4.6 Article

Spatial concordance of DNA methylation classification in diffuse glioma

Journal

NEURO-ONCOLOGY
Volume 23, Issue 12, Pages 2054-2065

Publisher

OXFORD UNIV PRESS INC
DOI: 10.1093/neuonc/noab134

Keywords

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Funding

  1. Cancer Center Amsterdam Support Grant [2012-2-05]
  2. Cancer Center Support Grant [P30CA034196]
  3. NIH/NCA [R01 CA190121, R01 CA237208]
  4. NIH/NINDS [R21 NS114873]
  5. Department of Defense [W81XWH1910246]
  6. Dutch Cancer Society Fellowship [OAA/H1/VU 2015-7502]
  7. Niels Stensen Fellowship
  8. JAX Scholar program
  9. National Cancer Institute [K99 CA226387]
  10. American Cancer Society Fellowship [130984-PF-17-141-01-DMC]
  11. NIHR Biomedical Research Centre at UCLH
  12. U.S. Department of Defense (DOD) [W81XWH1910246] Funding Source: U.S. Department of Defense (DOD)

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This study investigated intratumoral heterogeneity in diffuse gliomas using DNA methylation profiling, demonstrating the infiltrative nature of the tumors and the variability in tumor purity contributing to epigenetic spatial heterogeneity. The results suggest that DNA methylation subtypes in diffuse gliomas are relatively consistent, but some heterogeneity exists.
Background. Intratumoral heterogeneity is a hallmark of diffuse gliomas. DNA methylation profiling is an emerging approach in the clinical classification of brain tumors. The goal of this study is to investigate the effects of intratumoral heterogeneity on classification confidence. Methods. We used neuronavigation to acquire 133 image-guided and spatially separated stereotactic biopsy samples from 16 adult patients with a diffuse glioma (7 IDH-wildtype and 2 IDH-mutant glioblastoma, 6 diffuse astrocytoma, IDH-mutant and 1 oligodendroglioma, IDH-mutant and 1p19q codeleted), which we characterized using DNA methylation arrays. Samples were obtained from regions with and without abnormalities on contrastenhanced T1-weighted and fluid-attenuated inversion recovery MRI. Methylation profiles were analyzed to devise a 3-dimensional reconstruction of (epi)genetic heterogeneity. Tumor purity was assessed from clonal methylation sites. Results. Molecular aberrations indicated that tumor was found outside imaging abnormalities, underlining the infiltrative nature of this tumor and the limitations of current routine imaging modalities. We demonstrate that tumor purity is highly variable between samples and explains a substantial part of apparent epigenetic spatial heterogeneity. We observed that DNA methylation subtypes are often, but not always, conserved in space taking tumor purity and prediction accuracy into account. Conclusion. Our results underscore the infiltrative nature of diffuse gliomas and suggest that DNA methylation subtypes are relatively concordant in this tumor type, although some heterogeneity exists.

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