Tumor-specific methylations in circulating cell-free DNA as clinically applicable markers with potential to substitute mutational analyses

Expert Rev Mol Diagn. 2018 Dec;18(12):1011-1019. doi: 10.1080/14737159.2018.1545576. Epub 2018 Nov 13.

Abstract

Introduction: Analysis of circulating tumor DNA is a promising approach to guide the treatment of cancer patients but despite large efforts it has not been broadly applied in the clinic. Technical obstacles and lack of standardization have hampered the process and it has proved challenging to make highly sensitive analyses available for all patients. Research has focused on the use of somatic mutations but because of large mutational diversity among patients the setup becomes unmanageable for daily routine use. Areas covered: Methylations are key events in cancer development and can be used as markers for the presence of circulating tumor DNA similar to how mutations have been used. This review focuses on analytical aspects and possible clinical applications of methylated ctDNA in plasma from cancer patients. Expert commentary: Technical and clinical challenges of mutation and methylation analyses are similar. However, the possibility to analyze a limited number of methylations present in all tumors of a certain type allows for proper validation and standardization of the analyses. Tumor-specific methylation analyses could supplement or substitute mutation analyses for certain clinical applications and assist the progress of the clinical use of circulating tumor DNA.

Keywords: Circulating tumor DNA; DNA methylation; biomarker; mutation analyses; plasma; tumor monitoring.

Publication types

  • Review

MeSH terms

  • Biomarkers, Tumor / blood*
  • Cell-Free Nucleic Acids / blood*
  • Circulating Tumor DNA / blood*
  • Circulating Tumor DNA / genetics
  • DNA Mutational Analysis
  • DNA, Neoplasm / blood
  • Humans
  • Neoplasms / blood*
  • Neoplasms / genetics

Substances

  • Biomarkers, Tumor
  • Cell-Free Nucleic Acids
  • Circulating Tumor DNA
  • DNA, Neoplasm