DNA mismatch repair gene methylation in gastric cancer in individuals from northern Brazil

Detalhes bibliográficos
Autor(a) principal: Lima, Eleonidas Moura
Data de Publicação: 2008
Outros Autores: Leal, Mariana Ferreira [UNIFESP], Smith, Marilia de Arruda Cardoso [UNIFESP], Burbano, Rommel Rodríguez [UNIFESP], Assumpcao, Paulo Pimentel [UNIFESP], Bello, Maria Jose, Rey, Juan Antonio, Lima, Francinaldo Ferreira de, Casartelli, Cacilda
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNIFESP
Texto Completo: http://www.scielo.org.ar/scielo.php?script=sci_arttext&pid=S0327-95452008000300004&lng=en&nrm=iso&tlng=en
http://repositorio.unifesp.br/handle/11600/42783
Resumo: Gastric cancer is one of the most common malignancies. DNA methylation is implicated in DNA mismatch repair genes deficiency. In the present study, we evaluated the methylation status of MLH1, MSH2, MSH6 and PMS2 in 20 diffuse- and 26 intestinal-type gastric cancer samples and 20 normal gastric mucosal of gastric cancer patients from Northern Brazil. We found that none of the nonneoplastic samples showed methylation of any gene promoter and 50% of gastric, cancer samples showed at least one methylated gene promoter. Methylation frequencies of MLH1, MSH2, MSH6 and PMS2 promoter were 21.74%, 17.39%, 0% and 28.26% respectively in gastric cancer samples. MLH1 and PMS2 methylation were associated with neoplastic samples compared to nonneoplastic ones. PMS2:? methylation was associated with diffuse- and intestinal-type cancer compared with normal controls. Intestinal-type cancer showed significant association with MLH1 methylation. Diffuse-type cancer was significantly associated with MSH2 methylation. Our findings show differential gene methylation in tumoral tissue, which allows us to conclude that methylation is associated with gastric carcinogenesis. Methylation of mismatch repair genes was associated with gastric carcinogenesis and may be a helpful tool for diagnosis, prognosis and therapies. However, MSH6 does not seem to be regulated by methylation in our samples.
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spelling DNA mismatch repair gene methylation in gastric cancer in individuals from northern Brazilgastric cancerMLH1MSH2MSH6PMS2Gastric cancer is one of the most common malignancies. DNA methylation is implicated in DNA mismatch repair genes deficiency. In the present study, we evaluated the methylation status of MLH1, MSH2, MSH6 and PMS2 in 20 diffuse- and 26 intestinal-type gastric cancer samples and 20 normal gastric mucosal of gastric cancer patients from Northern Brazil. We found that none of the nonneoplastic samples showed methylation of any gene promoter and 50% of gastric, cancer samples showed at least one methylated gene promoter. Methylation frequencies of MLH1, MSH2, MSH6 and PMS2 promoter were 21.74%, 17.39%, 0% and 28.26% respectively in gastric cancer samples. MLH1 and PMS2 methylation were associated with neoplastic samples compared to nonneoplastic ones. PMS2:? methylation was associated with diffuse- and intestinal-type cancer compared with normal controls. Intestinal-type cancer showed significant association with MLH1 methylation. Diffuse-type cancer was significantly associated with MSH2 methylation. Our findings show differential gene methylation in tumoral tissue, which allows us to conclude that methylation is associated with gastric carcinogenesis. Methylation of mismatch repair genes was associated with gastric carcinogenesis and may be a helpful tool for diagnosis, prognosis and therapies. However, MSH6 does not seem to be regulated by methylation in our samples.Univ Fed Piaui, Colegiado Biomed, Parnaiba, PI, BrazilUniv Sao Paulo, Fac Med Ribeirao Preto, Dept Genet, Ribeirao Preto, BrazilEscola Paulista Med, Dept Morfol, BR-04023 Sao Paulo, BrazilFed Univ Para, Inst Ciencias Biol, BR-66059 Belem, Para, BrazilHosp Joao Barros Barreto, Serv Cirurgia, Belem, Para, BrazilInst Invest Biomed, Madri, SpainFed Univ Para, Colegiado Ciencias Biol, Altamira, BrazilEscola Paulista Med, Dept Morfol, BR-04023 Sao Paulo, BrazilWeb of ScienceFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)FAEPACoordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Financiadora de Estudos a ProjetosFinanciadora de Estudos a Projetos: FINEP/CT-INFRA 0927-03Inst Histol Embriol-conicetUniv Fed PiauiUniversidade de São Paulo (USP)Universidade Federal de São Paulo (UNIFESP)Fed Univ ParaHosp Joao Barros BarretoInst Invest BiomedLima, Eleonidas MouraLeal, Mariana Ferreira [UNIFESP]Smith, Marilia de Arruda Cardoso [UNIFESP]Burbano, Rommel Rodríguez [UNIFESP]Assumpcao, Paulo Pimentel [UNIFESP]Bello, Maria JoseRey, Juan AntonioLima, Francinaldo Ferreira deCasartelli, Cacilda2018-06-15T14:00:20Z2018-06-15T14:00:20Z2008-12-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion237-243http://www.scielo.org.ar/scielo.php?script=sci_arttext&pid=S0327-95452008000300004&lng=en&nrm=iso&tlng=enBiocell. Mendoza: Inst Histol Embriol-conicet, v. 32, n. 3, p. 237-243, 2008.S0327-95452008000300004.pdf0327-9545S0327-95452008000300004http://repositorio.unifesp.br/handle/11600/42783WOS:000262866400004engBiocellinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2024-05-02T13:59:18Zoai:repositorio.unifesp.br/:11600/42783Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-05-02T13:59:18Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.none.fl_str_mv DNA mismatch repair gene methylation in gastric cancer in individuals from northern Brazil
title DNA mismatch repair gene methylation in gastric cancer in individuals from northern Brazil
spellingShingle DNA mismatch repair gene methylation in gastric cancer in individuals from northern Brazil
Lima, Eleonidas Moura
gastric cancer
MLH1
MSH2
MSH6
PMS2
title_short DNA mismatch repair gene methylation in gastric cancer in individuals from northern Brazil
title_full DNA mismatch repair gene methylation in gastric cancer in individuals from northern Brazil
title_fullStr DNA mismatch repair gene methylation in gastric cancer in individuals from northern Brazil
title_full_unstemmed DNA mismatch repair gene methylation in gastric cancer in individuals from northern Brazil
title_sort DNA mismatch repair gene methylation in gastric cancer in individuals from northern Brazil
author Lima, Eleonidas Moura
author_facet Lima, Eleonidas Moura
Leal, Mariana Ferreira [UNIFESP]
Smith, Marilia de Arruda Cardoso [UNIFESP]
Burbano, Rommel Rodríguez [UNIFESP]
Assumpcao, Paulo Pimentel [UNIFESP]
Bello, Maria Jose
Rey, Juan Antonio
Lima, Francinaldo Ferreira de
Casartelli, Cacilda
author_role author
author2 Leal, Mariana Ferreira [UNIFESP]
Smith, Marilia de Arruda Cardoso [UNIFESP]
Burbano, Rommel Rodríguez [UNIFESP]
Assumpcao, Paulo Pimentel [UNIFESP]
Bello, Maria Jose
Rey, Juan Antonio
Lima, Francinaldo Ferreira de
Casartelli, Cacilda
author2_role author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Univ Fed Piaui
Universidade de São Paulo (USP)
Universidade Federal de São Paulo (UNIFESP)
Fed Univ Para
Hosp Joao Barros Barreto
Inst Invest Biomed
dc.contributor.author.fl_str_mv Lima, Eleonidas Moura
Leal, Mariana Ferreira [UNIFESP]
Smith, Marilia de Arruda Cardoso [UNIFESP]
Burbano, Rommel Rodríguez [UNIFESP]
Assumpcao, Paulo Pimentel [UNIFESP]
Bello, Maria Jose
Rey, Juan Antonio
Lima, Francinaldo Ferreira de
Casartelli, Cacilda
dc.subject.por.fl_str_mv gastric cancer
MLH1
MSH2
MSH6
PMS2
topic gastric cancer
MLH1
MSH2
MSH6
PMS2
description Gastric cancer is one of the most common malignancies. DNA methylation is implicated in DNA mismatch repair genes deficiency. In the present study, we evaluated the methylation status of MLH1, MSH2, MSH6 and PMS2 in 20 diffuse- and 26 intestinal-type gastric cancer samples and 20 normal gastric mucosal of gastric cancer patients from Northern Brazil. We found that none of the nonneoplastic samples showed methylation of any gene promoter and 50% of gastric, cancer samples showed at least one methylated gene promoter. Methylation frequencies of MLH1, MSH2, MSH6 and PMS2 promoter were 21.74%, 17.39%, 0% and 28.26% respectively in gastric cancer samples. MLH1 and PMS2 methylation were associated with neoplastic samples compared to nonneoplastic ones. PMS2:? methylation was associated with diffuse- and intestinal-type cancer compared with normal controls. Intestinal-type cancer showed significant association with MLH1 methylation. Diffuse-type cancer was significantly associated with MSH2 methylation. Our findings show differential gene methylation in tumoral tissue, which allows us to conclude that methylation is associated with gastric carcinogenesis. Methylation of mismatch repair genes was associated with gastric carcinogenesis and may be a helpful tool for diagnosis, prognosis and therapies. However, MSH6 does not seem to be regulated by methylation in our samples.
publishDate 2008
dc.date.none.fl_str_mv 2008-12-01
2018-06-15T14:00:20Z
2018-06-15T14:00:20Z
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://www.scielo.org.ar/scielo.php?script=sci_arttext&pid=S0327-95452008000300004&lng=en&nrm=iso&tlng=en
Biocell. Mendoza: Inst Histol Embriol-conicet, v. 32, n. 3, p. 237-243, 2008.
S0327-95452008000300004.pdf
0327-9545
S0327-95452008000300004
http://repositorio.unifesp.br/handle/11600/42783
WOS:000262866400004
url http://www.scielo.org.ar/scielo.php?script=sci_arttext&pid=S0327-95452008000300004&lng=en&nrm=iso&tlng=en
http://repositorio.unifesp.br/handle/11600/42783
identifier_str_mv Biocell. Mendoza: Inst Histol Embriol-conicet, v. 32, n. 3, p. 237-243, 2008.
S0327-95452008000300004.pdf
0327-9545
S0327-95452008000300004
WOS:000262866400004
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Biocell
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 237-243
dc.publisher.none.fl_str_mv Inst Histol Embriol-conicet
publisher.none.fl_str_mv Inst Histol Embriol-conicet
dc.source.none.fl_str_mv reponame:Repositório Institucional da UNIFESP
instname:Universidade Federal de São Paulo (UNIFESP)
instacron:UNIFESP
instname_str Universidade Federal de São Paulo (UNIFESP)
instacron_str UNIFESP
institution UNIFESP
reponame_str Repositório Institucional da UNIFESP
collection Repositório Institucional da UNIFESP
repository.name.fl_str_mv Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)
repository.mail.fl_str_mv biblioteca.csp@unifesp.br
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