It’s only through the gifts we receive from fundraisers and donors that we’re able to invest in the most promising research advancements for Duchenne muscular dystrophy.
We’re proud to fund Dr. Toshifumi Yokota from the University of Alberta as his research to develop and test a new “cocktail” drug that may be beneficial for up to 45 percent of patients with Duchenne muscular dystrophy. Read the article below as shared by the University of Alberta on February 23, 2022, written by Gillian Rutherford:
Up to 45 percent of patients with the most common inherited neuromuscular disease could benefit from a new “cocktail” drug being developed at the University of Alberta, according to research published this week in the Proceedings of the National Academy of Sciences.
The drug could provide an effective and economical treatment to lessen symptoms for the six of every 100,000 people — usually boys — affected by Duchenne muscular dystrophy, a chronic muscle-wasting disease, according to lead researcher Toshifumi Yokota, professor of medical genetics in the Faculty of Medicine & Dentistry.
A Band-Aid for damaged genes
People with Duchenne muscular dystrophy, referred to as DMD, have various mutations in the body’s largest gene, dystrophin, which is a protein that cells need to stay intact. Dystrophin has 79 sections, or exons. If even one is missing, the body cannot produce dystrophin and the muscles degenerate.
There is no cure for DMD, but a new class of drugs called antisense oligonucleotides uses an approach called “exon skipping,” which acts like a Band-Aid over the missing exons so the body can skip over the damaged instructions and produce the protein needed to rebuild muscle tissue.
Now the U of A’s team of medical genetics researchers has combined six such DNA-like exon-skipping molecules to create a “cocktail” treatment that could help many more patients.
“Each of the previously developed exon-skipping molecules has been able to treat only around 10 per cent of DMD patients, because they have different mutations to their exons in different locations within the gene,” said Yokota.
“Our approach is to skip over 11 exons all at once, which would allow us to treat approximately 45 per cent of patients,” he explained.
Yokota is also the Friends of Garrett Cumming Research & Muscular Dystrophy Canada Endowed Research Chair.
Treatment could help improve heart muscle
The new cocktail also addresses another limitation of existing exon-skipping treatments, which is that they don’t penetrate the heart muscle, Yokota explained. While DMD patients often suffer from extreme skeletal body weakness, most die from heart failure.
“Our cocktail combines the antisense oligonucleotides with a new peptide, a short chain of amino acids, which allows the drug to penetrate the heart muscle,” he said.
Yokota’s team tested the new synthetic drug in patient-derived muscle tissue in test tubes and in mice. They found signs of dystrophin production, muscle building and improved heart function.
The next step will be to undertake toxicology testing and go through the regulatory steps to conduct clinical trials. Yokota and his colleagues recently launched a company that will help to commercialize the drug.
Yokota’s research was funded by the Canadian Institutes of Health Research, Jesse’s Journey, Heart and Stroke Foundation of Canada, the Stollery Children’s Hospital Foundation through the Women and Children’s Health Research Institute, the Friends of Garrett Cumming Research & Muscular Dystrophy Canada HM Toupin Neurological Science Research Chair Fund, and Alberta Innovates. He is a member of the Neuroscience and Mental Health Institute at the University of Alberta.