Variant of the CHEK2 gene as a prognostic marker in glioblastoma multiforme

Neurosurgery. 2006 Nov;59(5):1078-85; discussion 1085. doi: 10.1227/01.NEU.0000245590.08463.5B.

Abstract

Objective: Germline mutations of the CHEK2 tumor suppressor gene have been found in families with the Li-Fraumeni syndrome (LFS). Patients with LFS experience a variety of cancers, including malignant astrocytomas. We investigated a potential role for a CHEK2 gene polymorphism in glioblastomas.

Methods: A genetic polymorphism of the CHEK2 gene (CHEK2 SNP rs2017309 A/T) was genotyped in a series of glioblastoma patients (n = 213) and population controls (n = 192). Subsets of tumors were analyzed for loss of heterozygosity 22q(n = 66), loss of heterozygosity CHEK2 (n = 53), CHEK2 expression (n = 21), and CHEK2 coding sequence alterations (n = 18). CHEK2 SNP rs2017309 genotyping findings and traditional clinicopathological parameters were correlated with the patients' prognoses.

Results: No association between the CHEK2 SNP and glioblastoma formation was observed. No CHEK2 coding sequence aberrations or tumors completely lacking CHEK2 protein were identified. However, the presence of the CHEK2 rs2017309 A allele was significantly associated with an adverse prognosis (P = 0.034), particularly among patients undergoing postoperative chemotherapy and radiotherapy (n = 28, median survival 10.5 versus 15.5 mo, P = 0.008). We could confirm the patients' age, Karnofsky Performance Scale score, and postoperative radiotherapy and chemotherapy (all P < 0.0001, log-rank test) as decisive prognostic factors.

Conclusion: Our data suggest that a CHEK2 gene polymorphism might correlate with the prognosis of glioblastoma patients. These findings may point to an as yet unrecognized role for the CHEK2 gene in glioblastomas.

Publication types

  • Controlled Clinical Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biomarkers / blood
  • Biomarkers, Tumor / blood
  • Biomarkers, Tumor / genetics
  • Brain Neoplasms / blood
  • Brain Neoplasms / genetics*
  • Brain Neoplasms / mortality*
  • Checkpoint Kinase 2
  • Female
  • Genetic Predisposition to Disease / epidemiology
  • Genetic Predisposition to Disease / genetics
  • Genetic Testing / methods
  • Genetic Variation / genetics
  • Glioblastoma / blood
  • Glioblastoma / genetics*
  • Glioblastoma / mortality*
  • Humans
  • Male
  • Neoplasm Proteins / blood
  • Neoplasm Proteins / genetics
  • Polymorphism, Single Nucleotide / genetics
  • Prevalence
  • Prognosis
  • Protein Serine-Threonine Kinases / blood*
  • Protein Serine-Threonine Kinases / genetics*
  • Risk Assessment / methods*
  • Risk Factors
  • Statistics as Topic
  • Survival Analysis
  • Survival Rate

Substances

  • Biomarkers
  • Biomarkers, Tumor
  • Neoplasm Proteins
  • Checkpoint Kinase 2
  • CHEK2 protein, human
  • Protein Serine-Threonine Kinases