Prevalence of 185delAG and 5382insC mutations in BRCA1, and 6174delT in BRCA2 in women of Ashkenazi Jewish origin in southern Brazil

Detalhes bibliográficos
Autor(a) principal: Dillenburg, Criste Vignol
Data de Publicação: 2012
Outros Autores: Bandeira, Isabel Cristina, Tubino, Taiana Valente, Rossato, Luciana Grazziotin, Dias, Eleonora Souza, Bittelbrunn, Ana Cristina da Costa, Leistner-Segal, Sandra
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UFRGS
Texto Completo: http://hdl.handle.net/10183/147456
Resumo: Certain mutations in BRCA1 and BRCA2 genes are frequent in the Ashkenazi Jewish population. Several factors contribute to this increased frequency, including consanguineous marriages and an event known as a “bottleneck”, which occurred in the past and caused a drastic reduction in the genetic variability of this population. Several studies were performed over the years in an attempt to elucidate the role of BRCA1 and BRCA2 genes in susceptibility to breast cancer. The aim of this study was to estimate the carrier frequency of certain common mutations in theBRCA1 (185delAG and 5382insC) and BRCA2 (6174delT) genes in an Ashkenazi Jewish population from Porto Alegre, Brazil. Molecular analyses were done by PCR followed by RFLP (ACRS). The carrier frequencies for BRCA1 185delAG and 5382insC were 0.78 and 0 respectively, and 0.4 for theBRCA2 6174deT mutation. These findings are similar to those of some prior studies but differ from others, possibly due to excluding individuals with a personal or family history of cancer. Our sample was drawn from the community group and included individuals with or without a family or personal history of cancer. Furthermore, increased dispersion among Ashkenazi subpopulations may be the result of strong genetic drift and/or admixture. It is therefore necessary to consider the effects of local admixture on the mismatch distributions of various Jewish populations.
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spelling Dillenburg, Criste VignolBandeira, Isabel CristinaTubino, Taiana ValenteRossato, Luciana GrazziotinDias, Eleonora SouzaBittelbrunn, Ana Cristina da CostaLeistner-Segal, Sandra2016-08-20T02:14:31Z20121415-4757http://hdl.handle.net/10183/147456000996708Certain mutations in BRCA1 and BRCA2 genes are frequent in the Ashkenazi Jewish population. Several factors contribute to this increased frequency, including consanguineous marriages and an event known as a “bottleneck”, which occurred in the past and caused a drastic reduction in the genetic variability of this population. Several studies were performed over the years in an attempt to elucidate the role of BRCA1 and BRCA2 genes in susceptibility to breast cancer. The aim of this study was to estimate the carrier frequency of certain common mutations in theBRCA1 (185delAG and 5382insC) and BRCA2 (6174delT) genes in an Ashkenazi Jewish population from Porto Alegre, Brazil. Molecular analyses were done by PCR followed by RFLP (ACRS). The carrier frequencies for BRCA1 185delAG and 5382insC were 0.78 and 0 respectively, and 0.4 for theBRCA2 6174deT mutation. These findings are similar to those of some prior studies but differ from others, possibly due to excluding individuals with a personal or family history of cancer. Our sample was drawn from the community group and included individuals with or without a family or personal history of cancer. Furthermore, increased dispersion among Ashkenazi subpopulations may be the result of strong genetic drift and/or admixture. It is therefore necessary to consider the effects of local admixture on the mismatch distributions of various Jewish populations.application/pdfengGenetics and molecular biology. Ribeirão Preto, SP. Vol. 35, no. 3 (2012), p. 599-602Genes BRCA1Genes BRCA2Neoplasias da mamaMutaçãoFemininoJudeusPorto Alegre (RS)Ashkenazi JewsBreast cancerBRCA1BRCA2MutationPrevalence of 185delAG and 5382insC mutations in BRCA1, and 6174delT in BRCA2 in women of Ashkenazi Jewish origin in southern Brazilinfo:eu-repo/semantics/articleinfo:eu-repo/semantics/otherinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFRGSinstname:Universidade Federal do Rio Grande do Sul (UFRGS)instacron:UFRGSORIGINAL000996708.pdf000996708.pdfTexto completo (inglês)application/pdf447842http://www.lume.ufrgs.br/bitstream/10183/147456/1/000996708.pdf6a5704cde46c14c2ac4b3102cb999871MD51TEXT000996708.pdf.txt000996708.pdf.txtExtracted Texttext/plain15986http://www.lume.ufrgs.br/bitstream/10183/147456/2/000996708.pdf.txt980d9771f700c1951f6c7ba5cc64096aMD52THUMBNAIL000996708.pdf.jpg000996708.pdf.jpgGenerated Thumbnailimage/jpeg1882http://www.lume.ufrgs.br/bitstream/10183/147456/3/000996708.pdf.jpg7ecf9cccbe1f084c37d56f963af55ad5MD5310183/1474562018-10-29 08:37:27.072oai:www.lume.ufrgs.br:10183/147456Repositório de PublicaçõesPUBhttps://lume.ufrgs.br/oai/requestopendoar:2018-10-29T11:37:27Repositório Institucional da UFRGS - Universidade Federal do Rio Grande do Sul (UFRGS)false
dc.title.pt_BR.fl_str_mv Prevalence of 185delAG and 5382insC mutations in BRCA1, and 6174delT in BRCA2 in women of Ashkenazi Jewish origin in southern Brazil
title Prevalence of 185delAG and 5382insC mutations in BRCA1, and 6174delT in BRCA2 in women of Ashkenazi Jewish origin in southern Brazil
spellingShingle Prevalence of 185delAG and 5382insC mutations in BRCA1, and 6174delT in BRCA2 in women of Ashkenazi Jewish origin in southern Brazil
Dillenburg, Criste Vignol
Genes BRCA1
Genes BRCA2
Neoplasias da mama
Mutação
Feminino
Judeus
Porto Alegre (RS)
Ashkenazi Jews
Breast cancer
BRCA1
BRCA2
Mutation
title_short Prevalence of 185delAG and 5382insC mutations in BRCA1, and 6174delT in BRCA2 in women of Ashkenazi Jewish origin in southern Brazil
title_full Prevalence of 185delAG and 5382insC mutations in BRCA1, and 6174delT in BRCA2 in women of Ashkenazi Jewish origin in southern Brazil
title_fullStr Prevalence of 185delAG and 5382insC mutations in BRCA1, and 6174delT in BRCA2 in women of Ashkenazi Jewish origin in southern Brazil
title_full_unstemmed Prevalence of 185delAG and 5382insC mutations in BRCA1, and 6174delT in BRCA2 in women of Ashkenazi Jewish origin in southern Brazil
title_sort Prevalence of 185delAG and 5382insC mutations in BRCA1, and 6174delT in BRCA2 in women of Ashkenazi Jewish origin in southern Brazil
author Dillenburg, Criste Vignol
author_facet Dillenburg, Criste Vignol
Bandeira, Isabel Cristina
Tubino, Taiana Valente
Rossato, Luciana Grazziotin
Dias, Eleonora Souza
Bittelbrunn, Ana Cristina da Costa
Leistner-Segal, Sandra
author_role author
author2 Bandeira, Isabel Cristina
Tubino, Taiana Valente
Rossato, Luciana Grazziotin
Dias, Eleonora Souza
Bittelbrunn, Ana Cristina da Costa
Leistner-Segal, Sandra
author2_role author
author
author
author
author
author
dc.contributor.author.fl_str_mv Dillenburg, Criste Vignol
Bandeira, Isabel Cristina
Tubino, Taiana Valente
Rossato, Luciana Grazziotin
Dias, Eleonora Souza
Bittelbrunn, Ana Cristina da Costa
Leistner-Segal, Sandra
dc.subject.por.fl_str_mv Genes BRCA1
Genes BRCA2
Neoplasias da mama
Mutação
Feminino
Judeus
Porto Alegre (RS)
topic Genes BRCA1
Genes BRCA2
Neoplasias da mama
Mutação
Feminino
Judeus
Porto Alegre (RS)
Ashkenazi Jews
Breast cancer
BRCA1
BRCA2
Mutation
dc.subject.eng.fl_str_mv Ashkenazi Jews
Breast cancer
BRCA1
BRCA2
Mutation
description Certain mutations in BRCA1 and BRCA2 genes are frequent in the Ashkenazi Jewish population. Several factors contribute to this increased frequency, including consanguineous marriages and an event known as a “bottleneck”, which occurred in the past and caused a drastic reduction in the genetic variability of this population. Several studies were performed over the years in an attempt to elucidate the role of BRCA1 and BRCA2 genes in susceptibility to breast cancer. The aim of this study was to estimate the carrier frequency of certain common mutations in theBRCA1 (185delAG and 5382insC) and BRCA2 (6174delT) genes in an Ashkenazi Jewish population from Porto Alegre, Brazil. Molecular analyses were done by PCR followed by RFLP (ACRS). The carrier frequencies for BRCA1 185delAG and 5382insC were 0.78 and 0 respectively, and 0.4 for theBRCA2 6174deT mutation. These findings are similar to those of some prior studies but differ from others, possibly due to excluding individuals with a personal or family history of cancer. Our sample was drawn from the community group and included individuals with or without a family or personal history of cancer. Furthermore, increased dispersion among Ashkenazi subpopulations may be the result of strong genetic drift and/or admixture. It is therefore necessary to consider the effects of local admixture on the mismatch distributions of various Jewish populations.
publishDate 2012
dc.date.issued.fl_str_mv 2012
dc.date.accessioned.fl_str_mv 2016-08-20T02:14:31Z
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dc.relation.ispartof.pt_BR.fl_str_mv Genetics and molecular biology. Ribeirão Preto, SP. Vol. 35, no. 3 (2012), p. 599-602
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