Whole-genome mRNA expression profiling identifies functional and prognostic signatures in patients with mesenchymal glioblastoma multiforme

CNS Neurosci Ther. 2013 Sep;19(9):714-20. doi: 10.1111/cns.12118. Epub 2013 May 11.

Abstract

Background: The Cancer Genome Atlas (TCGA) has divided patients with glioblastoma multiforme (GBM) into four subtypes based on mRNA expression microarray. The mesenchymal subtype, with a larger proportion, is considered a more lethal one. Clinical outcome prediction is required to better guide more personalized treatment for these patients.

Aims: The objective of this study was to identify a mRNA expression signature to improve outcome prediction for patients with mesenchymal GBM.

Results: For signature identification and validation, we downloaded mRNA expression microarray data from TCGA as training set and data from Rembrandt and GSE16011 as validation set. Cox regression and risk-score analysis were used to develop the 4 signatures, which were function and prognosis associated as revealed by Gene Ontology (GO) analysis and Gene Set Variation Analysis (GSVA). Patients who had high-risk scores according to the signatures had poor overall survival compared with patients who had low-risk scores.

Conclusions: The signatures were identified as risk predictors that patients who had a high-risk score tended to have unfavorable outcome, demonstrating their potential for personalizing cancer management.

Keywords: Biomarker; Glioblastoma; Mesenchymal; Prognosis; Risk score.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Brain Neoplasms / genetics*
  • Brain Neoplasms / mortality
  • Gene Expression Profiling*
  • Genome, Human
  • Glioblastoma / genetics*
  • Glioblastoma / mortality
  • Humans
  • Prognosis
  • Proportional Hazards Models
  • RNA, Messenger / analysis*

Substances

  • RNA, Messenger