Glioblastma multiforme (GBM) is one of the most lethal primary brain tumors, with median survival for these patients only slightly over one year. Researchers at Boston University School of Medicine (BUSM), in collaboration with researchers from the City of Hope Hospital in Los Angeles, California, are looking toward novel therapeutic strategies for the treatment of GBM in the form of targeted therapies against a unique receptor, the interleukin-13 receptor alpha chain variant 2 (IL13Ralpha2). In a review article published in the October 2014 issue of Neuro-Oncology, the researchers discuss various targeted therapies against IL13Ralpha2 and early successes of clinical trials with these therapies in the treatment of GBM. The article also highlights the need for future trials to improve the efficacy and toxicity profiles of targeted therapies in this field. Targeted therapies, which are drugs that interfere with specific molecules involved in cancer growth, have been successfully used in the treatment of many cancers, including breast and blood cancers. Successful targets for therapies are specific to tumor cells and not found on normal cells. Selectively expressed on GBM and absent on surrounding brain tissue, the interleukin-13 receptor alpha chain variant 2 (IL13Ralpha2) was identified as a potential target for therapy for GBM two decades ago. IL13Ralpha2 also plays an important role in the growth of tumors. In normal physiologic conditions, IL-13 binds to the receptor IL13Ralpha1 and helps regulate immune responses. In cancer cells, IL-13 binds to the receptor IL13Ralpha2 and, through a series of steps, prevents cancer cells from undergoing normal cell death. Increased expression of IL13Ralpha2 promotes the progression of GBM. Since its discovery, IL13Ralpha2 has provided a target for therapies in GBM.
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