High-throughput detection of glutathione s-transferase polymorphic alleles in a pediatric cancer population

Cancer Epidemiol Biomarkers Prev. 2004 Feb;13(2):304-13. doi: 10.1158/1055-9965.epi-03-0178.

Abstract

Polymorphisms of glutathione S-transferase (GST) enzymes have been correlated with altered risk of several cancers, as well as altered response and toxicity from cancer chemotherapy. We report a low cost, highly reproducible and specific PCR-based high-throughput assay for genotyping different GSTs designed for use in large clinical trials. In comparison to an alternative genotyping method (single nucleotide extension), the sensitivity and specificity of the high throughput assay was shown to be 92 and 97%, respectively, depending on the source of genomic DNA. Using the high-throughput assay, we demonstrate by multivariate analysis an increased risk of acute lymphoblastic leukemia, glial brain tumors, and osteosarcoma for patients carrying nonnull alleles of GSTM1 and/or GSTT1.

Publication types

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

MeSH terms

  • Antineoplastic Agents / adverse effects
  • Antineoplastic Agents / metabolism
  • Child
  • Child, Preschool
  • Cost Control
  • DNA Primers
  • DNA, Neoplasm / genetics*
  • Female
  • Genotype
  • Glutathione Transferase / genetics*
  • Glutathione Transferase / pharmacology
  • Humans
  • Male
  • Neoplasms / drug therapy
  • Neoplasms / genetics
  • Polymerase Chain Reaction / economics
  • Polymerase Chain Reaction / methods*
  • Polymorphism, Genetic*
  • Reproducibility of Results
  • Sensitivity and Specificity

Substances

  • Antineoplastic Agents
  • DNA Primers
  • DNA, Neoplasm
  • Glutathione Transferase