GPx3 promoter hypermethylation is a frequent event in human cancer and is associated with tumorigenesis and chemotherapy response

Cancer Lett. 2011 Oct 1;309(1):37-45. doi: 10.1016/j.canlet.2011.05.013.

Abstract

Glutathione peroxidase 3 (GPx3), a plasma antioxidant enzyme, maintains genomic integrity by inactivating reactive oxygen species (ROS), known DNA-damaging agents and mediators of cancer chemotherapy response. In this study, we demonstrate that loss of GPx3 expression by promoter hypermethylation is frequently observed in a wide spectrum of human malignancies. Furthermore, GPx3 methylation correlates with head and neck cancer (HNC) chemoresistance and may serve as a potential prognostic indicator for HNC patients treated with cisplatin-based chemotherapy. Our findings support the hypothesis that defects in the antioxidant system may contribute to tumorigenesis of a wide spectrum of human malignancies. GPx3 methylation may have implications in chemotherapy response and clinical outcome of HNC patients.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antineoplastic Agents / therapeutic use
  • Cell Line, Tumor
  • DNA Methylation*
  • Down-Regulation
  • Female
  • Gene Expression Regulation, Enzymologic
  • Gene Expression Regulation, Neoplastic
  • Glutathione Peroxidase* / genetics
  • Glutathione Peroxidase* / metabolism
  • Head and Neck Neoplasms / drug therapy
  • Head and Neck Neoplasms / enzymology
  • Head and Neck Neoplasms / genetics
  • Humans
  • Male
  • Neoplasms / drug therapy
  • Neoplasms / enzymology*
  • Neoplasms / etiology
  • Neoplasms / genetics
  • Polymerase Chain Reaction
  • Prognosis
  • Treatment Outcome

Substances

  • Antineoplastic Agents
  • GPX3 protein, human
  • Glutathione Peroxidase