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The Brazilian TP53 mutation (R337H) and sarcomas.
Volc, Sahlua Miguel; Ramos, Cíntia Regina Niederauer; Galvão, Henrique de Campos Reis; Felicio, Paula Silva; Coelho, Aline Silva; Berardineli, Gustavo Noriz; Campacci, Natalia; Sabato, Cristina da Silva; Abrahao-Machado, Lucas Faria; Santana, Iara Viana Vidigal; Campanella, Nathalia; Lengert, André van Helvoort; Vidal, Daniel Onofre; Reis, Rui Manuel; Dantas, Caio F; Coelho, Robson C; Boldrini, Erica; Serrano, Sergio Vicente; Palmero, Edenir Inêz.
Afiliação
  • Volc SM; Oncogenetics Department, Barretos Cancer Hospital, Barretos, São Paulo, Brazil.
  • Ramos CRN; Molecular Oncology Research Center, Barretos Cancer Hospital, Barretos, São Paulo, Brazil.
  • Galvão HCR; Oncogenetics Department, Barretos Cancer Hospital, Barretos, São Paulo, Brazil.
  • Felicio PS; Molecular Oncology Research Center, Barretos Cancer Hospital, Barretos, São Paulo, Brazil.
  • Coelho AS; Molecular Oncology Research Center, Barretos Cancer Hospital, Barretos, São Paulo, Brazil.
  • Berardineli GN; Center of Molecular Diagnosis, Barretos Cancer Hospital, Barretos, São Paulo, Brazil.
  • Campacci N; Molecular Oncology Research Center, Barretos Cancer Hospital, Barretos, São Paulo, Brazil.
  • Sabato CDS; Center of Molecular Diagnosis, Barretos Cancer Hospital, Barretos, São Paulo, Brazil.
  • Abrahao-Machado LF; Pathology Department, Barretos Cancer Hospital, Barretos, São Paulo, Brazil.
  • Santana IVV; Pathology Department, Barretos Cancer Hospital, Barretos, São Paulo, Brazil.
  • Campanella N; Molecular Oncology Research Center, Barretos Cancer Hospital, Barretos, São Paulo, Brazil.
  • Lengert AVH; Molecular Oncology Research Center, Barretos Cancer Hospital, Barretos, São Paulo, Brazil.
  • Vidal DO; Barretos Children's Cancer Hospital, Barretos, São Paulo, Brazil.
  • Reis RM; Molecular Oncology Research Center, Barretos Cancer Hospital, Barretos, São Paulo, Brazil.
  • Dantas CF; Molecular Oncology Research Center, Barretos Cancer Hospital, Barretos, São Paulo, Brazil.
  • Coelho RC; Center of Molecular Diagnosis, Barretos Cancer Hospital, Barretos, São Paulo, Brazil.
  • Boldrini E; Life and Health Sciences Research Institute (ICVS), Health Sciences School, University of Minho, Braga, Portugal.
  • Serrano SV; ICVS/3B's-PT Government Associate Laboratory, Braga/Guimarães, Portugal.
  • Palmero EI; Clinical Oncology Department, Barretos Cancer Hospital, Barretos, São Paulo, Brazil.
PLoS One ; 15(1): e0227260, 2020.
Article em En | MEDLINE | ID: mdl-31978118
ABSTRACT
Sarcomas represent less than 1% of all solid neoplasms in adults and over 20% in children. Their etiology is unclear, but genetic susceptibility plays an important role in this scenario. Sarcoma is central in Li-Fraumeni Syndrome (LFS), a familial predisposition cancer syndrome. In Brazil, the high prevalence of p.Arg337His mutations in the TP53 gene brings about a unique condition a cluster of LFS. In the present work, we studied 502 sarcoma patients not selected by age or family history in an attempt to assess the impact of the so-called "Brazilian germline TP53 mutation" (p.Arg337His) on this tumor type. We found that 8% of patients are carriers, with leiomyosarcoma being the main histologic type of sarcoma, corresponding to 52.5% of the patients with the mutated TP53 gene. These findings emphasize the importance of genetic counseling and can better guide the management of sarcoma patients.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Sarcoma / Proteína Supressora de Tumor p53 / Síndrome de Li-Fraumeni / Predisposição Genética para Doença Tipo de estudo: Diagnostic_studies / Prevalence_studies / Risk_factors_studies Limite: Adolescent / Adult / Aged / Aged80 / Female / Humans / Male / Middle aged País/Região como assunto: America do sul / Brasil Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Sarcoma / Proteína Supressora de Tumor p53 / Síndrome de Li-Fraumeni / Predisposição Genética para Doença Tipo de estudo: Diagnostic_studies / Prevalence_studies / Risk_factors_studies Limite: Adolescent / Adult / Aged / Aged80 / Female / Humans / Male / Middle aged País/Região como assunto: America do sul / Brasil Idioma: En Ano de publicação: 2020 Tipo de documento: Article