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Tumours are made up of a variety of cells, both cancerous and non-cancerous. The unique complexity of the cells within brain tumours has become a signature of the disease, making therapy extremely challenging. While scientists have long known about the many cells that make up a brain tumour, the way these tumours grow has relied on the assumption that the cells are static, immobile, and largely unchanging.
However, according to research published in the journal 'Nature Communications', researchers from the University of Michigan's Department of Neurosurgery and the Rogel Cancer Center revealed that these aggressive tumours contain highly active cells that migrate throughout tissue in complex patterns. Furthermore, accumulations of these elongated, spindle-like cells present throughout the tumour, known as 'oncostreams,' serve as the foundation for malignant cell behaviour, determining how tumours develop and infiltrate normal tissue. Pedro Lowenstein, M.D., Ph.D., Richard C. Schneider Collegiate Professor of Neurosurgery and lead author of this study in Nature Communications, says this organized growth is what makes brain tumors so relentless. "Brain tumors are highly lethal, with less than 5% of patients living beyond five years," he said. "Unfortunately, reoccurrence is what eventually kills patients. They receive surgery for their initial tumor, but the tumor always comes back within 12 to 18 months," he said. Lowenstein and his team, including Maria Castro, Ph.D., also found that overexpression of Collagen 1, a protein produced by tumor cells, is essential to the growth and function of these structures. "When we eliminated Collagen 1 production from tumor cells, the animal models with brain tumors lived much longer. This step removes oncostreams from tumors and reduces tumor aggressive behavior because the tumors need Collagen 1 to move in the specific way we discovered," said Lowenstein. Lowenstein says this structure is likely present in other types of cancer, too. "Once people recognize that there are dynamic areas of the tumor, and that they're related to tumor growth, eventual invasion and death, people will likely locate oncostreams in other tumor models," he said. To detect this previously unknown presence of oncostreams, the team collaborated with Todd Hollon, M.D., assistant professor in the Michigan Medicine Department of Neurological Surgery, and Sebastien Motsch, Ph.D., associate professor of mathematics at Arizona State University, to implement artificial intelligence methods to identify the structures in tissue. "Essentially, we showed images to a computer and the computer eventually learns to recognize oncostreams," Lowenstein explained. Dismantling oncostreams through the removal of Collagen 1 could represent a novel therapeutic target to treat lethal brain tumors. "This research proves the crucial importance of continuing to investigate the complicated extracellular matrix," notes Andrea Comba, Ph.D., research investigator and first author of the study. "Based on this discovery, we propose targeting tumor collagen to disrupt oncostreams, and as novel therapy for the treatment of brain glioma," she said. (ANI)
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