The breakthrough, co-funded by the charity Brain Tumor Research, is significant because, if further research is conclusive, the anti-retroviral drugs could be prescribed for patients diagnosed with meningioma and acoustic neuroma brain tumors (also known as schwannoma).
More effective approaches are urgently needed as there are very few treatment options for these tumor types which frequently return following surgery and radiotherapy.
Meningioma is the most common form of primary brain tumor. Mostly low-grade, it can become cancerous over time, and develops from cells located in the meninges which protect the brain and spinal cord. Acoustic neuroma is a different type of low-grade, or non-cancerous brain tumor, which develops in nerve-protecting cells called Schwann cells. Both tumors may occur spontaneously, usually in adulthood, or in the hereditary disease Neurofibromatosis type 2 (NF2) in childhood/early adolescence.
Researchers at the Brain Tumor Research Centre at the University of Plymouth have shown previously that a tumor suppressor, named Merlin, contributes to the development of meningioma, acoustic neuroma and ependymoma tumors. It can also contribute to neurofibromatosis type 2 (NF2). Tumor suppressor genes play important roles in normal cells by controlling division or repairing errors in DNA. However, when tumor suppressors do not work properly or are absent, cells can grow out of control, leading to cancer.
In this latest study Dr Sylwia Ammoun, Senior Research Fellow, and her collaborator, Dr Robert Belshaw investigated the role that specific sections of our DNA play in tumor development. Named ‘endogenous retrovirus HERV-K’, these sections of DNA are relics of ancient infections that affected our primate ancestors, which have become stable elements of human DNA.