Structural variants shape driver combinations and outcomes in pediatric high-grade glioma.
Journal
Nature cancer
ISSN: 2662-1347
Titre abrégé: Nat Cancer
Pays: England
ID NLM: 101761119
Informations de publication
Date de publication:
08 2022
08 2022
Historique:
received:
30
10
2021
accepted:
23
05
2022
pubmed:
6
7
2022
medline:
27
8
2022
entrez:
5
7
2022
Statut:
ppublish
Résumé
We analyzed the contributions of structural variants (SVs) to gliomagenesis across 179 pediatric high-grade gliomas (pHGGs). The most recurrent SVs targeted MYC isoforms and receptor tyrosine kinases (RTKs), including an SV amplifying a MYC enhancer in 12% of diffuse midline gliomas (DMG), indicating an underappreciated role for MYC in pHGG. SV signature analysis revealed that tumors with simple signatures were TP53 wild type (TP53
Identifiants
pubmed: 35788723
doi: 10.1038/s43018-022-00403-z
pii: 10.1038/s43018-022-00403-z
pmc: PMC10365847
mid: NIHMS1907773
doi:
Substances chimiques
Cell Cycle Proteins
0
Histones
0
MDM4 protein, human
0
Proto-Oncogene Proteins
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Research Support, N.I.H., Extramural
Langues
eng
Sous-ensembles de citation
IM
Pagination
994-1011Subventions
Organisme : NCI NIH HHS
ID : R01 CA188228
Pays : United States
Organisme : Cancer Research UK
ID : 13982
Pays : United Kingdom
Organisme : NCI NIH HHS
ID : R01 CA219943
Pays : United States
Organisme : NCI NIH HHS
ID : R01 CA215489
Pays : United States
Organisme : NCI NIH HHS
ID : R37 CA255245
Pays : United States
Organisme : NCI NIH HHS
ID : P30 CA015083
Pays : United States
Commentaires et corrections
Type : CommentIn
Informations de copyright
© 2022. The Author(s), under exclusive licence to Springer Nature America, Inc.
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