Canadian researchers uncover brain cells fueling glioblastoma growth

Scientists at McMaster University and the Hospital for Sick Children in Canada have discovered that oligodendrocytes, cells typically supporting nerve function, aid the growth of glioblastoma by sending signals to tumor cells. Blocking this communication slowed tumor progression in lab models. The findings suggest an existing HIV drug, Maraviroc, could be repurposed for treatment.

A team led by Sheila Singh at McMaster University and Jason Moffat at SickKids identified how oligodendrocytes contribute to glioblastoma, the most aggressive brain cancer with limited treatment options and short survival times. These cells, which normally protect nerve fibers, alter their role to support tumor expansion through a CCL5/CCR5 signaling pathway. In laboratory models, disrupting this interaction significantly reduced tumor growth, as detailed in a study published in Neuron this year. Kui Zhai and Nick Mikolajewicz served as co-first authors. Singh described glioblastoma as an ecosystem: “Glioblastoma isn't just a mass of cancer cells, it's an ecosystem. By decoding how these cells talk to each other, we've found a vulnerability that could be targeted with a drug that's already on the market.” The research highlights Maraviroc, an approved HIV medication targeting the CCR5 receptor, as a potential quick-repurposing candidate. Moffat noted, “This finding opens a promising path to explore whether blocking this pathway can speed progress toward new treatment options for patients.” The work builds on the pair's 2024 Nature Medicine paper on cancer exploiting brain development pathways and was supported by Canadian research grants.

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Microscopic view of enhanced natural killer cells attacking cancer cells due to a drug developed by McGill researchers.
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McGill researchers use reversible drug approach to boost natural killer cells against hard-to-treat cancers

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Researchers at McGill University report a drug-based method to temporarily enhance natural killer (NK) cells—an immune cell type—by inhibiting two proteins, improving the cells’ ability to attack several aggressive cancers in preclinical experiments.

Researchers report that a single injection of a modified herpes virus draws immune cells deep into glioblastoma tumors, leading to longer survival in a clinical trial. The therapy, tested on 41 patients with recurrent brain cancer, activates T cells that persist and attack cancer cells. Findings were published in Cell.

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Duke University researchers report that boosting the transfer of healthy mitochondria from support cells to sensory neurons reduced pain-like behaviors in mouse models of diabetic and chemotherapy-related peripheral neuropathy, an approach they say could address a root driver of nerve pain rather than simply blocking pain signals.

Researchers report that tanycytes—specialized cells lining the brain’s third ventricle—can help move tau protein from cerebrospinal fluid into the bloodstream, and that signs of tanycyte disruption in Alzheimer’s patient tissue may be associated with impaired tau removal. The findings, published March 5 in Cell Press Blue, are based on animal and cell experiments and analyses of human brain samples.

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