Recent Advances in Understanding Nrf2 Agonism and Its Potential Clinical Application to Metabolic and Inflammatory Diseases.
Min-Ji KimJae-Han JeonPublished in: International journal of molecular sciences (2022)
Oxidative stress is a major component of cell damage and cell fat, and as such, it occupies a central position in the pathogenesis of metabolic disease. Nuclear factor-erythroid-derived 2-related factor 2 (Nrf2), a key transcription factor that coordinates expression of genes encoding antioxidant and detoxifying enzymes, is regulated primarily by Kelch-like ECH-associated protein 1 (Keap1). However, involvement of the Keap1-Nrf2 pathway in tissue and organism homeostasis goes far beyond protection from cellular stress. In this review, we focus on evidence for Nrf2 pathway dysfunction during development of several metabolic/inflammatory disorders, including diabetes and diabetic complications, obesity, inflammatory bowel disease, and autoimmune diseases. We also review the beneficial role of current molecular Nrf2 agonists and summarize their use in ongoing clinical trials. We conclude that Nrf2 is a promising target for regulation of numerous diseases associated with oxidative stress and inflammation. However, more studies are needed to explore the role of Nrf2 in the pathogenesis of metabolic/inflammatory diseases and to review safety implications before therapeutic use in clinical practice.
Keyphrases
- oxidative stress
- diabetic rats
- dna damage
- ischemia reperfusion injury
- induced apoptosis
- transcription factor
- type diabetes
- clinical trial
- nuclear factor
- single cell
- metabolic syndrome
- toll like receptor
- poor prognosis
- adipose tissue
- insulin resistance
- cell therapy
- immune response
- gene expression
- weight loss
- dna methylation
- mesenchymal stem cells
- randomized controlled trial
- small molecule
- signaling pathway
- glycemic control
- protein protein
- heat shock protein
- endoplasmic reticulum stress
- wound healing