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1000 Titel
  • Malignant gliomas with H3F3A G34R mutation or MYCN amplification in pediatric patients with Li Fraumeni syndrome
1000 Autor/in
  1. Schoof, Melanie |
  2. Kordes, Uwe |
  3. Volk, Alexander E. |
  4. Al-Kershi, Sina |
  5. Kresbach, Catena |
  6. Schüller, Ulrich |
1000 Erscheinungsjahr 2021
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2021-07-15
1000 Erschienen in
1000 Quellenangabe
  • 142(3):591-593
1000 Copyrightjahr
  • 2021
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1007/s00401-021-02346-8 |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8357758/ |
1000 Publikationsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • Subependymomas are benign tumors characteristically encountered in the posterior fossa of adults that show distinct epigenetic profiles assigned to the molecular group 'subependymoma, posterior fossa' (PFSE) of the recently established DNA methylation-based classification of central nervous system tumors. In contrast, most posterior fossa ependymomas exhibit a more aggressive biological behavior and are allocated to the molecular subgroups PFA or PFB. A subset of ependymomas shows epigenetic similarities with subependymomas, but the precise biology of these tumors and their potential relationships remain unknown. We therefore set out to characterize epigenetic traits, mutational profiles, and clinical outcomes of 50 posterior fossa ependymal tumors of the PFSE group. On histo-morphology, these tumors comprised 12 ependymomas, 14 subependymomas and 24 tumors with mixed ependymoma-subependymoma morphology. Mixed ependymoma-subependymoma tumors varied in their extent of ependymoma differentiation (2-95%) but consistently exhibited global epigenetic profiles of the PFSE group. Selective methylome analysis of microdissected tumor components revealed CpG signatures in mixed tumors that coalesce with their pure counterparts. Loss of chr6 (20/50 cases), as well as TERT mutations (21/50 cases), were frequent events enriched in tumors with pure ependymoma morphology (p < 0.001) and confined to areas with ependymoma differentiation in mixed tumors. Clinically, pure ependymoma phenotype, chr6 loss, and TERT mutations were associated with shorter progression-free survival (each p < 0.001). In conclusion, our results suggest that subependymomas may acquire genetic and epigenetic changes throughout tumor evolution giving rise to subclones with ependymoma morphology (resulting in mixed tumors) that eventually overpopulate the subependymoma component (pure PFSE ependymomas).
1000 Sacherschließung
lokal Mutation/genetics [MeSH]
lokal Adolescent [MeSH]
lokal Brain Neoplasms/genetics [MeSH]
lokal N-Myc Proto-Oncogene Protein/genetics [MeSH]
lokal Histones/genetics [MeSH]
lokal Humans [MeSH]
lokal Gene Amplification [MeSH]
lokal Li-Fraumeni Syndrome/genetics [MeSH]
lokal Glioma/pathology [MeSH]
lokal Male [MeSH]
lokal Germ-Line Mutation [MeSH]
lokal Glioma/genetics [MeSH]
lokal Pathology
lokal Neurosciences
lokal Correspondence
lokal Brain Neoplasms/pathology [MeSH]
1000 Liste der Beteiligten
  1. https://frl.publisso.de/adhoc/uri/U2Nob29mLCBNZWxhbmll|https://frl.publisso.de/adhoc/uri/S29yZGVzLCBVd2U=|https://frl.publisso.de/adhoc/uri/Vm9saywgQWxleGFuZGVyIEUu|https://frl.publisso.de/adhoc/uri/QWwtS2Vyc2hpLCBTaW5h|https://frl.publisso.de/adhoc/uri/S3Jlc2JhY2gsIENhdGVuYQ==|https://orcid.org/0000-0002-8731-1121
1000 Hinweis
  • DeepGreen-ID: 67276e662d4541fbb08761b67fc51a89 ; metadata provieded by: DeepGreen (https://www.oa-deepgreen.de/api/v1/), LIVIVO search scope life sciences (http://z3950.zbmed.de:6210/livivo), Crossref Unified Resource API (https://api.crossref.org/swagger-ui/index.html), to.science.api (https://frl.publisso.de/), ZDB JSON-API (beta) (https://zeitschriftendatenbank.de/api/), lobid - Dateninfrastruktur für Bibliotheken (https://lobid.org/resources/search)
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1000 Erstellt am 2023-05-11T10:37:05.396+0200
1000 Erstellt von 322
1000 beschreibt frl:6450706
1000 Zuletzt bearbeitet Sat Oct 14 08:53:10 CEST 2023
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