Oxidative stress in DNA repeat expansion disorders: A focus on NRF2 signaling involvement

P. La Rosa, S. Petrillo, E.S. Bertini, F. Piemonte

Research output: Contribution to journalArticlepeer-review

Abstract

DNA repeat expansion disorders are a group of neuromuscular and neurodegenerative diseases that arise from the inheritance of long tracts of nucleotide repetitions, located in the regulatory region, introns, or inside the coding sequence of a gene. Although loss of protein expression and/or the gain of function of its transcribed mRNA or translated product represent the major pathogenic effect of these pathologies, mitochondrial dysfunction and imbalance in redox homeostasis are reported as common features in these disorders, deeply affecting their severity and progression. In this review, we examine the role that the redox imbalance plays in the pathological mechanisms of DNA expansion disorders and the recent advances on antioxidant treatments, particularly focusing on the expression and the activity of the transcription factor NRF2, the main cellular regulator of the antioxidant response. © 2020 by the authors. Licensee MDPI, Basel, Switzerland.
Original languageEnglish
JournalBiomolecules
Volume10
Issue number5
DOIs
Publication statusPublished - 2020

Keywords

  • DNA repeat expansion disorders
  • Fragile X syndrome
  • Friedreich’s ataxia
  • FXTAS
  • Huntington’s disease
  • Myotonic dystrophy
  • NRF2
  • Oxidative stress
  • Spinal and bulbar muscular atrophy
  • Spinocerebellar ataxia
  • transcription factor Nrf2
  • antioxidant responsive element
  • cell function
  • degenerative disease
  • DNA repeat expansion disorder
  • fragile x associated tremor ataxia syndrome
  • fragile X syndrome
  • Friedreich ataxia
  • genetic disorder
  • human
  • Huntington chorea
  • Kennedy disease
  • loss of function mutation
  • myotonic dystrophy
  • neuromuscular disease
  • neuropathology
  • nonhuman
  • oxidation reduction state
  • oxidative stress
  • protein expression
  • Review
  • signal transduction
  • spinocerebellar degeneration
  • transcription regulation

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