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Manganese superoxide dismutase Ala-9Val polymorphism and risk of breast cancer in a population-based case–control study of African Americans and whites

INTRODUCTION: A polymorphism in the manganese superoxide dismutase (MnSOD) gene, Ala-9Val, has been examined in association with breast cancer risk in several epidemiologic studies. Results suggest that the Ala allele increases the risk of breast cancer and modifies the effects of environmental expo...

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Autores principales: Millikan, Robert C, Player, Jon, de Cotret, Allan René, Moorman, Patricia, Pittman, Gary, Vannappagari, Vani, Tse, Chiu-Kit J, Keku, Temitope
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2004
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC468618/
https://www.ncbi.nlm.nih.gov/pubmed/15217492
http://dx.doi.org/10.1186/bcr786
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author Millikan, Robert C
Player, Jon
de Cotret, Allan René
Moorman, Patricia
Pittman, Gary
Vannappagari, Vani
Tse, Chiu-Kit J
Keku, Temitope
author_facet Millikan, Robert C
Player, Jon
de Cotret, Allan René
Moorman, Patricia
Pittman, Gary
Vannappagari, Vani
Tse, Chiu-Kit J
Keku, Temitope
author_sort Millikan, Robert C
collection PubMed
description INTRODUCTION: A polymorphism in the manganese superoxide dismutase (MnSOD) gene, Ala-9Val, has been examined in association with breast cancer risk in several epidemiologic studies. Results suggest that the Ala allele increases the risk of breast cancer and modifies the effects of environmental exposures that produce oxidative damage to DNA. METHODS: We examined the role of the MnSOD Ala-9Val polymorphism in a population-based case–control study of invasive and in situ breast cancer in North Carolina. Genotypes were evaluated for 2025 cases (760 African Americans and 1265 whites) and for 1812 controls (677 African Americans and 1135 whites). RESULTS: The odds ratio for MnSOD Ala/Ala versus any MnSOD Val genotypes was not elevated in African Americans (odds ratio = 0.9, 95% confidence interval = 0.7–1.2) or in whites (odds ratio = 1.0, 95% confidence interval = 0.8–1.2). Greater than additive joint effects were observed for the Ala/Ala genotype and smoking, radiation to the chest, and occupational exposure to ionizing radiation. Antagonism was observed between the Ala/Ala genotype and the use of nonsteroidal anti-inflammatory drugs. CONCLUSIONS: The MnSOD genotype may contribute to an increased risk of breast cancer in the presence of specific environmental exposures. These results provide further evidence for the importance of reactive oxygen species and of oxidative DNA damage in the etiology of breast cancer.
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spelling pubmed-4686182004-07-16 Manganese superoxide dismutase Ala-9Val polymorphism and risk of breast cancer in a population-based case–control study of African Americans and whites Millikan, Robert C Player, Jon de Cotret, Allan René Moorman, Patricia Pittman, Gary Vannappagari, Vani Tse, Chiu-Kit J Keku, Temitope Breast Cancer Res Research Article INTRODUCTION: A polymorphism in the manganese superoxide dismutase (MnSOD) gene, Ala-9Val, has been examined in association with breast cancer risk in several epidemiologic studies. Results suggest that the Ala allele increases the risk of breast cancer and modifies the effects of environmental exposures that produce oxidative damage to DNA. METHODS: We examined the role of the MnSOD Ala-9Val polymorphism in a population-based case–control study of invasive and in situ breast cancer in North Carolina. Genotypes were evaluated for 2025 cases (760 African Americans and 1265 whites) and for 1812 controls (677 African Americans and 1135 whites). RESULTS: The odds ratio for MnSOD Ala/Ala versus any MnSOD Val genotypes was not elevated in African Americans (odds ratio = 0.9, 95% confidence interval = 0.7–1.2) or in whites (odds ratio = 1.0, 95% confidence interval = 0.8–1.2). Greater than additive joint effects were observed for the Ala/Ala genotype and smoking, radiation to the chest, and occupational exposure to ionizing radiation. Antagonism was observed between the Ala/Ala genotype and the use of nonsteroidal anti-inflammatory drugs. CONCLUSIONS: The MnSOD genotype may contribute to an increased risk of breast cancer in the presence of specific environmental exposures. These results provide further evidence for the importance of reactive oxygen species and of oxidative DNA damage in the etiology of breast cancer. BioMed Central 2004 2004-04-07 /pmc/articles/PMC468618/ /pubmed/15217492 http://dx.doi.org/10.1186/bcr786 Text en Copyright © 2004 Millikan et al., licensee BioMed Central Ltd. This is an Open Access article: verbatim copying and redistribution of this article are permitted in all media for any purpose, provided this notice is preserved along with the article's original URL.
spellingShingle Research Article
Millikan, Robert C
Player, Jon
de Cotret, Allan René
Moorman, Patricia
Pittman, Gary
Vannappagari, Vani
Tse, Chiu-Kit J
Keku, Temitope
Manganese superoxide dismutase Ala-9Val polymorphism and risk of breast cancer in a population-based case–control study of African Americans and whites
title Manganese superoxide dismutase Ala-9Val polymorphism and risk of breast cancer in a population-based case–control study of African Americans and whites
title_full Manganese superoxide dismutase Ala-9Val polymorphism and risk of breast cancer in a population-based case–control study of African Americans and whites
title_fullStr Manganese superoxide dismutase Ala-9Val polymorphism and risk of breast cancer in a population-based case–control study of African Americans and whites
title_full_unstemmed Manganese superoxide dismutase Ala-9Val polymorphism and risk of breast cancer in a population-based case–control study of African Americans and whites
title_short Manganese superoxide dismutase Ala-9Val polymorphism and risk of breast cancer in a population-based case–control study of African Americans and whites
title_sort manganese superoxide dismutase ala-9val polymorphism and risk of breast cancer in a population-based case–control study of african americans and whites
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC468618/
https://www.ncbi.nlm.nih.gov/pubmed/15217492
http://dx.doi.org/10.1186/bcr786
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