Genetic variants as potential predictive biomarkers in advanced colorectal cancer patients treated with oxaliplatin-based chemotherapy

J Cell Physiol. 2018 Mar;233(3):2193-2201. doi: 10.1002/jcp.25966. Epub 2017 May 23.

Abstract

Chemotherapy regimen containing oxaliplatin is often the first-line treatment for patient with advanced colorectal cancer. Oxaliplatin binds to DNA, leading to the formation of crosslinks and bulky adducts. Approximately 50% of patients with CRC benefit from treatment with oxaliplatin. It is possible that genetic variants in biological pathways involved in drug transportation, drug metabolism, DNA damage repair, and cell cycle modulation might affect the activity, or efficacy of oxaliplatin. Because oxaliplatin resistance may be related to these genetic variants and may therefore be an important reason for treatment failure, we have summarized the genetic variations that have been reported to be predictive markers of the response to oxaliplatin based therapy in patients with advanced CRC.

Keywords: colorectal cancer; oxaliplatin; predictive biomarkers; resistance.

Publication types

  • Review

MeSH terms

  • Antineoplastic Agents / therapeutic use*
  • Biological Transport / genetics
  • Cell Cycle / genetics
  • Colorectal Neoplasms / drug therapy*
  • Colorectal Neoplasms / genetics*
  • DNA Repair / genetics
  • Drug Resistance, Neoplasm / genetics*
  • Genetic Markers / genetics*
  • Humans
  • Inactivation, Metabolic / genetics
  • Organoplatinum Compounds / therapeutic use*
  • Oxaliplatin
  • Treatment Failure

Substances

  • Antineoplastic Agents
  • Genetic Markers
  • Organoplatinum Compounds
  • Oxaliplatin