Somatic POLE mutations cause an ultramutated giant cell high-grade glioma subtype with better prognosis


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Erson-Omay E. Z., ÇAĞLAYAN A. O., Schultz N., Weinhold N., Omay S. B., ÖZDUMAN K., ...More

NEURO-ONCOLOGY, vol.17, no.10, pp.1356-1364, 2015 (SCI-Expanded) identifier identifier

  • Publication Type: Article / Article
  • Volume: 17 Issue: 10
  • Publication Date: 2015
  • Doi Number: 10.1093/neuonc/nov027
  • Journal Name: NEURO-ONCOLOGY
  • Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Page Numbers: pp.1356-1364
  • Keywords: better prognosis, glioblastoma, polymerase epsilon, germline MSH6 mutation, ultramutated tumor, DNA-POLYMERASE EPSILON, GENOMIC CHARACTERIZATION, GLIOBLASTOMA-MULTIFORME, ENDOMETRIOID CARCINOMA, GERMLINE MUTATIONS, MALIGNANT GLIOMAS, CANCER GENOMICS, MSH6 MUTATIONS, GENES, LANDSCAPE
  • Dokuz Eylül University Affiliated: No

Abstract

Background. Malignant high-grade gliomas (HGGs), including the most aggressive form, glioblastoma multiforme, show significant clinical and genomic heterogeneity. Despite recent advances, the overall survival of HGGs and their response to treatment remain poor. In order to gain further insight into disease pathophysiology by correlating genomic landscape with clinical behavior, thereby identifying distinct HGG molecular subgroups associated with improved prognosis, we performed a comprehensive genomic analysis.