Correction of RNA-Binding Protein CUGBP1 and GSK3β Signaling as Therapeutic Approach for Congenital and Adult Myotonic Dystrophy Type 1

Int J Mol Sci. 2019 Dec 21;21(1):94. doi: 10.3390/ijms21010094.

Abstract

Myotonic dystrophy type 1 (DM1) is a complex genetic disease affecting many tissues. DM1 is caused by an expansion of CTG repeats in the 3'-UTR of the DMPK gene. The mechanistic studies of DM1 suggested that DMPK mRNA, containing expanded CUG repeats, is a major therapeutic target in DM1. Therefore, the removal of the toxic RNA became a primary focus of the therapeutic development in DM1 during the last decade. However, a cure for this devastating disease has not been found. Whereas the degradation of toxic RNA remains a preferential approach for the reduction of DM1 pathology, other approaches targeting early toxic events downstream of the mutant RNA could be also considered. In this review, we discuss the beneficial role of the restoring of the RNA-binding protein, CUGBP1/CELF1, in the correction of DM1 pathology. It has been recently found that the normalization of CUGBP1 activity with the inhibitors of GSK3 has a positive effect on the reduction of skeletal muscle and CNS pathologies in DM1 mouse models. Surprisingly, the inhibitor of GSK3, tideglusib also reduced the toxic CUG-containing RNA. Thus, the development of the therapeutics, based on the correction of the GSK3β-CUGBP1 pathway, is a promising option for this complex disease.

Keywords: CUGBP1; GSK3 inhibitors; GSK3β signaling; congenital myotonic dystrophy; myotonic dystrophy.

Publication types

  • Review

MeSH terms

  • Animals
  • CELF1 Protein / metabolism*
  • Enzyme Inhibitors / therapeutic use
  • Glycogen Synthase Kinase 3 beta / antagonists & inhibitors*
  • Glycogen Synthase Kinase 3 beta / metabolism
  • Humans
  • Myotonic Dystrophy / drug therapy*
  • Myotonic Dystrophy / genetics
  • Myotonic Dystrophy / metabolism
  • Myotonin-Protein Kinase / genetics*
  • Myotonin-Protein Kinase / metabolism
  • Signal Transduction
  • Thiadiazoles / therapeutic use

Substances

  • CELF1 Protein
  • Enzyme Inhibitors
  • Thiadiazoles
  • Glycogen Synthase Kinase 3 beta
  • Myotonin-Protein Kinase
  • tideglusib