Alternative lengthening of telomeres in molecular subgroups of paediatric high-grade glioma.


Journal

Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery
ISSN: 1433-0350
Titre abrégé: Childs Nerv Syst
Pays: Germany
ID NLM: 8503227

Informations de publication

Date de publication:
03 2021
Historique:
received: 07 04 2020
accepted: 16 10 2020
pubmed: 1 11 2020
medline: 29 6 2021
entrez: 31 10 2020
Statut: ppublish

Résumé

The maintenance of telomere length prevents cancer cell senescence and occurs via two mutually exclusive mechanisms: (a) reactivation of telomerase expression and (b) activation of alternative lengthening of telomeres (ALT). ALT is frequently related to alterations on ATRX, a chromatin-remodelling protein. Recent data have identified different molecular subgroups of paediatric high-grade glioma (pHGG) with mutations of H3F3A, TERTp and ATRX; however, differences in telomere length among these molecular subgroups were not thoroughly examined. We investigated which genetic alterations trigger the ALT mechanism in 52 IDH-wildtype, 1p/19q-wildtype pHGG. Samples were analysed for telomere length using Tel-FISH. ATRX nuclear loss of expression was assessed by IHC, H3F3A and TERTp mutations by DNA sequencing, and TERTp methylation by MS-PCR. Mutant H3.3 was found in 21 cases (40.3%): 19.2% with K27M mutation and 21.1% with G34R mutation. All H3.3G34R-mutated cases showed the ALT phenotype (100%); on the opposite, only 40% of the H3.3K27M-mutated showed ALT activation. ATRX nuclear loss was seen in 16 cases (30.7%), associated sometimes with the G34R mutation, and never with the K27M mutation. ATRX nuclear loss was always related to telomere elongation. TERTp C250T mutations were rare (5.4%) and were not associated with high intensity Tel-FISH signals, as TERTp hyper-methylation detected in 21% of the cases. H3.3/ATRX/TERTp-wildtype pHGG revealed all basal levels of telomere length. Our results show a strong association between H3.3 mutations and ALT, and highlight the different telomeric profiles in histone-defined subgroups: H3.3-G34R mutants always trigger ALT to maintain telomere length, irrespective of ATRX status, whereas only some H3.3-K27M tumours activate ALT. These findings suggest that acquiring the gly34 mutation on H3.3 might suffice to trigger the ALT mechanism.

Identifiants

pubmed: 33128602
doi: 10.1007/s00381-020-04933-8
pii: 10.1007/s00381-020-04933-8
pmc: PMC7875853
doi:

Substances chimiques

X-linked Nuclear Protein EC 3.6.4.12

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

809-818

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Auteurs

Simone Minasi (S)

Department of Radiological, Oncological and Anatomo-Pathological Sciences, Sapienza University of Rome, Rome, Italy.
Department of Human Neurosciences, Sapienza University of Rome, Rome, Italy.

Caterina Baldi (C)

Department of Human Neurosciences, Sapienza University of Rome, Rome, Italy.

Francesca Gianno (F)

Department of Radiological, Oncological and Anatomo-Pathological Sciences, Sapienza University of Rome, Rome, Italy.
Department of Molecular Medicine, Sapienza University of Rome, Rome, Italy.

Manila Antonelli (M)

Department of Radiological, Oncological and Anatomo-Pathological Sciences, Sapienza University of Rome, Rome, Italy.

Anna Maria Buccoliero (AM)

Pathology Unit, Meyer Children's University Hospital, I-50139, Florence, Italy.

Torsten Pietsch (T)

Institute of Neuropathology, DGNN Brain Tumour Reference Centre, University of Bonn Medical Centre, Bonn, Germany.

Maura Massimino (M)

Paediatric Unit, Fondazione IRCCS Istituto Nazionale dei Tumori, Milano, Italy.

Francesca Romana Buttarelli (FR)

Department of Radiological, Oncological and Anatomo-Pathological Sciences, Sapienza University of Rome, Rome, Italy. francesca.buttarelli@uniroma1.it.
Department of Human Neurosciences, Sapienza University of Rome, Rome, Italy. francesca.buttarelli@uniroma1.it.

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