| Literature DB >> 18248785 |
Edenir Inêz Palmero1, Lavínia Schüler-Faccini, Maira Caleffi, Maria Isabel Waddington Achatz, Magali Olivier, Ghyslaine Martel-Planche, Virginie Marcel, Ernestina Aguiar, Juliana Giacomazzi, Ingrid Petroni Ewald, Roberto Giugliani, Pierre Hainaut, Patricia Ashton-Prolla.
Abstract
Germline TP53 mutations predispose to a rare familial cancer syndrome, the Li-Fraumeni Syndrome (LFS), characterized by the early onset of multiple cancers including childhood adrenocortical carcinomas, sarcomas and brain tumors, and breast and colon cancer in young adults. An identical germline mutation at codon 337 in TP53 (R337H) has been shown to be causally related to an increased risk of multiple cancers in unrelated subjects with familial cancer risk in Southern Brazil. Here we have assessed the prevalence of R337H in 750 healthy women participating in a community-based breast cancer screening program in the area of Porto Alegre. The mutant was detected in two participants (0.3%) who were fourth-degree relatives and reported a familial history of cancer at multiple sites that did not match classical criteria for LFS and its variants. Testing in additional family members detected the mutation in three subjects, one of whom developed breast cancer at the age of 36. These findings indicate that R337H may be a low penetrance mutant which predisposes to multiple cancers and occurs in the population of Southern Brazil at a frequency 10-20 times higher than other TP53 mutants commonly associated with LFS.Entities:
Mesh:
Year: 2008 PMID: 18248785 DOI: 10.1016/j.canlet.2007.10.044
Source DB: PubMed Journal: Cancer Lett ISSN: 0304-3835 Impact factor: 8.679