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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

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TLDR
The MnSOD genotype may contribute to an increased risk of breast cancer in the presence of specific environmental exposures and provide further evidence for the importance of reactive oxygen species and of oxidative DNA damage in the etiology of Breast cancer.
Abstract
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. 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). 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. 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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Trends in oxidative aging theories

TL;DR: It is argued that a tentative case for oxidative stress as a life-span determinant can be made in Drosophila melanogaster, and where the free radical theory is headed is discussed, specifically, telomere/cell senescence, genomic instability, and the mitochondrial hypothesis of aging.
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Mitochondrial DNA G10398A polymorphism and invasive breast cancer in African-American women.

TL;DR: Novel epidemiologic evidence is provided that the mtDNA 10398A allele influences breast cancer susceptibility in African-American women and underappreciated factors in breast carcinogenesis are identified.
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Breast Cancer in African-American Women

TL;DR: African- American women face a lower risk of being diagnosed with breast cancer as compared to Caucasian-American women, yet they paradoxically face an increased breast cancer mortality hazard.
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Mitochondrial DNA G10398A polymorphism and invasive breast cancer in African-American women. Authors' reply

TL;DR: The mtDNA G10398A polymorphism alters the structure of Complex I in the mitochondrial electron transport chain, an important site of free radical production and is associated with several neurodegenerative disorders.
References
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Oxidative DNA damage: mechanisms, mutation, and disease

TL;DR: This review critically addresses the extent to which the in vitro significance of oxidative DNA damage has relevance for the pathogenesis of disease, drawing attention to the multiplicity of proteins with repair activities along with a number of poorly considered effects of damage.
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Replication validity of genetic association studies.

TL;DR: It is concluded that a systematic meta-analytic approach may assist in estimating population-wide effects of genetic risk factors in human disease.
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Problems of reporting genetic associations with complex outcomes.

TL;DR: It is suggested that the most important factors underlying inability to replicate these associations are publication bias, failure to attribute results to chance, and inadequate sample sizes, problems that are all rectifiable.
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Biomarkers of free radical damage: Applications in experimental animals and in humans

TL;DR: This review gives an overview of the applications in experimental and human situations of four main groups of products resulting from free radical damage, these include: lipid peroxidation products, isoprostanes, DNA-hydroxylation products and protein hydroxylated products.
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Genetic associations in large versus small studies: an empirical assessment.

TL;DR: How often large studies arrive at different conclusions than smaller studies is assessed, and whether this situation arises more frequently when findings of first published studies disagree with those of subsequent research is assessed.
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