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(Referência obtida automaticamente do Web of Science, por meio da informação sobre o financiamento pela FAPESP e o número do processo correspondente, incluída na publicação pelos autores.)

High Prevalence of EGFR Mutations in Lung Adenocarcinomas From Brazilian Patients Harboring the TP53 p.R337H Variant

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Autor(es):
Barbosa, Malu Viter R. [1] ; Cordeiro de Lima, Vladmir C. [1, 2] ; Formiga, Maria Nirvana [1] ; Andrade de Paula, Claudia A. [3] ; Torrezan, Giovana T. [4, 3] ; Carraro, Dirce M. [4, 3]
Número total de Autores: 6
Afiliação do(s) autor(es):
[1] AC Camargo Canc Ctr, Med Oncol Dept, R Prof Antonio Prudente 211, BR-01509900 Sao Paulo, SP - Brazil
[2] AC Camargo Canc Ctr, Translat Immunooncol Lab, Int Res Ctr, Sao Paulo - Brazil
[3] AC Camargo Canc Ctr, Genom & Mol Biol Lab, CIPE, R Tagua 440, BR-01508010 Sao Paulo, SP - Brazil
[4] Natl Inst Sci & Technol Oncogen INCITO, Sao Paulo - Brazil
Número total de Afiliações: 4
Tipo de documento: Artigo Científico
Fonte: CLINICAL LUNG CANCER; v. 21, n. 2, p. E37-E44, MAR 2020.
Citações Web of Science: 0
Resumo

Lung cancer represents around 3.6% of all Li-Fraumeni syndrome-associated tumors. A high prevalence of p.R337H germline mutation in the TP53 gene has been observed in Brazil and family histories of cancer associated with this variant range from isolated cases to families fulfilling Li-Fraumenielike or Li-Fraumeni criteria. We evaluated the frequency of EGFR mutations in lung adenocarcinoma (LA) diagnosed in Brazilian patients carrying the TP53 founder mutation p.R337H, as well as the frequency of TP53 p.R337H mutation among LA cases with EGFR mutation. Patients diagnosed with LA were selected from a total of 164 TP53 p.R337H mutation carriers followed at A. C. Camargo Cancer Center. Tumor samples were submitted to EGFR hot-spot mutation sequencing. TP53 p.R337H was genotyped in a cohort of 257 LA tumor samples, 114 with and 143 without EGFR activating mutations. The frequency of LA among TP53 p.R337H carriers was 5.4% (9/164), and EGFR mutations were detected in 89% (8/9) of these patients. The prevalence of TP53 variants at codon 337 in patients with LA harboring EGFR activating mutations was 5.3% (6/114-5 p.R337H and 1 p.R337C) and 12.5% (4/32) in LA tumors diagnosed at any age and before the age of 50 years, respectively. This prevalence was significantly higher than that in the cohort of LA tumors with no EGFR activating mutation (1/143 in LA diagnosed at any age, 0/34 in LA diagnosed before the age of 50 years). There is a higher than expected frequency of EGFR activating mutations in LA Brazilian patients with TP53 p.R337H mutation. The high frequency of p.R337H/C carriers among patients with EGFR-mutated LA indicates that TP53 genetic testing should be recommended to these patients, regardless of whether they fulfill Li-Fraumeni syndrome/Li-Fraumenie-like criteria or have no defined cancer risk criteria. (C) 2019 The Author(s). Published by Elsevier Inc. (AU)

Processo FAPESP: 13/23277-8 - Aspectos moleculares envolvidos no risco, desenvolvimento e progressão do carcinoma ductal de mama: busca de novos genes de susceptibilidade e investigação da progressão do carcinoma in situ e do papel da mutação em BRCA1 no tumor triplo negativo
Beneficiário:Dirce Maria Carraro
Linha de fomento: Auxílio à Pesquisa - Temático