Practical implementation of DNA methylation and copy-number-based CNS tumor diagnostics: the Heidelberg experience

Acta Neuropathol. 2018 Aug;136(2):181-210. doi: 10.1007/s00401-018-1879-y. Epub 2018 Jul 2.

Abstract

Recently, we described a machine learning approach for classification of central nervous system tumors based on the analysis of genome-wide DNA methylation patterns [6]. Here, we report on DNA methylation-based central nervous system (CNS) tumor diagnostics conducted in our institution between the years 2015 and 2018. In this period, more than 1000 tumors from the neurosurgical departments in Heidelberg and Mannheim and more than 1000 tumors referred from external institutions were subjected to DNA methylation analysis for diagnostic purposes. We describe our current approach to the integrated diagnosis of CNS tumors with a focus on constellations with conflicts between morphological and molecular genetic findings. We further describe the benefit of integrating DNA copy-number alterations into diagnostic considerations and provide a catalog of copy-number changes for individual DNA methylation classes. We also point to several pitfalls accompanying the diagnostic implementation of DNA methylation profiling and give practical suggestions for recurring diagnostic scenarios.

Keywords: Copy-number variation; DNA methylation; EPIC array; Tumor classification.

MeSH terms

  • Central Nervous System Neoplasms / classification*
  • Central Nervous System Neoplasms / genetics*
  • DNA Copy Number Variations / genetics*
  • DNA Methylation / genetics*
  • DNA Modification Methylases / genetics
  • DNA Repair Enzymes / genetics
  • Female
  • Humans
  • Isocitrate Dehydrogenase / genetics
  • Male
  • Neoplasm Proteins / genetics*
  • Receptor Protein-Tyrosine Kinases / genetics
  • Retrospective Studies
  • Tumor Suppressor Proteins / genetics

Substances

  • Neoplasm Proteins
  • Tumor Suppressor Proteins
  • Isocitrate Dehydrogenase
  • IDH1 protein, human
  • DNA Modification Methylases
  • MGMT protein, human
  • Receptor Protein-Tyrosine Kinases
  • DNA Repair Enzymes