UCLA scientists have developed a potentially promising new combination therapy for glioblastoma, the most common and deadliest form of brain cancer. Glioblastoma, also known as grade IV glioma, is an aggressive primary brain tumor in humans. Approximately 23,000 people in the U.S. are diagnosed with glioblastoma every year. Patients usually receive surgery, chemotherapy and radiation, but these treatments are not very effective as an estimated 50 percent of GBM patients die within one year, and 90 percent die within three years. A study led by Dr. Robert Prins and Dr. Linda Liau, both members of the UCLA Jonsson Comprehensive Cancer Center, looked at the impact of a combined treatment using a chemotherapy drug called decitabine and genetically modified immune cells. It is a continuation of previous research, published in 2011, that focused on the effect of decitabine on glioblastoma human cell cultures. In the new research, Prins and Liau used a technique called engineered adoptive T cell transfer, which involves extracting and growing immune cells outside of the body, then reprogramming them with the gene for a T cell receptor targeting New York esophageal squamous carcinoma, or NY-ESO-1. They are then injected back into mice with glioblastoma tumors to produce an immune response that targets the brain cancer. Glioblastoma cells do not naturally produce NY-ESO-1, so the researchers administered decitabine prior to injecting the reprogrammed T cells in order to cause the tumor cells to express the NY-ESO-1 target. “The lymphocytes will seek out and find the glioblastoma cells in the brain,” said Prins, UCLA associate professor in the departments of neurosurgery and molecular and medical pharmacology. “They can cross different fiber tracts in the brain to reach tumor cells that have migrated away from the main tumor mass. These factors are important in the treatment of invasive tumors, such as glioblastoma. While surgery to remove the main tumor mass can be done, it is not possible to then locate the tumor cells that get away and this ultimately leads to a nearly universal tumor regrowth.” This new method was about 50 percent effective at curing glioblastoma in the study. According to the researchers the implications of this study are significant since it is difficult to predict who will develop PTSD following traumatic events. Image is for illustrative purposes only. Credit: Sbrandner. “Brain cancer cells are very good at evading the host immune system, because they do not express specific targets that can be recognized by immune cells,” said Liau, UCLA professor and vice chair of neurosurgery. “By treating glioblastoma cells with decitabine, we found that we can unmask targets on the tumor cell that can be recognized by killer T cells. Once these targets are uncovered, we can then administer T cells that are genetically programmed to attack tumor cells with the new targets.” The next stage of Prins’ and Liau’s research will verify these findings in other brain tumor models. [divider]About this brain cancer research[/divider] Funding: Funding for the study was provided by the Jonsson Cancer Center Foundation at UCLA and the AANS Neurosurgery Research Education Fund. Source: Reggie Kumar – UCLA Image Source: The image is credited to Sbrandner and is licensed GFDL Original Research: Abstract for “Efficacy of systemic adoptive transfer immunotherapy targeting NY-ESO-1 for glioblastoma” by Richard G. Everson, Joseph P. Antonios, Dominique N. Lisiero, Horacio Soto, Rudi Scharnweber, Matthew C. Garrett, William H. Yong, Ning Li, Gang Li, Carol A. Kruse, Linda M. Liau, and Robert M. Prins in Neuro-Oncology. Published online September 1 2015 doi:10.1093/neuonc/nov153 AbstractSee alsoFeaturedNeuroscience·May 13, 2020Signs of fetal alcohol syndrome detected in womb Efficacy of systemic adoptive transfer immunotherapy targeting NY-ESO-1 for glioblastoma Background Immunotherapy is an ideal treatment modality to specifically target the diffusely infiltrative tumor cells of malignant gliomas while sparing the normal brain parenchyma. However, progress in the development of these therapies for glioblastoma has been slow due to the lack of immunogenic antigen targets that are expressed uniformly and selectively by gliomas. Methods We utilized human glioblastoma cell cultures to induce expression of New York–esophageal squamous cell carcinoma (NY-ESO-1) following in vitro treatment with the demethylating agent decitabine. We then investigated the phenotype of lymphocytes specific for NY-ESO-1 using flow cytometry analysis and cytotoxicity against cells treated with decitabine using the xCelligence real-time cytotoxicity assay. Finally, we examined the in vivo application of this immune therapy using an intracranially implanted xenograft model for in situ T cell trafficking, survival, and tissue studies. Results Our studies showed that treatment of intracranial glioma–bearing mice with decitabine reliably and consistently induced the expression of an immunogenic tumor-rejection antigen, NY-ESO-1, specifically in glioma cells and not in normal brain tissue. The upregulation of NY-ESO-1 by intracranial gliomas was associated with the migration of adoptively transferred NY-ESO-1–specific lymphocytes along white matter tracts to these tumors in the brain. Similarly, NY-ESO-1–specific adoptive T cell therapy demonstrated antitumor activity after decitabine treatment and conferred a highly significant survival benefit to mice bearing established intracranial human glioma xenografts. Transfer of NY-ESO-1–specific T cells systemically was superior to intracranial administration and resulted in significantly extended and long-term survival of animals. Conclusion These results reveal an innovative, clinically feasible strategy for the treatment of glioblastoma. “Efficacy of systemic adoptive transfer immunotherapy targeting NY-ESO-1 for glioblastoma” by Richard G. Everson, Joseph P. Antonios, Dominique N. Lisiero, Horacio Soto, Rudi Scharnweber, Matthew C. Garrett, William H. Yong, Ning Li, Gang Li, Carol A. Kruse, Linda M. Liau, and Robert M. Prins in Neuro-Oncology. 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