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首页> 外文期刊>International Journal of Cancer =: Journal International du Cancer >Alcohol consumption and risk of breast cancer by molecular subtype: Prospective analysis of the nurses' health study after 26 years of follow-up
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Alcohol consumption and risk of breast cancer by molecular subtype: Prospective analysis of the nurses' health study after 26 years of follow-up

机译:酒精摄入量和按分子亚型分类的乳腺癌风险:26年随访后护士健康研究的前瞻性分析

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Alcohol consumption is a consistent risk factor for breast cancer, although it is unclear whether the association varies by breast cancer molecular subtype. We investigated associations between cumulative average alcohol intake and risk of breast cancer by molecular subtype among 105,972 women in the prospective Nurses' Health Study cohort, followed from 1980 to 2006. Breast cancer molecular subtypes were defined according to estrogen receptor (ER), progesterone receptor, human epidermal growth factor 2 (HER2), cytokeratin 5/6, and epidermal growth factor status from immunostained tumor microarrays in combination with histologic grade. Multivariable Cox proportional hazards models were used to estimate hazard ratios (HR) and 95% confidence intervals (CI). Competing risk analyses were used to assess heterogeneity by subtype. We observed suggestive heterogeneity in associations between alcohol and breast cancer by subtype (p(het)=0.06). Alcohol consumers had an increased risk of luminal A breast cancers [n=1,628 cases, per 10 g/day increment HR (95% CI) 51.10(1.05-1.15)], and an increased risk that was suggestively stronger for HER2-type breast cancer [n=160 cases, HR (95% CI) 51.16(1.02-1.33)]. We did not observe statistically significant associations between alcohol and risk of luminal B [n=631 cases, HR (95% CI) 51.08(0.99-1.16)], basal-like [n=254 cases, HR (95% CI) 50.90(0.77-1.04)], or unclassified [n=87 cases, HR (95% CI) 50.90(0.71-1.14)] breast cancer. Alcohol consumption was associated with increased risk of luminal A and HER2-type breast cancer, but not significantly associated with other subtypes. Given that ERs are expressed in luminal A but not in HER2-type tumors, our findings suggest that other mechanisms may play a role in the association between alcohol and breast cancer.
机译:饮酒是乳腺癌的一贯危险因素,尽管尚不清楚该关联是否因乳腺癌分子亚型而异。我们调查了前瞻性“护士健康研究”队列中105972名妇女的平均平均酒精摄入量与乳腺癌风险之间的相关性(按分子亚型),方法是从1980年至2006年。乳腺癌的分子亚型是根据雌激素受体(ER)和孕激素受体定义的免疫染色的肿瘤微阵列结合组织学分级可确定人表皮生长因子2(HER2),细胞角蛋白5/6和表皮生长因子的状态。使用多变量Cox比例风险模型估计风险比(HR)和95%置信区间(CI)。竞争风险分析用于评估亚型的异质性。我们观察到酒精与乳腺癌之间亚型之间的关联存在暗示异质性(p(het)= 0.06)。饮酒的人患上管腔A型乳腺癌的风险增加[n = 1,628例,每10 g /天的HR(95%CI)51.10(1.05-1.15)],并且提示HER2型乳腺癌的风险增加癌症[n = 160例,HR(95%CI)51.16(1.02-1.33)]。我们没有观察到酒精与管腔B风险之间的统计学显着相关性[n = 631例,HR(95%CI)51.08(0.99-1.16)],基底样[n = 254例,HR(95%CI)50.90 (0.77-1.04)]或未分类[n = 87例,HR(95%CI)50.90(0.71-1.14)]乳腺癌。饮酒与管腔A和HER2型乳腺癌的风险增加相关,但与其他亚型无显着相关性。鉴于内质网在腔A中表达,但在HER2型肿瘤中不表达,我们的发现表明,其他机制可能在酒精与乳腺癌之间的关联中起作用。

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