Germline loss-of-function variant in the E3 ubiquitin ligase TRAF2 in a young adult patient with medulloblastoma: a case report

We identified a rare heterozygous germline loss-of-function variant in the tumor necrosis factor receptor-associated factor 2 (TRAF2) in a young adult patient diagnosed with medulloblastoma. This variant is located within the TRAF-C domain of the E3 ubiquitin ligase protein and is predicted to diminish the binding affinity of TRAF2 to upstream receptors and associated adaptor proteins. Integrative genomics revealed a biallelic loss of TRAF2 via partial copy-neutral loss-of-heterozygosity of 9q in the medulloblastoma genome. We further performed comparative analysis with an in-house cohort of 20 medulloblastomas sequenced using the same platform, revealing an atypical molecular profile of the TRAF2-associated medulloblastoma. Our research adds to the expanding catalog of genetic tumor syndromes that increase the susceptibility of carriers to MB.

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Publication Details

Journal
Acta Neuropathologica Communications
Published
2024-12-20
DOI
https://doi.org/10.1186/s40478-024-01896-8
Primary Topic
NF-κB Signaling Pathways
Type
article
Field-Weighted Citation Impact
0.00

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article

Germline loss-of-function variant in the E3 ubiquitin ligase TRAF2 in a young adult patient with medulloblastoma: a case report

Arul M. Chinnaiyan, Nicole A. Becker, Sebastian M. Waszak, Andrea T. Franson et al.
Acta Neuropathologica Communications
NF-κB Signaling Pathways
article

Germline loss-of-function variant in the E3 ubiquitin ligase TRAF2 in a young adult patient with medulloblastoma: a case report

Arul M. Chinnaiyan, Nicole A. Becker, Sebastian M. Waszak, Andrea T. Franson, Dan R. Robinson, Yi-Mi Wu, Josh N. Vo
article en

Abstract

We identified a rare heterozygous germline loss-of-function variant in the tumor necrosis factor receptor-associated factor 2 (TRAF2) in a young adult patient diagnosed with medulloblastoma. This variant is located within the TRAF-C domain of the E3 ubiquitin ligase protein and is predicted to diminish the binding affinity of TRAF2 to upstream receptors and associated adaptor proteins. Integrative genomics revealed a biallelic loss of TRAF2 via partial copy-neutral loss-of-heterozygosity of 9q in the medulloblastoma genome. We further performed comparative analysis with an in-house cohort of 20 medulloblastomas sequenced using the same platform, revealing an atypical molecular profile of the TRAF2-associated medulloblastoma. Our research adds to the expanding catalog of genetic tumor syndromes that increase the susceptibility of carriers to MB.

Acta Neuropathologica CommunicationsVol. 12(1)
University of California, San Francisco (US), University of Michigan (US), Michigan Medicine (US), Michigan Center for Translational Pathology (US), École Polytechnique Fédérale de Lausanne (CH)
American Cancer Society
Good health and well-being
Openalex Percentile: Top 67%
NF-κB Signaling Pathways
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Germline loss-of-function variant in the E3 ubiquitin ligase TRAF2 in a young adult patient with medulloblastoma: a case report — Arul M. Chinnaiyan, Nicole A. Becker, et al. · Acta Neuropathologica Communications (2024) | TGRS Research Map | TGRS