E-Cadherin (CDH1) and p53 rather than SMAD4 and Caspase-10 germline mutations contribute to genetic predisposition in Portuguese gastric cancer patients

Bibliographic Details
Main Author: Oliveira, Carla
Publication Date: 2004
Other Authors: Ferreira, Paulo, Nabais, Sérgio, Campos, Luísa, Ferreira, Ana, Cirnes, Luís, Alves, Catarina Castro, Veiga, Isabel, Fragoso, Maria, Regateiro, Fernando, Dias, Luís Moreira, Moreira, Herculano, Suriano, Gianpaolo, Machado, José Carlos, Lopes, Carlos, Castedo, Sérgio, Carneiro, Fátima, Seruca, Raquel
Format: Article
Language: eng
Source: Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
Download full: https://hdl.handle.net/10316/4780
Summary: Approximately 30% of all hereditary diffuse gastric cancer (HDGC) families carry CDH1 germline mutations. The other two thirds remain genetically unexplained and are probably caused by alterations in other genes. Using polymerase chain reaction (PCR)/single-strand conformation polymorphism (SSCP)/sequencing, we screened 32 Portuguese families with a history of gastric cancer and 23 patients with early onset gastric cancer for CDH1 germline mutations. In probands negative for CDH1 mutations, we screened genes involved in hereditary cancer syndromes in which gastric cancer may be one of the component tumours, namely p53 (Li-Fraumeni Syndrome) and hMLH1 and hMSH2 (HNPCC). We also screened in these patients for mutations in Caspase-10, a gene inactivated in sporadic gastric cancer, and SMAD4, a gene whose inactivation in mice is associated with signet-ring cell carcinoma of the stomach. One of the families fulfilling the HDGC criteria harboured a CDH1 germline mutation, and one of the families with incomplete criteria harboured a p53 germline mutation. No mutations were identified in hMLH1 and hMSH2, and only sequence variants were found in SMAD4 and Caspase-10. The present work reports for the first time CDH1 germline mutations in Portuguese gastric cancer families, and highlights the need for p53 mutation screening in families lacking CDH1 germline mutations, in a country with one of the highest incidences of gastric cancer in the world. No evidence was found for a role of germline mutations in SMAD4 and Caspase-10 in families lacking CDH1 mutations.
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spelling E-Cadherin (CDH1) and p53 rather than SMAD4 and Caspase-10 germline mutations contribute to genetic predisposition in Portuguese gastric cancer patientsE-cadherin germline mutationsFamilial gastric cancerHereditary diffuse gastric cancerp53 germline mutationsLi-Fraumeni syndromeSMAD4 mutationsCaspase-10 mutationsApproximately 30% of all hereditary diffuse gastric cancer (HDGC) families carry CDH1 germline mutations. The other two thirds remain genetically unexplained and are probably caused by alterations in other genes. Using polymerase chain reaction (PCR)/single-strand conformation polymorphism (SSCP)/sequencing, we screened 32 Portuguese families with a history of gastric cancer and 23 patients with early onset gastric cancer for CDH1 germline mutations. In probands negative for CDH1 mutations, we screened genes involved in hereditary cancer syndromes in which gastric cancer may be one of the component tumours, namely p53 (Li-Fraumeni Syndrome) and hMLH1 and hMSH2 (HNPCC). We also screened in these patients for mutations in Caspase-10, a gene inactivated in sporadic gastric cancer, and SMAD4, a gene whose inactivation in mice is associated with signet-ring cell carcinoma of the stomach. One of the families fulfilling the HDGC criteria harboured a CDH1 germline mutation, and one of the families with incomplete criteria harboured a p53 germline mutation. No mutations were identified in hMLH1 and hMSH2, and only sequence variants were found in SMAD4 and Caspase-10. The present work reports for the first time CDH1 germline mutations in Portuguese gastric cancer families, and highlights the need for p53 mutation screening in families lacking CDH1 germline mutations, in a country with one of the highest incidences of gastric cancer in the world. No evidence was found for a role of germline mutations in SMAD4 and Caspase-10 in families lacking CDH1 mutations.http://www.sciencedirect.com/science/article/B6T68-4CP0YVH-5/1/0b2a789fc5dbe341d589aa4cee90b9ec2004info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleaplication/PDFhttps://hdl.handle.net/10316/4780https://hdl.handle.net/10316/4780engEuropean Journal of Cancer. 40:12 (2004) 1897-1903Oliveira, CarlaFerreira, PauloNabais, SérgioCampos, LuísaFerreira, AnaCirnes, LuísAlves, Catarina CastroVeiga, IsabelFragoso, MariaRegateiro, FernandoDias, Luís MoreiraMoreira, HerculanoSuriano, GianpaoloMachado, José CarlosLopes, CarlosCastedo, SérgioCarneiro, FátimaSeruca, Raquelinfo:eu-repo/semantics/openAccessreponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiainstacron:RCAAP2021-10-15T14:31:21Zoai:estudogeral.uc.pt:10316/4780Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireinfo@rcaap.ptopendoar:https://opendoar.ac.uk/repository/71602025-05-29T04:54:41.050269Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiafalse
dc.title.none.fl_str_mv E-Cadherin (CDH1) and p53 rather than SMAD4 and Caspase-10 germline mutations contribute to genetic predisposition in Portuguese gastric cancer patients
title E-Cadherin (CDH1) and p53 rather than SMAD4 and Caspase-10 germline mutations contribute to genetic predisposition in Portuguese gastric cancer patients
spellingShingle E-Cadherin (CDH1) and p53 rather than SMAD4 and Caspase-10 germline mutations contribute to genetic predisposition in Portuguese gastric cancer patients
Oliveira, Carla
E-cadherin germline mutations
Familial gastric cancer
Hereditary diffuse gastric cancer
p53 germline mutations
Li-Fraumeni syndrome
SMAD4 mutations
Caspase-10 mutations
title_short E-Cadherin (CDH1) and p53 rather than SMAD4 and Caspase-10 germline mutations contribute to genetic predisposition in Portuguese gastric cancer patients
title_full E-Cadherin (CDH1) and p53 rather than SMAD4 and Caspase-10 germline mutations contribute to genetic predisposition in Portuguese gastric cancer patients
title_fullStr E-Cadherin (CDH1) and p53 rather than SMAD4 and Caspase-10 germline mutations contribute to genetic predisposition in Portuguese gastric cancer patients
title_full_unstemmed E-Cadherin (CDH1) and p53 rather than SMAD4 and Caspase-10 germline mutations contribute to genetic predisposition in Portuguese gastric cancer patients
title_sort E-Cadherin (CDH1) and p53 rather than SMAD4 and Caspase-10 germline mutations contribute to genetic predisposition in Portuguese gastric cancer patients
author Oliveira, Carla
author_facet Oliveira, Carla
Ferreira, Paulo
Nabais, Sérgio
Campos, Luísa
Ferreira, Ana
Cirnes, Luís
Alves, Catarina Castro
Veiga, Isabel
Fragoso, Maria
Regateiro, Fernando
Dias, Luís Moreira
Moreira, Herculano
Suriano, Gianpaolo
Machado, José Carlos
Lopes, Carlos
Castedo, Sérgio
Carneiro, Fátima
Seruca, Raquel
author_role author
author2 Ferreira, Paulo
Nabais, Sérgio
Campos, Luísa
Ferreira, Ana
Cirnes, Luís
Alves, Catarina Castro
Veiga, Isabel
Fragoso, Maria
Regateiro, Fernando
Dias, Luís Moreira
Moreira, Herculano
Suriano, Gianpaolo
Machado, José Carlos
Lopes, Carlos
Castedo, Sérgio
Carneiro, Fátima
Seruca, Raquel
author2_role author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Oliveira, Carla
Ferreira, Paulo
Nabais, Sérgio
Campos, Luísa
Ferreira, Ana
Cirnes, Luís
Alves, Catarina Castro
Veiga, Isabel
Fragoso, Maria
Regateiro, Fernando
Dias, Luís Moreira
Moreira, Herculano
Suriano, Gianpaolo
Machado, José Carlos
Lopes, Carlos
Castedo, Sérgio
Carneiro, Fátima
Seruca, Raquel
dc.subject.por.fl_str_mv E-cadherin germline mutations
Familial gastric cancer
Hereditary diffuse gastric cancer
p53 germline mutations
Li-Fraumeni syndrome
SMAD4 mutations
Caspase-10 mutations
topic E-cadherin germline mutations
Familial gastric cancer
Hereditary diffuse gastric cancer
p53 germline mutations
Li-Fraumeni syndrome
SMAD4 mutations
Caspase-10 mutations
description Approximately 30% of all hereditary diffuse gastric cancer (HDGC) families carry CDH1 germline mutations. The other two thirds remain genetically unexplained and are probably caused by alterations in other genes. Using polymerase chain reaction (PCR)/single-strand conformation polymorphism (SSCP)/sequencing, we screened 32 Portuguese families with a history of gastric cancer and 23 patients with early onset gastric cancer for CDH1 germline mutations. In probands negative for CDH1 mutations, we screened genes involved in hereditary cancer syndromes in which gastric cancer may be one of the component tumours, namely p53 (Li-Fraumeni Syndrome) and hMLH1 and hMSH2 (HNPCC). We also screened in these patients for mutations in Caspase-10, a gene inactivated in sporadic gastric cancer, and SMAD4, a gene whose inactivation in mice is associated with signet-ring cell carcinoma of the stomach. One of the families fulfilling the HDGC criteria harboured a CDH1 germline mutation, and one of the families with incomplete criteria harboured a p53 germline mutation. No mutations were identified in hMLH1 and hMSH2, and only sequence variants were found in SMAD4 and Caspase-10. The present work reports for the first time CDH1 germline mutations in Portuguese gastric cancer families, and highlights the need for p53 mutation screening in families lacking CDH1 germline mutations, in a country with one of the highest incidences of gastric cancer in the world. No evidence was found for a role of germline mutations in SMAD4 and Caspase-10 in families lacking CDH1 mutations.
publishDate 2004
dc.date.none.fl_str_mv 2004
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
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dc.identifier.uri.fl_str_mv https://hdl.handle.net/10316/4780
https://hdl.handle.net/10316/4780
url https://hdl.handle.net/10316/4780
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv European Journal of Cancer. 40:12 (2004) 1897-1903
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dc.format.none.fl_str_mv aplication/PDF
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