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CHEK2 is not a Li-Fraumeni syndrome gene: time to update public resources.
Fortuno, Cristina; Richardson, Marcy; Pesaran, Tina; Yussuf, Amal; Horton, Carolyn; James, Paul A; Spurdle, Amanda B.
Afiliación
  • Fortuno C; Population Health Program, QIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia.
  • Richardson M; Ambry Genetics, Aliso Viejo, California, USA.
  • Pesaran T; Ambry Genetics, Aliso Viejo, California, USA.
  • Yussuf A; Ambry Genetics, Aliso Viejo, California, USA.
  • Horton C; Ambry Genetics, Aliso Viejo, California, USA.
  • James PA; Parkville Familial Cancer Centre, Peter MacCallum Cancer Centre and Royal Melbourne Hospital, Melbourne, Victoria, Australia.
  • Spurdle AB; Sir Peter MacCallum Department of Oncology, University of Melbourne, Melbourne, Victoria, Australia.
J Med Genet ; 60(12): 1215-1217, 2023 Nov 27.
Article en En | MEDLINE | ID: mdl-37536919
The gene-disease relationship for CHEK2 remains listed as 'Li-Fraumeni syndrome 2' in public resources such as OMIM and MONDO, despite published evidence to the contrary, causing frustration among Li-Fraumeni syndrome (LFS) clinical experts. Here, we compared personal cancer characteristics of 2095 CHEK2 and 248 TP53 pathogenic variant carriers undergoing multigene panel testing at Ambry Genetics against 15 135 individuals with no known pathogenic variant. Our results from a within-cohort logistic regression approach highlight obvious differences between clinical presentation of TP53 and CHEK2 pathogenic variant carriers, with no evidence of CHEK2 being associated with any of the TP53-related core LFS cancers. These findings emphasise the need to replace 'Li-Fraumeni syndrome 2' as the CHEK2-associated disease name, thereby limiting potential confusion.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Síndrome de Li-Fraumeni Límite: Humans Idioma: En Revista: J Med Genet Año: 2023 Tipo del documento: Article País de afiliación: Australia Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Síndrome de Li-Fraumeni Límite: Humans Idioma: En Revista: J Med Genet Año: 2023 Tipo del documento: Article País de afiliación: Australia Pais de publicación: Reino Unido