PUBLICATION
Dasatinib as a treatment for Duchenne muscular dystrophy
- Authors
- Lipscomb, L., Piggott, R.W., Emmerson, T., Winder, S.J.
- ID
- ZDB-PUB-151126-3
- Date
- 2016
- Source
- Human molecular genetics 25(2): 266-74 (Journal)
- Registered Authors
- Keywords
- Dasatinib, Duchenne muscular dystrophy, dystroglycan, proteasome, tyrosine phosphorylation, ubiquitination, zebrafish
- MeSH Terms
-
- Animals
- Dasatinib/therapeutic use*
- Dystroglycans/metabolism*
- Muscles/drug effects
- Muscles/metabolism
- Muscular Dystrophy, Animal/drug therapy*
- Muscular Dystrophy, Animal/metabolism
- Muscular Dystrophy, Duchenne/drug therapy*
- Muscular Dystrophy, Duchenne/metabolism
- Phosphorylation
- Protein Kinase Inhibitors/therapeutic use*
- Proteolysis
- Zebrafish/genetics
- Zebrafish/metabolism
- Zebrafish Proteins/metabolism
- src-Family Kinases/antagonists & inhibitors*
- src-Family Kinases/metabolism
- PubMed
- 26604135 Full text @ Hum. Mol. Genet.
Citation
Lipscomb, L., Piggott, R.W., Emmerson, T., Winder, S.J. (2016) Dasatinib as a treatment for Duchenne muscular dystrophy. Human molecular genetics. 25(2):266-74.
Abstract
Identification of a systemically acting and universal small molecule therapy for Duchenne muscular dystrophy would be an enormous advance for this condition. Based on evidence gained from studies on mouse genetic models we have identified tyrosine phosphorylation and degradation of β-dystroglycan as a key event in the aetiology of Duchenne muscular dystrophy. Thus preventing tyrosine phosphorylation and degradation of β-dystroglycan presents itself as a potential therapeutic strategy. Using the dystrophic sapje zebrafish we have investigated the use of tyrosine kinase and other inhibitors to treat the dystrophic symptoms in this model of Duchenne muscular dystrophy. Dasatinib, a potent and specific Src tyrosine kinase inhibitor was found to decrease the levels of β-dystroglycan phosphorylation on tyrosine and increase the relative levels of non-phosphorylated β-dystroglycan in sapje zebrafish. Furthermore, dasatinib treatment resulted in the improved physical appearance of the sapje zebrafish musculature and increased swimming ability as measured by both duration and distance of swimming dasatinib treated fish compared to control animals. These data suggest great promise for pharmacological agents that prevent the phosphorylation of β-dystroglycan on tyrosine and subsequent steps in the degradation pathway as therapeutic targets for the treatment of Duchenne muscular dystrophy.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping