CDHI promoter hypermethylation and E-cadherin protein expression in infiltrating breast cancer

Detalhes bibliográficos
Autor(a) principal: Caldeira, Jose Roberto F.
Data de Publicação: 2006
Outros Autores: Prando, Erika C., Quevedo, Francisco C., Moraes Neto, Francisco A., Rainho, Claudia A., Rogatto, Silvia Regina [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1186/1471-2407-6-48
http://hdl.handle.net/11449/13437
Resumo: Background: the E-cadherin gene (CDH1) maps, at chromosome 16q22.1, a region often associated with loss of heterozygosity (LOH) in human breast cancer. LOH at this site is thought to lead to loss of function of this tumor suppressor gene and was correlated with decreased disease-free survival, poor prognosis, and metastasis. Differential CpG island methylation in the promoter region of the CDH1 gene might be an alternative way for the loss of expression and function of E-cadherin, leading to loss of tissue integrity, an essential step in tumor progression.Methods: the aim of our study was to assess, by Methylation-Specific Polymerase Chain Reaction (MSP), the methylation pattern of the CDH1 gene and its possible correlation with the expression of E-cadherin and other standard immunohistochemical parameters (Her-2, ER, PgR, p53, and K-67) in a series of 79 primary breast cancers ( 71 infiltrating ductal, 5 infiltrating lobular, 1 metaplastic, 1 apocrine, and 1 papillary carcinoma).Results: CDH1 hypermethylation was observed in 72% of the cases including 52/71 ductal, 4/5 lobular carcinomas and 1 apocrine carcinoma. Reduced levels of E-cadherin protein were observed in 85% of our samples. Although not statistically significant, the levels of E-cadherin expression tended to diminish with the CDH1 promoter region methylation. In the group of 71 ductal cancinomas, most of the cases of showing CDH1 hypermethylation also presented reduced levels of expression of ER and PgR proteins, and a possible association was observed between CDH1 methylation and ER expression ( p = 0.0301, Fisher's exact test). However, this finding was not considered significant after Bonferroni correction of p-value.Conclusion: Our preliminary findings suggested that abnormal CDH1 methylation occurs in high frequencies in infiltrating breast cancers associated with a decrease in E-cadherin expression in a subgroup of cases characterized by loss of expression of other important genes to the mammary carcinogenesis process, probably due to the disruption of the mechanism of maintenance of DNA methylation in tumoral cells.
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spelling CDHI promoter hypermethylation and E-cadherin protein expression in infiltrating breast cancerBackground: the E-cadherin gene (CDH1) maps, at chromosome 16q22.1, a region often associated with loss of heterozygosity (LOH) in human breast cancer. LOH at this site is thought to lead to loss of function of this tumor suppressor gene and was correlated with decreased disease-free survival, poor prognosis, and metastasis. Differential CpG island methylation in the promoter region of the CDH1 gene might be an alternative way for the loss of expression and function of E-cadherin, leading to loss of tissue integrity, an essential step in tumor progression.Methods: the aim of our study was to assess, by Methylation-Specific Polymerase Chain Reaction (MSP), the methylation pattern of the CDH1 gene and its possible correlation with the expression of E-cadherin and other standard immunohistochemical parameters (Her-2, ER, PgR, p53, and K-67) in a series of 79 primary breast cancers ( 71 infiltrating ductal, 5 infiltrating lobular, 1 metaplastic, 1 apocrine, and 1 papillary carcinoma).Results: CDH1 hypermethylation was observed in 72% of the cases including 52/71 ductal, 4/5 lobular carcinomas and 1 apocrine carcinoma. Reduced levels of E-cadherin protein were observed in 85% of our samples. Although not statistically significant, the levels of E-cadherin expression tended to diminish with the CDH1 promoter region methylation. In the group of 71 ductal cancinomas, most of the cases of showing CDH1 hypermethylation also presented reduced levels of expression of ER and PgR proteins, and a possible association was observed between CDH1 methylation and ER expression ( p = 0.0301, Fisher's exact test). However, this finding was not considered significant after Bonferroni correction of p-value.Conclusion: Our preliminary findings suggested that abnormal CDH1 methylation occurs in high frequencies in infiltrating breast cancers associated with a decrease in E-cadherin expression in a subgroup of cases characterized by loss of expression of other important genes to the mammary carcinogenesis process, probably due to the disruption of the mechanism of maintenance of DNA methylation in tumoral cells.São Paulo State Univ, Fac Med, Dept Urol, NeoGene Lab, BR-18618000 São Paulo, BrazilAmaral Carvalho Hosp, Dept Senol, São Paulo, BrazilSão Paulo State Univ, Inst Biosci, Dept Genet, São Paulo, BrazilAmaral Carvalho Hosp, Dept Pathol, São Paulo, BrazilSão Paulo State Univ, Fac Med, Dept Urol, NeoGene Lab, BR-18618000 São Paulo, BrazilSão Paulo State Univ, Inst Biosci, Dept Genet, São Paulo, BrazilBiomed Central Ltd.Universidade Estadual Paulista (Unesp)Amaral Carvalho HospCaldeira, Jose Roberto F.Prando, Erika C.Quevedo, Francisco C.Moraes Neto, Francisco A.Rainho, Claudia A.Rogatto, Silvia Regina [UNESP]2014-05-20T13:38:45Z2014-05-20T13:38:45Z2006-03-02info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article9application/pdfhttp://dx.doi.org/10.1186/1471-2407-6-48Bmc Cancer. London: Biomed Central Ltd., v. 6, 9 p., 2006.1471-2407http://hdl.handle.net/11449/1343710.1186/1471-2407-6-48WOS:000239316600001WOS000239316600001.pdf225998654626557988148235451595040000-0002-0285-1162Web of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengBMC Cancer3.2881,464info:eu-repo/semantics/openAccess2024-09-03T14:30:11Zoai:repositorio.unesp.br:11449/13437Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestrepositoriounesp@unesp.bropendoar:29462024-09-03T14:30:11Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv CDHI promoter hypermethylation and E-cadherin protein expression in infiltrating breast cancer
title CDHI promoter hypermethylation and E-cadherin protein expression in infiltrating breast cancer
spellingShingle CDHI promoter hypermethylation and E-cadherin protein expression in infiltrating breast cancer
Caldeira, Jose Roberto F.
title_short CDHI promoter hypermethylation and E-cadherin protein expression in infiltrating breast cancer
title_full CDHI promoter hypermethylation and E-cadherin protein expression in infiltrating breast cancer
title_fullStr CDHI promoter hypermethylation and E-cadherin protein expression in infiltrating breast cancer
title_full_unstemmed CDHI promoter hypermethylation and E-cadherin protein expression in infiltrating breast cancer
title_sort CDHI promoter hypermethylation and E-cadherin protein expression in infiltrating breast cancer
author Caldeira, Jose Roberto F.
author_facet Caldeira, Jose Roberto F.
Prando, Erika C.
Quevedo, Francisco C.
Moraes Neto, Francisco A.
Rainho, Claudia A.
Rogatto, Silvia Regina [UNESP]
author_role author
author2 Prando, Erika C.
Quevedo, Francisco C.
Moraes Neto, Francisco A.
Rainho, Claudia A.
Rogatto, Silvia Regina [UNESP]
author2_role author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (Unesp)
Amaral Carvalho Hosp
dc.contributor.author.fl_str_mv Caldeira, Jose Roberto F.
Prando, Erika C.
Quevedo, Francisco C.
Moraes Neto, Francisco A.
Rainho, Claudia A.
Rogatto, Silvia Regina [UNESP]
description Background: the E-cadherin gene (CDH1) maps, at chromosome 16q22.1, a region often associated with loss of heterozygosity (LOH) in human breast cancer. LOH at this site is thought to lead to loss of function of this tumor suppressor gene and was correlated with decreased disease-free survival, poor prognosis, and metastasis. Differential CpG island methylation in the promoter region of the CDH1 gene might be an alternative way for the loss of expression and function of E-cadherin, leading to loss of tissue integrity, an essential step in tumor progression.Methods: the aim of our study was to assess, by Methylation-Specific Polymerase Chain Reaction (MSP), the methylation pattern of the CDH1 gene and its possible correlation with the expression of E-cadherin and other standard immunohistochemical parameters (Her-2, ER, PgR, p53, and K-67) in a series of 79 primary breast cancers ( 71 infiltrating ductal, 5 infiltrating lobular, 1 metaplastic, 1 apocrine, and 1 papillary carcinoma).Results: CDH1 hypermethylation was observed in 72% of the cases including 52/71 ductal, 4/5 lobular carcinomas and 1 apocrine carcinoma. Reduced levels of E-cadherin protein were observed in 85% of our samples. Although not statistically significant, the levels of E-cadherin expression tended to diminish with the CDH1 promoter region methylation. In the group of 71 ductal cancinomas, most of the cases of showing CDH1 hypermethylation also presented reduced levels of expression of ER and PgR proteins, and a possible association was observed between CDH1 methylation and ER expression ( p = 0.0301, Fisher's exact test). However, this finding was not considered significant after Bonferroni correction of p-value.Conclusion: Our preliminary findings suggested that abnormal CDH1 methylation occurs in high frequencies in infiltrating breast cancers associated with a decrease in E-cadherin expression in a subgroup of cases characterized by loss of expression of other important genes to the mammary carcinogenesis process, probably due to the disruption of the mechanism of maintenance of DNA methylation in tumoral cells.
publishDate 2006
dc.date.none.fl_str_mv 2006-03-02
2014-05-20T13:38:45Z
2014-05-20T13:38:45Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1186/1471-2407-6-48
Bmc Cancer. London: Biomed Central Ltd., v. 6, 9 p., 2006.
1471-2407
http://hdl.handle.net/11449/13437
10.1186/1471-2407-6-48
WOS:000239316600001
WOS000239316600001.pdf
2259986546265579
8814823545159504
0000-0002-0285-1162
url http://dx.doi.org/10.1186/1471-2407-6-48
http://hdl.handle.net/11449/13437
identifier_str_mv Bmc Cancer. London: Biomed Central Ltd., v. 6, 9 p., 2006.
1471-2407
10.1186/1471-2407-6-48
WOS:000239316600001
WOS000239316600001.pdf
2259986546265579
8814823545159504
0000-0002-0285-1162
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv BMC Cancer
3.288
1,464
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 9
application/pdf
dc.publisher.none.fl_str_mv Biomed Central Ltd.
publisher.none.fl_str_mv Biomed Central Ltd.
dc.source.none.fl_str_mv Web of Science
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
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institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv repositoriounesp@unesp.br
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