Supratentorial ependymoma in childhood: more than just RELA or YAP.


Journal

Acta neuropathologica
ISSN: 1432-0533
Titre abrégé: Acta Neuropathol
Pays: Germany
ID NLM: 0412041

Informations de publication

Date de publication:
03 2021
Historique:
received: 19 11 2020
accepted: 24 12 2020
revised: 24 12 2020
pubmed: 23 1 2021
medline: 6 11 2021
entrez: 22 1 2021
Statut: ppublish

Résumé

Two distinct genetically defined entities of ependymoma arising in the supratentorial compartment are characterized by the presence of either a C11orf95-RELA or a YAP-MAMLD1 fusion, respectively. There is growing evidence that supratentorial ependymomas without these genetic features exist. In this study, we report on 18 pediatric non-RELA/non-YAP supratentorial ependymomas that were systematically characterized by means of their histology, immunophenotype, genetics, and epigenomics. Comprehensive molecular analyses included high-resolution copy number analysis, methylation profiling, analysis of fusion transcripts by Nanostring technology, and RNA sequencing. Based upon histological and immunohistochemical features two main patterns were identified-RELA-like (n = 9) and tanycytic ependymomas (n = 6). In the RELA-like group histologically assigned to WHO grade III and resembling RELA-fused ependymomas, tumors lacked nuclear expression of p65-RelA as a surrogate marker for a pathological activation of the NF-κB pathway. Three tumors showed alternative C11orf95 fusions to MAML2 or NCOA1. A methylation-based brain tumor classifier assigned two RELA-like tumors to the methylation class "EP, RELA-fusion"; the others demonstrated no significant similarity score. Of the tanycytic group, 5/6 tumors were assigned a WHO grade II. No gene fusions were detected. Methylation profiling did not show any association with an established methylation class. We additionally identified two astroblastoma-like tumors that both presented with chromothripsis of chromosome 22 but lacked MN1 breaks according to FISH analysis. They revealed novel fusion events involving genes in chromosome 22. One further tumor with polyploid cytogenetics was interpreted as PFB ependymoma by the brain tumor methylation classifier but had no relation to the posterior fossa. Clinical follow-up was available for 16/18 patients. Patients with tanycytic and astroblastoma-like tumors had no relapse, while 2 patients with RELA-like ependymomas died. Our data indicate that in addition to ependymomas discovered so far, at least two more supratentorial ependymoma types (RELA-like and tanycytic) exist.

Identifiants

pubmed: 33481105
doi: 10.1007/s00401-020-02260-5
pii: 10.1007/s00401-020-02260-5
pmc: PMC7882569
doi:

Substances chimiques

Adaptor Proteins, Signal Transducing 0
RELA protein, human 0
Transcription Factor RelA 0
Transcription Factors 0
YAP-Signaling Proteins 0
YAP1 protein, human 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

455-466

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Auteurs

Valentina Zschernack (V)

Department of Neuropathology, DGNN Brain Tumor Reference Center, University of Bonn Medical Center, Venusberg-Campus 1, 53127, Bonn, Germany.

Stephanie T Jünger (ST)

Department of Neuropathology, DGNN Brain Tumor Reference Center, University of Bonn Medical Center, Venusberg-Campus 1, 53127, Bonn, Germany.
Department of Neurosurgery, University of Cologne Medical Center, Cologne, Germany.

Martin Mynarek (M)

Department of Pediatric Oncology and Hematology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

Stefan Rutkowski (S)

Department of Pediatric Oncology and Hematology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

Maria Luisa Garre (ML)

Neuro-Oncology Unit, IRCCS Istituto Giannina Gaslini, Genoa, Italy.

Martin Ebinger (M)

Department of Pediatric Hematology and Oncology, University Hospital Tübingen, Tübingen, Germany.

Marie Neu (M)

Department of Pediatric Hematology/Oncology, Center for Pediatric and Adolescent Medicine, University Medical Center of the Johannes Gutenberg-University Mainz, Mainz, Germany.

Jörg Faber (J)

Department of Pediatric Hematology/Oncology, Center for Pediatric and Adolescent Medicine, University Medical Center of the Johannes Gutenberg-University Mainz, Mainz, Germany.

Bernhard Erdlenbruch (B)

Johannes Wesling Klinikum Minden, University Hospital for Children and Adolescents, Ruhr University Hospital, Bochum, Germany.

Alexander Claviez (A)

Department of Pediatric and Adolescent Medicine, Pediatric Hematology and Oncology, University Hospital Schleswig Holstein, Kiel, Germany.

Stefan Bielack (S)

Department of Pediatric Oncology, Hematology and Immunology, Center for Pediatric, Adolescent and Women's Medicine, Stuttgart Cancer Center, Klinikum Stuttgart-Olgahospital, Stuttgart, Germany.

Triantafyllia Brozou (T)

Department of Pediatric Oncology, Hematology and Clinical Immunology, University Children's Hospital Medical Faculty, Heinrich-Heine-University, Düsseldorf, Germany.

Michael C Frühwald (MC)

University Medical Center Augsburg, Swabian Children's Cancer Center, Augsburg, Germany.

Evelyn Dörner (E)

Department of Neuropathology, DGNN Brain Tumor Reference Center, University of Bonn Medical Center, Venusberg-Campus 1, 53127, Bonn, Germany.

Verena Dreschmann (V)

Department of Neuropathology, DGNN Brain Tumor Reference Center, University of Bonn Medical Center, Venusberg-Campus 1, 53127, Bonn, Germany.

Annika Stock (A)

Department of Neuroradiology, University Hospital Würzburg, Würzburg, Germany.

Laszlo Solymosi (L)

Department of Neuroradiology, University Hospital Würzburg, Würzburg, Germany.

Jürgen Hench (J)

Division of Neuropathology, Department of Medical Genetics and Pathology, University Hospital Basel, Basel, Switzerland.

Stephan Frank (S)

Division of Neuropathology, Department of Medical Genetics and Pathology, University Hospital Basel, Basel, Switzerland.

Christian Vokuhl (C)

Pediatric Pathology, Department of Pathology, University of Bonn Medical Center, Bonn, Germany.

Andreas Waha (A)

Department of Neuropathology, DGNN Brain Tumor Reference Center, University of Bonn Medical Center, Venusberg-Campus 1, 53127, Bonn, Germany.

Felipe Andreiuolo (F)

Department of Neuropathology, DGNN Brain Tumor Reference Center, University of Bonn Medical Center, Venusberg-Campus 1, 53127, Bonn, Germany.
Instituto Estadual Do Cérebro Paulo Niemeyer and the IDOR Institute, Rio de Janeiro, Brazil.

Torsten Pietsch (T)

Department of Neuropathology, DGNN Brain Tumor Reference Center, University of Bonn Medical Center, Venusberg-Campus 1, 53127, Bonn, Germany. t.pietsch@uni-bonn.de.

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Classifications MeSH