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Targeting the NRF2 pathway for disease modification in neurodegenerative diseases: mechanisms and therapeutic implications

Clara Mayer, Lluís Riera-Ponsati, Sakari Kauppinen, Henrik Klitgaard, Janine T. Erler*, Stine N. Hansen*

*Corresponding author for this work

Research output: Contribution to journalReviewpeer-review

47 Citations (Scopus)

Abstract

Neurodegenerative diseases constitute a global health issue and a major economic burden. They significantly impair both cognitive and motor functions, and their prevalence is expected to rise due to ageing societies and continuous population growth. Conventional therapies provide symptomatic relief, nevertheless, disease-modifying treatments that reduce or halt neuron death and malfunction are still largely unavailable. Amongst the common hallmarks of neurodegenerative diseases are protein aggregation, oxidative stress, neuroinflammation and mitochondrial dysfunction. Transcription factor nuclear factor-erythroid 2-related factor 2 (NRF2) constitutes a central regulator of cellular defense mechanisms, including the regulation of antioxidant, anti-inflammatory and mitochondrial pathways, making it a highly attractive therapeutic target for disease modification in neurodegenerative disorders. Here, we describe the role of NRF2 in the common hallmarks of neurodegeneration, review the current pharmacological interventions and their challenges in activating the NRF2 pathway, and present alternative therapeutic approaches for disease modification.

Original languageEnglish
Article number1437939
JournalFrontiers in Pharmacology
Volume15
ISSN1663-9812
DOIs
Publication statusPublished - 2024
Externally publishedYes

Bibliographical note

Publisher Copyright:
Copyright © 2024 Mayer, Riera-Ponsati, Kauppinen, Klitgaard, Erler and Hansen.

Keywords

  • BACH1
  • KEAP1
  • mitochondrial dysfunction
  • neurodegeneration
  • neuroinflammation
  • NRF2
  • oxidative stress

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