Key mechanism identified in brain tumor growth
Discovery offers hope for more effective treatments of deadly glioblastomas
A gene known as OSMR plays a key role in driving the growth of glioblastoma tumors, according to a new study led by a 91社区 researcher and published in the journal Nature Neuroscience.
Glioblastoma is the most aggressive type of brain tumor in adults. Unfortunately, there are no effective treatments for the disease. On average, patients succumb just 16 months after diagnosis.
鈥淭o develop better treatments, we need to gain a better understanding of what is really going on inside these tumors,鈥� says lead author Arezu Jahani-Asl, Assistant Professor of Medicine at 91社区 and neuroscientist at the Jewish General Hospital鈥檚 Lady Davis Institute for Medical Research in Montreal.
A missing piece of the puzzle
Researchers had known for some time that a mutant variation of another gene, known as EGFRvIII, produces a major tumor-forming protein in glioblastoma. But treatments aimed at disabling EGFRvIII in these patients have been disappointingly ineffective.
Some piece of the molecular puzzle must have been missing.
So Jahani-Asl went hunting for it in tissue samples from glioblastoma patients as she was pursuing a postdoctoral fellowship in the laboratories of Azad Bonni at Harvard Medical School and Washington University School of Medicine and Michael Rudnicki at The Ottawa Hospital and the University of Ottawa. The researchers discovered that the OSMR gene was very active in glioblastoma cells. What鈥檚 more, by using existing cancer genetic and clinical databases they found that the more active this gene was, the shorter the patient鈥檚 life span.
The research team then studied human brain tumor stem cells taken from glioblastoma patients. These cells are normally able to proliferate and form new tumors when injected into laboratory mice. To the researchers鈥� surprise, however, they found that when they knock down the gene for OSMR in glioblastoma cells and inject these cells in mice聽they lose their ability to form tumors. 鈥淚t means that this protein is a key piece of the puzzle,鈥� says Rudnicki, senior co-corresponding author of the study.
The researchers concluded that these two genes, OSMR and EGFRvIII, conspire to promote tumor growth by making what鈥檚 known as a 鈥渇eed forward鈥� mechanism: when OSMR produces its protein, that signals EGFRvIII to rev up and produce its tumor-forming protein.
So disable OSMR and you disable EGFRvIII.
Potential target for treatments
鈥淭he discovery has important clinical implications,鈥� says Bonni, senior co-corresponding author. 鈥淚t provides a new therapeutic avenue for treating this devastating disease, though developing any effective therapy targeting human patients could be years of work.鈥�
Jahani-Asl is now developing antibodies and small molecules designed to inhibit the OSMR protein or its interaction with EGFRvIII 鈥� a step toward the ultimate goal of finding ways to treat these tumors. 鈥淚f we find that they can reverse tumor formation in rodent models,鈥� she says, 鈥渨e will be equipped to adapt those techniques for testing in patients.鈥�
Funding for the research was provided by the U.S. National Institutes of Health, the Canadian Institutes for Health Research, the Mathers Foundation, and the Canada Research Chairs program.
鈥淐ontrol of glioblastoma tumorigenesis by feed-forward cytokine signaling,鈥� Arezu Jahani-Asl et al, Nature Neuroscience, published online April 25, 2016.
DOI: 10.1038/nn.4295
滨惭础骋贰:听Human brain tumor stem cells expressing OSMR (green). CREDIT: Takrima Haque, laboratory of Arezu Jahani-Asl
