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Determination of CYP2D6 *3, *4, and *10 frequency in women with breast cancer in São Luís, Brazil, and its association with prognostic factors and disease-free survival
The CYP2D6 enzyme is crucial for the metabolism of tamoxifen. The CYP2D6 gene is highly polymorphic, and individuals can be extensive, intermediate, or poor tamoxifen metabolizers. The aim of this study was to determine the frequencies of the CYP2D6 *3, *4, and *10 alleles in women with breast cance...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Associação Brasileira de Divulgação Científica
2014
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4230293/ https://www.ncbi.nlm.nih.gov/pubmed/25296365 http://dx.doi.org/10.1590/1414-431X20143761 |
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author | Martins, D.M.F. Vidal, F.C.B. Souza, R.D.M. Brusaca, S.A. Brito, L.M.O. |
author_facet | Martins, D.M.F. Vidal, F.C.B. Souza, R.D.M. Brusaca, S.A. Brito, L.M.O. |
author_sort | Martins, D.M.F. |
collection | PubMed |
description | The CYP2D6 enzyme is crucial for the metabolism of tamoxifen. The CYP2D6 gene is highly polymorphic, and individuals can be extensive, intermediate, or poor tamoxifen metabolizers. The aim of this study was to determine the frequencies of the CYP2D6 *3, *4, and *10 alleles in women with breast cancer who were treated with tamoxifen and analyze the association of enzyme activity with prognostic factors and disease-free survival. We observed a high frequency of CYP2D6 *10, with an allelic frequency of 0.14 (14.4%). The *3 allele was not present in the studied population, and *4 had an allelic frequency of 0.13 (13.8%). We conclude that patients with reduced CYP2D6 activity did not present worse tumor characteristics or decreased disease-free survival than women with normal enzyme activity, as the difference was not statistically significant. We also observed a high frequency of CYP2D6 *10, which had not been previously described in this specific population. This study is the first in north-northeastern Brazil that aimed to contribute to the knowledge of the Brazilian regional profile for CYP2D6 polymorphisms and their phenotypes. These findings add to the knowledge of the distribution of different polymorphic CYP2D6 alleles and the potential role of CYP2D6 genotyping in clinical practice prior to choosing therapeutic protocols. |
format | Online Article Text |
id | pubmed-4230293 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Associação Brasileira de Divulgação Científica |
record_format | MEDLINE/PubMed |
spelling | pubmed-42302932014-12-02 Determination of CYP2D6 *3, *4, and *10 frequency in women with breast cancer in São Luís, Brazil, and its association with prognostic factors and disease-free survival Martins, D.M.F. Vidal, F.C.B. Souza, R.D.M. Brusaca, S.A. Brito, L.M.O. Braz J Med Biol Res Clinical Investigation The CYP2D6 enzyme is crucial for the metabolism of tamoxifen. The CYP2D6 gene is highly polymorphic, and individuals can be extensive, intermediate, or poor tamoxifen metabolizers. The aim of this study was to determine the frequencies of the CYP2D6 *3, *4, and *10 alleles in women with breast cancer who were treated with tamoxifen and analyze the association of enzyme activity with prognostic factors and disease-free survival. We observed a high frequency of CYP2D6 *10, with an allelic frequency of 0.14 (14.4%). The *3 allele was not present in the studied population, and *4 had an allelic frequency of 0.13 (13.8%). We conclude that patients with reduced CYP2D6 activity did not present worse tumor characteristics or decreased disease-free survival than women with normal enzyme activity, as the difference was not statistically significant. We also observed a high frequency of CYP2D6 *10, which had not been previously described in this specific population. This study is the first in north-northeastern Brazil that aimed to contribute to the knowledge of the Brazilian regional profile for CYP2D6 polymorphisms and their phenotypes. These findings add to the knowledge of the distribution of different polymorphic CYP2D6 alleles and the potential role of CYP2D6 genotyping in clinical practice prior to choosing therapeutic protocols. Associação Brasileira de Divulgação Científica 2014-09-05 /pmc/articles/PMC4230293/ /pubmed/25296365 http://dx.doi.org/10.1590/1414-431X20143761 Text en http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Clinical Investigation Martins, D.M.F. Vidal, F.C.B. Souza, R.D.M. Brusaca, S.A. Brito, L.M.O. Determination of CYP2D6 *3, *4, and *10 frequency in women with breast cancer in São Luís, Brazil, and its association with prognostic factors and disease-free survival |
title | Determination of CYP2D6 *3, *4, and *10
frequency in women with breast cancer in São Luís, Brazil, and its association with
prognostic factors and disease-free survival |
title_full | Determination of CYP2D6 *3, *4, and *10
frequency in women with breast cancer in São Luís, Brazil, and its association with
prognostic factors and disease-free survival |
title_fullStr | Determination of CYP2D6 *3, *4, and *10
frequency in women with breast cancer in São Luís, Brazil, and its association with
prognostic factors and disease-free survival |
title_full_unstemmed | Determination of CYP2D6 *3, *4, and *10
frequency in women with breast cancer in São Luís, Brazil, and its association with
prognostic factors and disease-free survival |
title_short | Determination of CYP2D6 *3, *4, and *10
frequency in women with breast cancer in São Luís, Brazil, and its association with
prognostic factors and disease-free survival |
title_sort | determination of cyp2d6 *3, *4, and *10
frequency in women with breast cancer in são luís, brazil, and its association with
prognostic factors and disease-free survival |
topic | Clinical Investigation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4230293/ https://www.ncbi.nlm.nih.gov/pubmed/25296365 http://dx.doi.org/10.1590/1414-431X20143761 |
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