New link between fatal muscle wasting disease gene and cancer discovered

Now, a study, led by the University of Portsmouth, has found that the same gene has a role in oncology. A team of international researchers analysed a broad spectrum of malignant tissues, including from breast, ovarian, and gastrointestinal cancer patients.

The DMD gene expression was reduced in 80 per cent of these tumours. This low expression of dystrophins was associated with a more advanced stage of cancer and reduced survival across different tumours.

The paper, published in Cancers, calls for a re-evaluation of the current view that dystrophin expression is only important in muscles, and when found across numerous tissues is the result of an "illegitimate transcription."

Senior author, Professor Darek Gorecki from the School of Pharmacy and Biological Sciences at the University of Portsmouth, said: "The findings that the DMD gene has a role in tumours, expands the growing evidence of its significance beyond Duchenne muscular dystrophy.

"Further investigation is needed to better understand the role of DMD in malignancies and how it may be exploited in monitoring cancer progression and treatment."

Moreover, these findings build on the recent discovery that the disease begins much earlier than previously thought. In 2021, the team published results of modelling DMD to look at its development, from its initial trigger and first manifestation. They found evidence of abnormalities even before birth in the embryo.

Given the similarities between early embryo development and cancer formation, including invasive potential, changes in gene expression and other vital behaviours, the team decided to investigate the DMD gene across the spectrum of tumours, which led to this discovery.

Most boys with DMD are diagnosed between two and five years old by which time the damage to their bodies is already significant.

Professor Gorecki says these new findings should be taken into consideration as delay in identifying the condition may be preventing therapeutic interventions that could help slow, if not stop, disease progression.

"The job of DMD, the largest human gene known, is far more complex than previously believed," he explained.

"It must be better understood if we want to find effective treatments for pathologies caused by its mutations."