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CYP17 gene polymorphism in relation to breast cancer risk: a case-control study

INTRODUCTION: The c.1-34T>C 5' promoter region polymorphism in cytochrome P450c17 (CYP17), a key enzyme in the biosynthesis of estrogen, has been associated with breast cancer risk, but most previous studies have been relatively small. METHODS: We genotyped 1,544 incident cases of primary br...

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Autores principales: Einarsdóttir, Kristjana, Rylander-Rudqvist, Tove, Humphreys, Keith, Ahlberg, Susanne, Jonasdottir, Gudrun, Weiderpass, Elisabete, Chia, Kee Seng, Ingelman-Sundberg, Magnus, Persson, Ingemar, Liu, Jianjun, Hall, Per, Wedrén, Sara
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2005
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1410739/
https://www.ncbi.nlm.nih.gov/pubmed/16280037
http://dx.doi.org/10.1186/bcr1319
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author Einarsdóttir, Kristjana
Rylander-Rudqvist, Tove
Humphreys, Keith
Ahlberg, Susanne
Jonasdottir, Gudrun
Weiderpass, Elisabete
Chia, Kee Seng
Ingelman-Sundberg, Magnus
Persson, Ingemar
Liu, Jianjun
Hall, Per
Wedrén, Sara
author_facet Einarsdóttir, Kristjana
Rylander-Rudqvist, Tove
Humphreys, Keith
Ahlberg, Susanne
Jonasdottir, Gudrun
Weiderpass, Elisabete
Chia, Kee Seng
Ingelman-Sundberg, Magnus
Persson, Ingemar
Liu, Jianjun
Hall, Per
Wedrén, Sara
author_sort Einarsdóttir, Kristjana
collection PubMed
description INTRODUCTION: The c.1-34T>C 5' promoter region polymorphism in cytochrome P450c17 (CYP17), a key enzyme in the biosynthesis of estrogen, has been associated with breast cancer risk, but most previous studies have been relatively small. METHODS: We genotyped 1,544 incident cases of primary breast cancer and 1,502 population controls, all postmenopausal Swedish women, for the CYP17 c.1-34T>C polymorphism and calculated odds ratios (ORs) and 95% confidence intervals (CIs) from logistic regression models. RESULTS: No overall association was found between CYP17 c.1-34T>C and breast cancer risk, OR 1.0 (95% CI 0.8–1.3) for the A2/A2 (CC) carriers compared to the A1/A1 (TT) carriers, regardless of histopathology. We detected an interaction between CYP17 c.1-34T>C and age at menarche (P = 0.026) but regarded that as a chance finding as no dose-response pattern was evident. Other breast cancer risk factors, including menopausal hormone use and diabetes mellitus, did not modify the overall results. CONCLUSION: It is unlikely that CYP17 c.1-34T>C has a role in breast cancer etiology, overall or in combination with established non-genetic breast cancer risk factors.
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spelling pubmed-14107392006-03-24 CYP17 gene polymorphism in relation to breast cancer risk: a case-control study Einarsdóttir, Kristjana Rylander-Rudqvist, Tove Humphreys, Keith Ahlberg, Susanne Jonasdottir, Gudrun Weiderpass, Elisabete Chia, Kee Seng Ingelman-Sundberg, Magnus Persson, Ingemar Liu, Jianjun Hall, Per Wedrén, Sara Breast Cancer Res Research Article INTRODUCTION: The c.1-34T>C 5' promoter region polymorphism in cytochrome P450c17 (CYP17), a key enzyme in the biosynthesis of estrogen, has been associated with breast cancer risk, but most previous studies have been relatively small. METHODS: We genotyped 1,544 incident cases of primary breast cancer and 1,502 population controls, all postmenopausal Swedish women, for the CYP17 c.1-34T>C polymorphism and calculated odds ratios (ORs) and 95% confidence intervals (CIs) from logistic regression models. RESULTS: No overall association was found between CYP17 c.1-34T>C and breast cancer risk, OR 1.0 (95% CI 0.8–1.3) for the A2/A2 (CC) carriers compared to the A1/A1 (TT) carriers, regardless of histopathology. We detected an interaction between CYP17 c.1-34T>C and age at menarche (P = 0.026) but regarded that as a chance finding as no dose-response pattern was evident. Other breast cancer risk factors, including menopausal hormone use and diabetes mellitus, did not modify the overall results. CONCLUSION: It is unlikely that CYP17 c.1-34T>C has a role in breast cancer etiology, overall or in combination with established non-genetic breast cancer risk factors. BioMed Central 2005 2005-09-14 /pmc/articles/PMC1410739/ /pubmed/16280037 http://dx.doi.org/10.1186/bcr1319 Text en Copyright © 2005 Einarsdóttir et al.; licensee BioMed Central Ltd.
spellingShingle Research Article
Einarsdóttir, Kristjana
Rylander-Rudqvist, Tove
Humphreys, Keith
Ahlberg, Susanne
Jonasdottir, Gudrun
Weiderpass, Elisabete
Chia, Kee Seng
Ingelman-Sundberg, Magnus
Persson, Ingemar
Liu, Jianjun
Hall, Per
Wedrén, Sara
CYP17 gene polymorphism in relation to breast cancer risk: a case-control study
title CYP17 gene polymorphism in relation to breast cancer risk: a case-control study
title_full CYP17 gene polymorphism in relation to breast cancer risk: a case-control study
title_fullStr CYP17 gene polymorphism in relation to breast cancer risk: a case-control study
title_full_unstemmed CYP17 gene polymorphism in relation to breast cancer risk: a case-control study
title_short CYP17 gene polymorphism in relation to breast cancer risk: a case-control study
title_sort cyp17 gene polymorphism in relation to breast cancer risk: a case-control study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1410739/
https://www.ncbi.nlm.nih.gov/pubmed/16280037
http://dx.doi.org/10.1186/bcr1319
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