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

Acta Neuropathol Commun. 2024 Dec 20;12(1):195. doi: 10.1186/s40478-024-01896-8.

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.

Keywords: TRAF2; AYA; Genetic tumor syndromes; Medulloblastoma.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Cerebellar Neoplasms* / genetics
  • Cerebellar Neoplasms* / pathology
  • Female
  • Germ-Line Mutation*
  • Humans
  • Loss of Function Mutation
  • Male
  • Medulloblastoma* / genetics
  • Medulloblastoma* / pathology
  • TNF Receptor-Associated Factor 2* / genetics
  • TNF Receptor-Associated Factor 2* / metabolism
  • Young Adult

Substances

  • TNF Receptor-Associated Factor 2