Muscle miRNAome shows suppression of chronic inflammatory miRNAs with both prednisone and vamorolone

Physiol Genomics. 2018 Sep 1;50(9):735-745. doi: 10.1152/physiolgenomics.00134.2017. Epub 2018 Jun 8.

Abstract

Corticosteroids are highly prescribed and effective anti-inflammatory drugs but the burden of side effects with chronic use significantly detracts from patient quality of life, particularly in children. Developing safer steroids amenable to long-term use is an important goal for treatment of chronic inflammatory diseases such as Duchenne muscular dystrophy (DMD). We have developed vamorolone (VBP15), a first-in-class dissociative glucocorticoid receptor (GR) ligand that shows the anti-inflammatory efficacy of corticosteroids without key steroid side effects in animal models. miRNAs are increasingly recognized as key regulators of inflammatory responses. To define effects of prednisolone and vamorolone on the muscle miRNAome, we performed a preclinical discovery study in the mdx mouse model of DMD. miRNAs associated with inflammation were highly elevated in mdx muscle. Both vamorolone and prednisolone returned these toward wild-type levels (miR-142-5p, miR-142-3p, miR-146a, miR-301a, miR-324-3p, miR-455-5p, miR-455-3p, miR-497, miR-652). Effects of vamorolone were largely limited to reduction of proinflammatory miRNAs. In contrast, prednisolone activated a separate group of miRNAs associated with steroid side effects and a noncoding RNA cluster homologous to human chromosome 14q32. Effects were validated for inflammatory miRNAs in a second, independent preclinical study. For the anti-inflammatory miRNA signature, bioinformatic analyses showed all of these miRNAs are directly regulated by, or in turn activate, the inflammatory transcription factor NF-κB. Moving forward miR-146a and miR-142 are of particular interest as biomarkers or novel drug targets. These data validate NF-κB signaling as a target of dissociative GR-ligand efficacy in vivo and provide new insight into miRNA signaling in chronic inflammation.

Keywords: Duchenne muscular dystrophy; inflammation; miRNA; muscle; steroids.

Publication types

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

MeSH terms

  • Animals
  • Base Sequence
  • Chronic Disease
  • Disease Models, Animal
  • Gene Expression Regulation / drug effects
  • Inflammation / genetics*
  • Mice, Inbred C57BL
  • Mice, Inbred mdx
  • MicroRNAs / genetics*
  • MicroRNAs / metabolism
  • Models, Biological
  • Muscles / drug effects
  • Muscles / metabolism*
  • Muscles / pathology
  • Muscular Dystrophy, Duchenne / genetics
  • NF-kappa B / metabolism
  • Prednisone / pharmacology*
  • Pregnadienediols / pharmacology*
  • Promoter Regions, Genetic / genetics
  • Receptors, Glucocorticoid / metabolism
  • Reproducibility of Results
  • Signal Transduction

Substances

  • MicroRNAs
  • NF-kappa B
  • Pregnadienediols
  • Receptors, Glucocorticoid
  • VBP15 compound
  • Prednisone