DNA repair genes XRCC1 and XRCC3 polymorphisms and their relationship with the level of micronuclei in breast cancer patients

Breast cancer (BC) is the most prevalent type worldwide, besides being one of the most common causes of death among women. It has been suggested that sporadic BC is most likely caused by low-penetrance genes, including those involved in DNA repair mechanisms. Furthermore, the accumulation of DNA dam...

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Main Authors: Raquel A. Santos, Ana Claudia Teixeira, Monica B. Mayorano, Helio H.A. Carrara, Jurandyr M. Andrade, Catarina S. Takahashi
Format: Article
Language:English
Published: Sociedade Brasileira de Genética 2010-01-01
Series:Genetics and Molecular Biology
Subjects:
Online Access:http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572010000400007
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author Raquel A. Santos
Ana Claudia Teixeira
Monica B. Mayorano
Helio H.A. Carrara
Jurandyr M. Andrade
Catarina S. Takahashi
author_facet Raquel A. Santos
Ana Claudia Teixeira
Monica B. Mayorano
Helio H.A. Carrara
Jurandyr M. Andrade
Catarina S. Takahashi
author_sort Raquel A. Santos
collection DOAJ
description Breast cancer (BC) is the most prevalent type worldwide, besides being one of the most common causes of death among women. It has been suggested that sporadic BC is most likely caused by low-penetrance genes, including those involved in DNA repair mechanisms. Furthermore, the accumulation of DNA damage may contribute to breast carcinogenesis. In the present study, the relationship between two DNA repair genes, viz., XRCC1 (Arg399Gln) and XRCC3 (Thr241Met) polymorphisms, and the levels of chromosome damage detected in 65 untreated BC women and 85 healthy controls, was investigated. Chromosome damage was evaluated through micronucleus assaying, and genotypes determined by PCR-RFLP methodology. The results showed no alteration in the risk of BC and DNA damage brought about by either XRCC1 (Arg399Gln) or XRCC3 (Thr241Met) action in either of the two groups. Nevertheless, on evaluating BC risk in women presenting levels of chromosome damage above the mean, the XRCC3 Thr241Met polymorphism was found to be more frequent in the BC group than in the control, thereby leading to the conclusion that there is a slight association between XRCC3 (241 C/T) genotypes and BC risk in the subgroups with higher levels of chromosome damage.
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spelling doaj.art-b07c6f1b2cc3495c8e9a26583bf1e71f2022-12-21T17:31:50ZengSociedade Brasileira de GenéticaGenetics and Molecular Biology1415-47571678-46852010-01-01334637640DNA repair genes XRCC1 and XRCC3 polymorphisms and their relationship with the level of micronuclei in breast cancer patientsRaquel A. SantosAna Claudia TeixeiraMonica B. MayoranoHelio H.A. CarraraJurandyr M. AndradeCatarina S. TakahashiBreast cancer (BC) is the most prevalent type worldwide, besides being one of the most common causes of death among women. It has been suggested that sporadic BC is most likely caused by low-penetrance genes, including those involved in DNA repair mechanisms. Furthermore, the accumulation of DNA damage may contribute to breast carcinogenesis. In the present study, the relationship between two DNA repair genes, viz., XRCC1 (Arg399Gln) and XRCC3 (Thr241Met) polymorphisms, and the levels of chromosome damage detected in 65 untreated BC women and 85 healthy controls, was investigated. Chromosome damage was evaluated through micronucleus assaying, and genotypes determined by PCR-RFLP methodology. The results showed no alteration in the risk of BC and DNA damage brought about by either XRCC1 (Arg399Gln) or XRCC3 (Thr241Met) action in either of the two groups. Nevertheless, on evaluating BC risk in women presenting levels of chromosome damage above the mean, the XRCC3 Thr241Met polymorphism was found to be more frequent in the BC group than in the control, thereby leading to the conclusion that there is a slight association between XRCC3 (241 C/T) genotypes and BC risk in the subgroups with higher levels of chromosome damage.http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572010000400007DNA repair polymorphismsbreast cancermicronucleus assay
spellingShingle Raquel A. Santos
Ana Claudia Teixeira
Monica B. Mayorano
Helio H.A. Carrara
Jurandyr M. Andrade
Catarina S. Takahashi
DNA repair genes XRCC1 and XRCC3 polymorphisms and their relationship with the level of micronuclei in breast cancer patients
Genetics and Molecular Biology
DNA repair polymorphisms
breast cancer
micronucleus assay
title DNA repair genes XRCC1 and XRCC3 polymorphisms and their relationship with the level of micronuclei in breast cancer patients
title_full DNA repair genes XRCC1 and XRCC3 polymorphisms and their relationship with the level of micronuclei in breast cancer patients
title_fullStr DNA repair genes XRCC1 and XRCC3 polymorphisms and their relationship with the level of micronuclei in breast cancer patients
title_full_unstemmed DNA repair genes XRCC1 and XRCC3 polymorphisms and their relationship with the level of micronuclei in breast cancer patients
title_short DNA repair genes XRCC1 and XRCC3 polymorphisms and their relationship with the level of micronuclei in breast cancer patients
title_sort dna repair genes xrcc1 and xrcc3 polymorphisms and their relationship with the level of micronuclei in breast cancer patients
topic DNA repair polymorphisms
breast cancer
micronucleus assay
url http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572010000400007
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