Posted by Friends of FSH Research on Feb 1, 2021
Update by Dr. Saad
See grant Development of novel DUX4-targeted miR-675- based therapies for FSHD
Facioscapulohumeral dystrophy (FSHD) is a genetic muscle disease caused by the unusual presence of DUX4 in skeletal muscles. As a result, skeletal muscles become damaged and weak. In our proposed project, we developed two therapeutic strategies for FSHD. These strategies rely on the power of natural small molecules called “microRNAs” that are normally found in many human tissues, among them skeletal muscles. The natural function of these microRNAs is to decrease the levels of proteins in a cell. Each microRNA can specifically decrease the level of one or more proteins. In fact, a microRNA becomes more efficient in decreasing the levels of its target protein when it becomes more abundant in the cell. Accordingly, in our 1st therapeutic strategy, we used adeno-associated virus (AAV)-based gene therapy to deliver our microRNA into mice skeletal muscles expressing DUX4. Our results are very promising as our natural microRNA was able to efficiently prevent the production of DUX4 and thus prevented DUX4 from damaging muscle. In our second therapeutic strategy, we used pharmaceutical drugs to increase the abundance of our natural microRNA in human skeletal muscle cells. This strategy showed very promising results as these drugs were able to efficiently reduce DUX4 and DUX4-associated biomarkers. Our ongoing work will now focus on testing the efficiency of our natural microRNA to enhance muscle regeneration in mice and to test this microRNA in our FSHD mouse model. This project is very promising as it would lay the ground to bring to the clinic a therapeutic natural microRNA and pharmaceutical drugs that increase its level. As a result, these therapies will eliminate DUX4 from skeletal muscles, stop muscle degradation and possibly enhance muscle regeneration, allowing not just the recovery of skeletal muscles but also allowing them to become stronger.