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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...
Autores principales: | , , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2005
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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. |
format | Text |
id | pubmed-1410739 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2005 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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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