Technology Listings


Compounds for Suppressing Fragile X Premutation rCGG Repreat-Mediated Toxicity

Application

Compounds for the treatment of Fragile X-associated tremor/ataxia syndrome.

Key Benefits
  • 11 known, FDA approved drugs identified that reduced rCGG-mediated lethality to a certain degree.
  • 3 of these drugs also rescued locomotion deficits.
Technical Summary

Fragile X syndrome (FXS) is the most common inheritable form of cognitive disability affecting nearly 1 in 4000 males and 1 in 6000 females. FXS usually results from the expansion of the CGG trinucleotide repeat in the 5' untranslated region (5' UTR) of the fragile X mental retardation 1 (FMR1) gene. Within the last decade, Fragile X-associated tremor/ataxia syndrome (FXTAS), a late age of onset neurodegenerative disorder, has been recognized among many FXS carriers in or beyond the fifth decade of life. Interestingly, 1 in every 800 males is a carrier and considered at high risk for developing FXTAS.

FXTAS is uncoupled from the neurodevelopmental disorder, FXS, and its most common clinical feature is a progressive action tremor with ataxia. More advanced or severe cases can show a progressive cognitive decline that ranges from memory deficits to dementia. Patients may also experience increased anxiety, mood liability, depression, muscle weakness, and numbness and/or pain in the lower extremities.

Dr. Peng Jin and his colleagues developed a dual assay screen - viability and behavioral - in the drosophila model of FXTAS and identified three compounds that rescued the FXTAS phenotype. Two of the compounds are phospholipase A2 (PLA2) inhibitors, which the researchers believe, based on the biological mechanisms of PLA2, can suppress rCGG-mediated neurodegeneration.

Developmental Stage

3 FDA approved drugs have been identified that can rescue the FXTAS phenotype in a drosophila model; clinical studies are planned.

Patent Information
App Type Country Serial No. Patent No. File Date Issued Date Expire Date
Utility(parent) United States 13/457,718 8,618,077 4/27/2012 12/31/2013 4/27/2032
Tech ID: 09144
Published: 2/24/2011
Category
Therapeutics

Contact
Cliff Michaels
Assistant Director
Emory University
404-727-3890
ccmicha@emory.edu

Inventor(s)
Peng Jin
Abrar Qurashi

Keywords
Genetic Disorders
Neuroscience/Pain
Rare/Orphan Diseases
Repurposed Drug