DNA repair gene <it>ERCC2 </it>polymorphisms and associations with breast and ovarian cancer risk

<p>Abstract</p> <p>Breast and ovarian cancers increased in the last decades. Except rare cases with a genetic predisposition and high penetrance, these pathologies are viewed as a polygenic disease. In this concept, association studies look for genetic variations such as polymorphi...

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Main Authors: Rabiau Nadège, Chamoux Alain, Fontana Luc, Delort Laetitia, Bosviel Rémy, Bernard-Gallon Dominique, Kwiatkowski Fabrice, Chalabi Nasséra, Satih Samir, Bignon Yves-Jean
Format: Article
Language:English
Published: BMC 2008-05-01
Series:Molecular Cancer
Online Access:http://www.molecular-cancer.com/content/7/1/36
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spelling doaj-60b912979da943ecbc1406a1f202c43a2020-11-24T21:41:42ZengBMCMolecular Cancer1476-45982008-05-01713610.1186/1476-4598-7-36DNA repair gene <it>ERCC2 </it>polymorphisms and associations with breast and ovarian cancer riskRabiau NadègeChamoux AlainFontana LucDelort LaetitiaBosviel RémyBernard-Gallon DominiqueKwiatkowski FabriceChalabi NasséraSatih SamirBignon Yves-Jean<p>Abstract</p> <p>Breast and ovarian cancers increased in the last decades. Except rare cases with a genetic predisposition and high penetrance, these pathologies are viewed as a polygenic disease. In this concept, association studies look for genetic variations such as polymorphisms in low penetrance genes, <it>i.e</it>. genes in interaction with environmental factors. DNA repair systems that protect the genome from deleterious endogenous and exogenous damages have been shown to have significantly reduced. In particular, enzymes of the nucleotide excision repair pathway are suspected to be implicated in cancer. In this study, 2 functional polymorphisms in a DNA repair gene <it>ERCC2 </it>were analyzed. The population included 911 breast cancer cases, 51 ovarian cancer cases and 1000 controls. The genotyping of 2 SNP (Single Nucleotide Polymorphism) was carried out on the population with the MGB (Minor Groove Binder) probe technique which consists of the use of the allelic discrimination with the Taqman<sup>® </sup>method. This study enabled us to show an increase in risk of breast cancer with no oral contraceptive users and with women exhibiting a waist-to-hip ratio (WHR) > 0.85 for Asn homozygous for <it>ERCC2 312</it>.</p> http://www.molecular-cancer.com/content/7/1/36
collection DOAJ
language English
format Article
sources DOAJ
author Rabiau Nadège
Chamoux Alain
Fontana Luc
Delort Laetitia
Bosviel Rémy
Bernard-Gallon Dominique
Kwiatkowski Fabrice
Chalabi Nasséra
Satih Samir
Bignon Yves-Jean
spellingShingle Rabiau Nadège
Chamoux Alain
Fontana Luc
Delort Laetitia
Bosviel Rémy
Bernard-Gallon Dominique
Kwiatkowski Fabrice
Chalabi Nasséra
Satih Samir
Bignon Yves-Jean
DNA repair gene <it>ERCC2 </it>polymorphisms and associations with breast and ovarian cancer risk
Molecular Cancer
author_facet Rabiau Nadège
Chamoux Alain
Fontana Luc
Delort Laetitia
Bosviel Rémy
Bernard-Gallon Dominique
Kwiatkowski Fabrice
Chalabi Nasséra
Satih Samir
Bignon Yves-Jean
author_sort Rabiau Nadège
title DNA repair gene <it>ERCC2 </it>polymorphisms and associations with breast and ovarian cancer risk
title_short DNA repair gene <it>ERCC2 </it>polymorphisms and associations with breast and ovarian cancer risk
title_full DNA repair gene <it>ERCC2 </it>polymorphisms and associations with breast and ovarian cancer risk
title_fullStr DNA repair gene <it>ERCC2 </it>polymorphisms and associations with breast and ovarian cancer risk
title_full_unstemmed DNA repair gene <it>ERCC2 </it>polymorphisms and associations with breast and ovarian cancer risk
title_sort dna repair gene <it>ercc2 </it>polymorphisms and associations with breast and ovarian cancer risk
publisher BMC
series Molecular Cancer
issn 1476-4598
publishDate 2008-05-01
description <p>Abstract</p> <p>Breast and ovarian cancers increased in the last decades. Except rare cases with a genetic predisposition and high penetrance, these pathologies are viewed as a polygenic disease. In this concept, association studies look for genetic variations such as polymorphisms in low penetrance genes, <it>i.e</it>. genes in interaction with environmental factors. DNA repair systems that protect the genome from deleterious endogenous and exogenous damages have been shown to have significantly reduced. In particular, enzymes of the nucleotide excision repair pathway are suspected to be implicated in cancer. In this study, 2 functional polymorphisms in a DNA repair gene <it>ERCC2 </it>were analyzed. The population included 911 breast cancer cases, 51 ovarian cancer cases and 1000 controls. The genotyping of 2 SNP (Single Nucleotide Polymorphism) was carried out on the population with the MGB (Minor Groove Binder) probe technique which consists of the use of the allelic discrimination with the Taqman<sup>® </sup>method. This study enabled us to show an increase in risk of breast cancer with no oral contraceptive users and with women exhibiting a waist-to-hip ratio (WHR) > 0.85 for Asn homozygous for <it>ERCC2 312</it>.</p>
url http://www.molecular-cancer.com/content/7/1/36
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