Back to Search
Start Over
DNA-methylome-assisted classification of patients with poor prognostic subventricular zone associated IDH-wildtype glioblastoma.
- Source :
-
Acta neuropathologica [Acta Neuropathol] 2022 Jul; Vol. 144 (1), pp. 129-142. Date of Electronic Publication: 2022 Jun 04. - Publication Year :
- 2022
-
Abstract
- Glioblastoma (GBM) derived from the "stem cell" rich subventricular zone (SVZ) may constitute a therapy-refractory subgroup of tumors associated with poor prognosis. Risk stratification for these cases is necessary but is curtailed by error prone imaging-based evaluation. Therefore, we aimed to establish a robust DNA methylome-based classification of SVZ GBM and subsequently decipher underlying molecular characteristics. MRI assessment of SVZ association was performed in a retrospective training set of IDH-wildtype GBM patients (n = 54) uniformly treated with postoperative chemoradiotherapy. DNA isolated from FFPE samples was subject to methylome and copy number variation (CNV) analysis using Illumina Platform and cnAnalysis450k package. Deep next-generation sequencing (NGS) of a panel of 130 GBM-related genes was conducted (Agilent SureSelect/Illumina). Methylome, transcriptome, CNV, MRI, and mutational profiles of SVZ GBM were further evaluated in a confirmatory cohort of 132 patients (TCGA/TCIA). A 15 CpG SVZ methylation signature (SVZM) was discovered based on clustering and random forest analysis. One third of CpG in the SVZM were associated with MAB21L2/LRBA. There was a 14.8% (n = 8) discordance between SVZM vs. MRI classification. Re-analysis of these patients favored SVZM classification with a hazard ratio (HR) for OS of 2.48 [95% CI 1.35-4.58], p = 0.004 vs. 1.83 [1.0-3.35], p = 0.049 for MRI classification. In the validation cohort, consensus MRI based assignment was achieved in 62% of patients with an intraclass correlation (ICC) of 0.51 and non-significant HR for OS (2.03 [0.81-5.09], p = 0.133). In contrast, SVZM identified two prognostically distinct subgroups (HR 3.08 [1.24-7.66], p = 0.016). CNV alterations revealed loss of chromosome 10 in SVZM- and gains on chromosome 19 in SVZM- tumors. SVZM- tumors were also enriched for differentially mutated genes (p < 0.001). In summary, SVZM classification provides a novel means for stratifying GBM patients with poor prognosis and deciphering molecular mechanisms governing aggressive tumor phenotypes.<br /> (© 2022. The Author(s).)
- Subjects :
- Adaptor Proteins, Signal Transducing genetics
DNA Copy Number Variations
Epigenome
Eye Proteins genetics
Humans
Intracellular Signaling Peptides and Proteins genetics
Lateral Ventricles diagnostic imaging
Lateral Ventricles pathology
Prognosis
Retrospective Studies
Brain Neoplasms diagnostic imaging
Brain Neoplasms genetics
Brain Neoplasms pathology
Glioblastoma diagnostic imaging
Glioblastoma genetics
Glioblastoma pathology
Subjects
Details
- Language :
- English
- ISSN :
- 1432-0533
- Volume :
- 144
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Acta neuropathologica
- Publication Type :
- Academic Journal
- Accession number :
- 35660939
- Full Text :
- https://doi.org/10.1007/s00401-022-02443-2