Clinical and Molecular Characterization of Brazilian Patients Suspected to Have Lynch Syndrome

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da Silva, Felipe Carneiro ^[1] ; de Oliveira Ferreira, Jose Roberto ^[1] ; Torrezan, Giovana Tardin ^[1] ; Pena Figueiredo, Marcia Cristina ^[1] ; Monteiro Santos, Erika Maria ^[2] ; Nakagawa, Wilson Toshihiko ^[2] ; Brianese, Rafael Canfield ^[1] ; de Oliveira, Ligia Petrolini ^[2] ; Begnani, Maria Dirlei ^[3] ; Aguiar-Junior, Samuel ^[2] ; Rossi, Benedito Mauro ^[2] ; Ferreira, Fabio de Oliveira ^[2] ; Carraro, Dirce Maria ^{[4, 1]}

Afiliação do(s) autor(es)

^[1] AC Camargo Canc Ctr, Int Res Ctr CIPE, Lab Genom & Mol Biol, Sao Paulo - Brazil

^[2] AC Camargo Canc Ctr, Dept Colorectal Tumors, Sao Paulo - Brazil

^[3] AC Camargo Canc Ctr, Dept Anat Pathol, Sao Paulo - Brazil

^[4] Natl Inst Sci & Technol Oncogen INCITO, Sao Paulo - Brazil

• Tipo de documento: Artigo Científico
• Fonte: PLoS One; v. 10, n. 10 OCT 5 2015.
• Citações Web of Science: 11

Resumo

Lynch syndrome (LS) accounts for 3-5% of all colorectal cancers (CRC) and is inherited in an autosomal dominant fashion. This syndrome is characterized by early CRC onset, high incidence of tumors in the ascending colon, excess of synchronous/metachronous tumors and extra-colonic tumors. Nowadays, LS is regarded of patients who carry deleterious germline mutations in one of the five mismatch repair genes (MMR), mostly in MLH1 and MSH2, but also in MSH6, PMS1 and PMS2. To comprehensively characterize 116 Brazilian patients suspected for LS, we assessed the frequency of germline mutations in the three minor genes MSH6, PMS1 and PMS2 in 82 patients negative for point mutations in MLH1 and MSH2. We also assessed large genomic rearrangements by MLPA for detecting copy number variations (CNVs) in MLH1, MSH2 and MSH6 generating a broad characterization of MMR genes. The complete analysis of the five MMR genes revealed 45 carriers of pathogenic mutations, including 25 in MSH2, 15 in MLH1, four in MSH6 and one in PMS2. Eleven novel pathogenic mutations (6 in MSH2, 4 in MSH6 and one in PMS2), and 11 variants of unknown significance (VUS) were found. Mutations in the MLH1 and MSH2 genes represented 89% of all mutations (40/45), whereas the three MMR genes (MSH6, PMS1 and PMS2) accounted for 11% (5/45). We also investigated the MLH1 p. Leu676Pro VUS located in the PMS2 interaction domain and our results revealed that this variant displayed no defective function in terms of cellular location and heterodimer interaction. Additionally, we assessed the tumor phenotype of a subset of patients and also the frequency of CRC and extra-colonic tumors in 2,365 individuals of the 116 families, generating the first comprehensive portrait of the genetic and clinical aspects of patients suspected of LS in a Brazilian cohort. (AU)

• Processo FAPESP: 08/57887-9 - Instituto Nacional de Oncogenômica
• Beneficiário: Luiz Paulo Kowalski
• Modalidade de apoio: Auxílio à Pesquisa - Temático