Update on pharmacogenetics in cancer chemotherapy

Eur J Cancer. 2002 Mar;38(5):639-44. doi: 10.1016/s0959-8049(01)00434-8.

Abstract

This review describes how genetic differences among patients may change the therapeutic outcome in cancer chemotherapy. Severe toxicity in genetically predisposed patients is predominantly associated with mutations in drug metabolism enzyme genes, and an update on genetic intolerance to 6-mercaptopurine, 5-fluorouracil, and irinotecan is provided. Moreover, recent findings pointed out that the methylenetetrahydrofolate reductase (MTHFR) C677T mutation might change patient susceptibility to the toxic effects of the cyclophosphamide, methotrexate, 5-fluorouracil (CMF) regimen and raltitrexed. Finally, it is emerging that not only toxicity, but also response to chemotherapy could be influenced by pharmacogenetic determinants, and the clinical relevance of polymorphisms in thymidylate synthase (TS) and glutathione-S-transferase (GST) genes is discussed.

Publication types

  • Research Support, U.S. Gov't, P.H.S.
  • Review

MeSH terms

  • Antineoplastic Agents / adverse effects
  • Antineoplastic Agents / pharmacokinetics
  • Antineoplastic Agents / therapeutic use*
  • Glutathione Transferase / genetics
  • Humans
  • Mutation
  • Neoplasms / drug therapy*
  • Neoplasms / genetics*
  • Pharmacogenetics
  • Thymidylate Synthase / genetics

Substances

  • Antineoplastic Agents
  • Thymidylate Synthase
  • Glutathione Transferase