Prevalence of <it>BRCA1 </it>and <it>BRCA2 </it>mutations in unselected breast cancer patients from Greece

<p>Abstract</p> <p>Background</p> <p>Inheritance of a mutation in either <it>BRCA1 </it>or <it>BRCA2 </it>accounts for approximately 5% of all breast cancer cases, but varies by country. Investigations into the contribution of <it>BRCA <...

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Main Authors: Koumpis Chrissovaladis, Dimitrakakis Constantine, Antsaklis Aris, Royer Robert, Zhang Shiyu, Narod Steven A, Kotsopoulos Joanne
Format: Article
Language:English
Published: BMC 2011-11-01
Series:Hereditary Cancer in Clinical Practice
Online Access:http://www.hccpjournal.com/content/9/1/10
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author Koumpis Chrissovaladis
Dimitrakakis Constantine
Antsaklis Aris
Royer Robert
Zhang Shiyu
Narod Steven A
Kotsopoulos Joanne
author_facet Koumpis Chrissovaladis
Dimitrakakis Constantine
Antsaklis Aris
Royer Robert
Zhang Shiyu
Narod Steven A
Kotsopoulos Joanne
author_sort Koumpis Chrissovaladis
collection DOAJ
description <p>Abstract</p> <p>Background</p> <p>Inheritance of a mutation in either <it>BRCA1 </it>or <it>BRCA2 </it>accounts for approximately 5% of all breast cancer cases, but varies by country. Investigations into the contribution of <it>BRCA </it>mutations to breast cancer incidence in Greece have been, for the most part, limited by small sample sizes and by the use of cases selected for their family history of cancer. The aim of the current study was to estimate <it>BRCA </it>mutation frequencies in breast cancer patients unselected for family history.</p> <p>Methods</p> <p>To do so, we enrolled 127 unselected women with breast cancer from the Alexandra Hospital in Athens, Greece, a large public hospital in the city. Mutations in <it>BRCA1 </it>and <it>BRCA2 </it>were detected using a combination of techniques and were confirmed by direct sequencing. Two large genomic deletions were sought using mutation-specific assays. A detailed family history of cancer was obtained from each patient.</p> <p>Results</p> <p>We were able to successfully complete testing on samples from 127 women. Among these, six mutations were identified (four in <it>BRCA1 </it>and two in <it>BRCA2</it>) representing 4.7% of the total or 9.5% of cases diagnosed before age forty. None of the mutation carriers had a family history of breast or ovarian cancer. Three of the four <it>BRCA1 </it>mutations were in exon 20: two were a G5331A mutation and the third was a 3.2 kb deletion. The fourth <it>BRCA1 </it>mutation was the 3819delGTAAA in exon 11. The two <it>BRCA2 </it>mutations were in exon 11 (3782del10 and 4512insT).</p> <p>Conclusions</p> <p>The G5331A mutation in <it>BRCA1 </it>appears to be a founder mutation in the Greek population.</p>
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spelling doaj.art-6ea3cd94b2de431483f7da620d2a159c2022-12-21T19:03:50ZengBMCHereditary Cancer in Clinical Practice1897-42872011-11-01911010.1186/1897-4287-9-10Prevalence of <it>BRCA1 </it>and <it>BRCA2 </it>mutations in unselected breast cancer patients from GreeceKoumpis ChrissovaladisDimitrakakis ConstantineAntsaklis ArisRoyer RobertZhang ShiyuNarod Steven AKotsopoulos Joanne<p>Abstract</p> <p>Background</p> <p>Inheritance of a mutation in either <it>BRCA1 </it>or <it>BRCA2 </it>accounts for approximately 5% of all breast cancer cases, but varies by country. Investigations into the contribution of <it>BRCA </it>mutations to breast cancer incidence in Greece have been, for the most part, limited by small sample sizes and by the use of cases selected for their family history of cancer. The aim of the current study was to estimate <it>BRCA </it>mutation frequencies in breast cancer patients unselected for family history.</p> <p>Methods</p> <p>To do so, we enrolled 127 unselected women with breast cancer from the Alexandra Hospital in Athens, Greece, a large public hospital in the city. Mutations in <it>BRCA1 </it>and <it>BRCA2 </it>were detected using a combination of techniques and were confirmed by direct sequencing. Two large genomic deletions were sought using mutation-specific assays. A detailed family history of cancer was obtained from each patient.</p> <p>Results</p> <p>We were able to successfully complete testing on samples from 127 women. Among these, six mutations were identified (four in <it>BRCA1 </it>and two in <it>BRCA2</it>) representing 4.7% of the total or 9.5% of cases diagnosed before age forty. None of the mutation carriers had a family history of breast or ovarian cancer. Three of the four <it>BRCA1 </it>mutations were in exon 20: two were a G5331A mutation and the third was a 3.2 kb deletion. The fourth <it>BRCA1 </it>mutation was the 3819delGTAAA in exon 11. The two <it>BRCA2 </it>mutations were in exon 11 (3782del10 and 4512insT).</p> <p>Conclusions</p> <p>The G5331A mutation in <it>BRCA1 </it>appears to be a founder mutation in the Greek population.</p>http://www.hccpjournal.com/content/9/1/10
spellingShingle Koumpis Chrissovaladis
Dimitrakakis Constantine
Antsaklis Aris
Royer Robert
Zhang Shiyu
Narod Steven A
Kotsopoulos Joanne
Prevalence of <it>BRCA1 </it>and <it>BRCA2 </it>mutations in unselected breast cancer patients from Greece
Hereditary Cancer in Clinical Practice
title Prevalence of <it>BRCA1 </it>and <it>BRCA2 </it>mutations in unselected breast cancer patients from Greece
title_full Prevalence of <it>BRCA1 </it>and <it>BRCA2 </it>mutations in unselected breast cancer patients from Greece
title_fullStr Prevalence of <it>BRCA1 </it>and <it>BRCA2 </it>mutations in unselected breast cancer patients from Greece
title_full_unstemmed Prevalence of <it>BRCA1 </it>and <it>BRCA2 </it>mutations in unselected breast cancer patients from Greece
title_short Prevalence of <it>BRCA1 </it>and <it>BRCA2 </it>mutations in unselected breast cancer patients from Greece
title_sort prevalence of it brca1 it and it brca2 it mutations in unselected breast cancer patients from greece
url http://www.hccpjournal.com/content/9/1/10
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AT royerrobert prevalenceofitbrca1itanditbrca2itmutationsinunselectedbreastcancerpatientsfromgreece
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