Genetics and prospective therapeutic targets for Sjögren-Larsson Syndrome.
William B RizzoPublished in: Expert opinion on orphan drugs (2016)
The most promising pharmacologic approach to SLS involves blocking the formation of potentially harmful fatty aldehyde adducts using aldehyde scavenging drugs, currently in phase 2 clinical trials. Other approaches needing further investigation include: 1) ALDH-specific activator drugs and PPAR-α agonists to increase mutant FALDH activity; 2) inhibitors of the JNK phosphorylation cascade; 3) antioxidants to decrease aldehyde load; 4) dietary lipid modification; and 5) gene therapy.
Keyphrases
- gene therapy
- clinical trial
- fatty acid
- signaling pathway
- cell death
- nuclear factor
- insulin resistance
- disease activity
- randomized controlled trial
- type diabetes
- immune response
- adipose tissue
- systemic lupus erythematosus
- toll like receptor
- rheumatoid arthritis
- skeletal muscle
- induced apoptosis
- phase ii
- open label
- study protocol
- endoplasmic reticulum stress