- Technology Readiness Level: 2
- Technology Validation: The Purdue researchers analyzed the effect of rapamycin and statins on the cellular and molecular phenotypes of Lowe Syndrome patient cells.
Abstract
Researchers at Purdue University have developed a therapeutic strategy for Lowe Syndrome (LS), a currently untreatable genetic disorder characterized by cognitive deficiencies, bilateral congenital cataracts and renal dysfunction that leads to the early death of those affected, often from kidney failure. The Purdue treatment method has the potential to reverse symptoms and offer patients a higher quality of life. The researchers designed this treatment regimen using rapamycin and statins, drugs approved by the FDA for other indications because of on those drugs' ability to target two molecular pathways implicated in LS. The drugs produced a phenotype similar to normal cells in a variety of tests on LS patient cells. This technology addresses the molecular basis of LS and promises to ameliorate symptoms. This strategy also has the potential to help those suffering from other genetic conditions in which the same cellular pathways are affected.
Website
https://prf.flintbox.com/technologies/BFE35E25A3FA4E42B0DE0CE5835E4935
Advantages
- Uses FDA Approved drugs with low risk of adverse effects
- Addresses the molecular basis of symptoms in Lowe Syndrome
- Therapeutic for Lowe Syndrome
- Strategy could be applied to other genetic conditions
Contact Information
Name: Joseph R Kasper
Email: JRKasper@prf.org
Phone: 765-588-3475