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      The somatic genomic landscape of glioblastoma.

      Cell
      Brain Neoplasms, genetics, metabolism, Female, Gene Expression Profiling, Gene Regulatory Networks, Glioblastoma, Humans, Male, Mutation, Proteome, analysis, Signal Transduction

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          Abstract

          We describe the landscape of somatic genomic alterations based on multidimensional and comprehensive characterization of more than 500 glioblastoma tumors (GBMs). We identify several novel mutated genes as well as complex rearrangements of signature receptors, including EGFR and PDGFRA. TERT promoter mutations are shown to correlate with elevated mRNA expression, supporting a role in telomerase reactivation. Correlative analyses confirm that the survival advantage of the proneural subtype is conferred by the G-CIMP phenotype, and MGMT DNA methylation may be a predictive biomarker for treatment response only in classical subtype GBM. Integrative analysis of genomic and proteomic profiles challenges the notion of therapeutic inhibition of a pathway as an alternative to inhibition of the target itself. These data will facilitate the discovery of therapeutic and diagnostic target candidates, the validation of research and clinical observations and the generation of unanticipated hypotheses that can advance our molecular understanding of this lethal cancer. Copyright © 2013 Elsevier Inc. All rights reserved.

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          Author and article information

          Journal
          24120142
          3910500
          10.1016/j.cell.2013.09.034

          Chemistry
          Brain Neoplasms,genetics,metabolism,Female,Gene Expression Profiling,Gene Regulatory Networks,Glioblastoma,Humans,Male,Mutation,Proteome,analysis,Signal Transduction

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