DNA Methylation Profiling As a Model for Discovery and Precision Diagnostics in Neuro-oncology
Overview
Authors
Affiliations
Recent years have witnessed a shift to more objective and biologically-driven methods for central nervous system (CNS) tumor classification. The 2016 world health organization (WHO) classification update ("blue book") introduced molecular diagnostic criteria into the definitions of specific entities as a response to the plethora of evidence that key molecular alterations define distinct tumor types and are clinically meaningful. While in the past such diagnostic alterations included specific mutations, copy number changes, or gene fusions, the emergence of DNA methylation arrays in recent years has similarly resulted in improved diagnostic precision, increased reliability, and has provided an effective framework for the discovery of new tumor types. In many instances, there is an intimate relationship between these mutations/fusions and DNA methylation signatures. The adoption of methylation data into neuro-oncology nosology has been greatly aided by the availability of technology compatible with clinical diagnostics, along with the development of a freely accessible machine learning-based classifier. In this review, we highlight the utility of DNA methylation profiling in CNS tumor classification with a focus on recently described novel and rare tumor types, as well as its contribution to refining existing types.
Diagnostic impact of DNA methylation classification in adult and pediatric CNS tumors.
Lebrun L, Gilis N, Dausort M, Gillard C, Rusu S, Slimani K Sci Rep. 2025; 15(1):2857.
PMID: 39843975 PMC: 11754448. DOI: 10.1038/s41598-025-87079-4.
Pediatric neuro-oncology: Highlights of the last quarter-century.
Power P, Straehla J, Fangusaro J, Bandopadhayay P, Manoharan N Neoplasia. 2024; 59:101098.
PMID: 39637686 PMC: 11664148. DOI: 10.1016/j.neo.2024.101098.
Specifics of spinal neuropathology in the molecular age.
Kresbach C, Hack K, Ricklefs F, Schuller U Neurooncol Adv. 2024; 6(Suppl 3):iii3-iii12.
PMID: 39430396 PMC: 11485660. DOI: 10.1093/noajnl/vdad127.
Wang L, Xu S, Chen R, Ding Y, Liu M, Hou C Front Endocrinol (Lausanne). 2024; 15:1429514.
PMID: 39247918 PMC: 11377254. DOI: 10.3389/fendo.2024.1429514.
RNA splicing as a biomarker and phenotypic driver of meningioma DNA-methylation groups.
Leclair N, Choudury A, Chen W, Magill S, McCortney K, Horbinski C Neuro Oncol. 2024; 26(12):2222-2236.
PMID: 39093629 PMC: 11630566. DOI: 10.1093/neuonc/noae150.