DNA mismatch repair gene methylation in gastric cancer in individuals from northern Brazil
Autor(a) principal: | |
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Data de Publicação: | 2008 |
Outros Autores: | , , , , , , , |
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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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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1814268442662928384 |