New research from the University of Adelaide looked at the relationship between brain tumours and a peptide associated with inflammation in the brain, called "substance P".
Substance P is commonly released throughout the body by the nervous system, and contributes to tissue swelling following injury. In the brain, levels of substance P greatly increase after traumatic brain injury and stroke.
"Researchers have known for some time that levels of substance P are also greatly increased in different tumour types around the body," said Dr Elizabeth Harford-Wright, a postdoctoral fellow in the University's Adelaide Centre for Neuroscience Research.
Harford-Wright found that levels of substance P were greatly increased in brain tumour tissue.
Knowing that substance P binds to a receptor called NK1, she used an antagonist drug called Emend to stop substance P binding to the receptor. Emend is already used in cancer clinics to help patients with chemotherapy-induced nausea.
"We were successful in blocking substance P from binding to the NK1 receptor, which resulted in a reduction in brain tumour growth - and it also caused cell death in the tumour cells," she said.
"This is a very exciting result, and it offers further opportunities to study possible brain tumour treatments over the coming years," she added.
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