Scientists at USC and UC San Diego have discovered a potential novel target for treating glioblastoma, the deadly brain cancer that took the life of Sen. John McCain and kills 15,000 Americans a year.

The target is the circadian "clock" found within the tumour stem cells, which governs how the tumour grows, multiplies and develops resistance to current treatments.

"We think this is opening the door to a whole new range of therapies," said Steve Kay, Provost Professor of neurology, biomedical engineering and biological sciences at the Keck School of Medicine of USC, who is working with Jeremy Rich, a neuro-oncologist at University of California, San Diego who specialises in malignant brain tumours. "It's a great example of collaboration and convergence."

Kay and Rich report their findings in Cancer Discovery.

Glioblastoma is rare but nearly always fatal, striking adults in their mid-60s.

Average survival is only 15 months.

That's because this type of cancer infiltrates surrounding brain tissue, making it impossible to eradicate, even after surgery, radiation and chemotherapy.

The tumour comes back, growing from stubborn cancer stem cells left behind.

Now scientists are focusing on a new potential vulnerability in those left-behind stem cells.

Kay is a pioneer in the study of circadian rhythms and the biochemical circadian clocks that regulate hundreds of activities, from sleep to digestion to body temperature.

Circadian clocks are comprised of specific protein molecules that interact in cells throughout the body, controlling how they grow, replicate and repair damage to their DNA.

When circadian timing is off in cells, it can cause disease.

Biological clocks that run fast or slow can result in disrupted or abnormal circadian rhythms, increasing the risk of developing cancer in some people.

When the team first examined the biological clocks of glioblastoma stem cells in the lab, Kay said the researchers found them "on steroids, on overdrive."

The cells' circadian clock was ramping up the cells' metabolism, making the cells stronger and more resistant to treatment and able to divide and multiply rapidly.

In collaboration with Synchronicity Pharma, a San Francisco-based biotechnology company, they used a small-molecule drug to target the proteins in the stem cells' circadian clocks to disrupt their activity.

The ramped-up metabolism abated, and the cells quickly died.

"This was a striking, amazing result nobody really predicted," Kay said. Small-molecule drugs can enter cells easily and in this case, cross the blood-brain barrier in mouse models of the disease.

Next, the researchers tested the small-molecule drug in an animal model of glioblastoma.

They found the animal models lived longer and the tumour shrank in size.

"This lays the groundwork for us to explore this as a novel therapy for glioblastoma," Kay said.

"In the near future, we're going to do more work with animal models of the tumour and compare our new drug with the current standard of care. Perhaps we can one day contribute towards meeting this terrible unmet medical need."

Source: University of Southern California