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Histone H3 wild-type DIPG/DMG overexpressing EZHIP extend the spectrum diffuse midline gliomas with PRC2 inhibition beyond H3-K27M mutation.

Authors :
Castel, David
Kergrohen, Thomas
Tauziède-Espariat, Arnault
Mackay, Alan
Ghermaoui, Samia
Lechapt, Emmanuèle
Pfister, Stefan M.
Kramm, Christof M.
Boddaert, Nathalie
Blauwblomme, Thomas
Puget, Stéphanie
Beccaria, Kévin
Jones, Chris
Jones, David T. W.
Varlet, Pascale
Grill, Jacques
Debily, Marie-Anne
Source :
Acta Neuropathologica; Jun2020, Vol. 139 Issue 6, p1109-1113, 5p
Publication Year :
2020

Abstract

2 Molecular and clinical portrait of H3 wild-type DMG patients. a Clinicopathological and molecular annotations are provided as bars for 19 histone H3 wild-type DMG patients. Samples are arranged in columns with genes labeled along rows. b Distribution of normalized EZHIP gene expression level, in H3-K27M (green, n = 20) and H3 wild-type (grey, n = 11) DMG patients. We propose that these EZHIP/H3-WT tumors need to be considered similar to canonical DIPG/DMG, thus extending the spectrum of DMG with PRC2 inhibition beyond H3-K27M mutation. [Extracted from the article]

Details

Language :
English
ISSN :
00016322
Volume :
139
Issue :
6
Database :
Complementary Index
Journal :
Acta Neuropathologica
Publication Type :
Academic Journal
Accession number :
143387732
Full Text :
https://doi.org/10.1007/s00401-020-02142-w