Prevalence of 185delAG and 5382insC mutations in BRCA1, and 6174delT in BRCA2 in women of Ashkenazi Jewish origin in southern Brazil
Autor(a) principal: | |
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Data de Publicação: | 2012 |
Outros Autores: | , , , , , |
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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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 InstitucionalPUBhttps://lume.ufrgs.br/oai/requestlume@ufrgs.bropendoar: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 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/other |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://hdl.handle.net/10183/147456 |
dc.identifier.issn.pt_BR.fl_str_mv |
1415-4757 |
dc.identifier.nrb.pt_BR.fl_str_mv |
000996708 |
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http://hdl.handle.net/10183/147456 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
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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info:eu-repo/semantics/openAccess |
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openAccess |
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