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Status: Bibliographieeintrag

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Verfasst von:Korshunov, Andrey [VerfasserIn]   i
 Chavez, Lukas [VerfasserIn]   i
 Schrimpf, Daniel [VerfasserIn]   i
 Stichel, Damian [VerfasserIn]   i
 Capper, David [VerfasserIn]   i
 Sturm, Dominik [VerfasserIn]   i
 Kool, Marcel [VerfasserIn]   i
 Habel, Antje [VerfasserIn]   i
 Lichter, Peter [VerfasserIn]   i
 Pfister, Stefan [VerfasserIn]   i
 Jones, David T. W. [VerfasserIn]   i
 Deimling, Andreas von [VerfasserIn]   i
Titel:Epithelioid glioblastomas stratify into established diagnostic subsets upon integrated molecular analysis
Verf.angabe:Andrey Korshunov, Lukas Chavez, Tanvi Sharma, Marina Ryzhova, Daniel Schrimpf, Damian Stichel, David Capper, Dominik Sturm, Marcel Kool, Antje Habel, Bette K. Kleinschmidt‐DeMasters, Marc Rosenblum, Oksana Absalyamova, Andrey Golanov, Peter Lichter, Stefan M. Pfister, David T.W. Jones, Arie Perry, Andreas von Deimling
Jahr:2018
Umfang:7 S.
Teil:volume:28
 year:2018
 number:5
 pages:656-662
 extent:7
Fussnoten:First published: 09 October 2017 ; Gesehen am 22.01.2020
Titel Quelle:Enthalten in: Brain pathology
Ort Quelle:Oxford : Wiley-Blackwell, 1990
Jahr Quelle:2018
Band/Heft Quelle:28(2018), 5, Seite 656-662
ISSN Quelle:1750-3639
Abstract:Epithelioid glioblastoma (eGBM) is a newly defined and rare GBM variant in the current WHO 2016 classification. BRAF V600E mutation is overrepresented in these tumors and there is known some morphological overlap with anaplastic epithelioid PXA (ePXA). In order to further elucidate this diagnostic category, we molecularly characterized 64 pediatric and adult examples initially diagnosed as “eGBM.” Tumors were analyzed using array based methylation and direct sequencing of the BRAF and TERT genes. Our results demonstrated considerable molecular and clinical heterogeneity among eGBM cohort. Methylation patterns, copy number alterations, and mutational analysis data, in combination with clinical findings disclosed three different, well established tumor subtypes: (i) PXA-like tumors with favorable prognosis, predominantly in children and young adults (38), (ii) IDHwt GBM-like tumors with poor prognosis, mainly occurring in older adults, albeit with more frequent BRAF mutations (17), and (iii) RTK1 pediatric GBM-like neoplasms of intermediate prognosis in children and young adults, associated with chromothripsis and frequent PDGFRA amplifications (9). We conclude that the histopathologically defined eGBM do not represent a single diagnostic entity, but rather at least three molecularly and biologically distinct categories. Therefore, additional molecular testing through genome-wide molecular profiling is recommended to further stratify these rare cases.
DOI:doi:10.1111/bpa.12566
URL:Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.

Volltext ; Verlag: http://dx.doi.org/10.1111/bpa.12566
 Volltext: https://onlinelibrary.wiley.com/doi/abs/10.1111/bpa.12566
 DOI: https://doi.org/10.1111/bpa.12566
Datenträger:Online-Ressource
Sprache:eng
Sach-SW:cytogenetic prognostic
 epithelioid
 glioblastoma
 methylation
 pleomorphic xanthoastrocytoma
 subgroup
 survival
K10plus-PPN:1582259526
Verknüpfungen:→ Zeitschrift

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