drug effects*
  • ErbB Receptors / metabolism
  • Female
  • Fluticasone
  • Humans
  • Lung / drug effects*
  • Lung / metabolism
  • Lung / pathology
  • Male
  • Matrix Metalloproteinase 9 / metabolism
  • Middle Aged
  • Pilot Projects
  • Prospective Studies
  • Pulmonary Disease, Chronic Obstructive / diagnosis
  • Pulmonary Disease, Chronic Obstructive / drug therapy*
  • Pulmonary Disease, Chronic Obstructive / metabolism
  • S100 Calcium-Binding Protein A4
  • S100 Proteins / metabolism
  • Treatment Outcome

Substances

  • Adrenal Cortex Hormones
  • Androstadienes
  • Biomarkers
  • S100 Calcium-Binding Protein A4
  • S100 Proteins
  • S100A4 protein, human
  • Fluticasone
  • EGFR protein, human
  • ErbB Receptors
  • MMP9 protein, human
  • Matrix Metalloproteinase 9

Associated data

  • ANZCTR/ACTRN12612001111864