Glioblastoma is the most common and most aggressive primary brain tumor. Despite maximum treatment, patients only have a median survival time of 15 months, because of the tumor's resistance to current therapeutic approaches. Thus far, methylation of the O 6-methylguanine-DNA methyltransferase (MGMT) promoter has been the only confirmed molecular predictive factor in glioblastoma. Novel "genome-wide" techniques have identified additional important molecular alterations as mutations in isocitrate dehydrogenase 1 (IDH1) and its prognostic importance. This review summarizes findings and techniques of genetic, epigenetic, transcriptional, and proteomic studies of glioblastoma. It provides the clinician with an up-to-date overview of current identified molecular alterations that should ultimately lead to new therapeutic targets and more individualized treatment approaches in glioblastoma.

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doi.org/10.1007/s11060-011-0793-0, hdl.handle.net/1765/73666
Journal of Neuro-Oncology
Department of Neurosurgery

Bleeker, F., Molenaar, R., & Leenstra, S. (2012). Recent advances in the molecular understanding of glioblastoma. Journal of Neuro-Oncology (Vol. 108, pp. 11–27). doi:10.1007/s11060-011-0793-0