护士健康研究中绝经后妇女雌激素活性与浸润性乳腺癌风险的关系

Etienne X Holder, Serena C Houghton, Sylvia S Sanchez, A Heather Eliassen, Jing Qian, Elizabeth R Bertone-Johnson, Zhenhua Liu, Shelley S Tworoger, Martyn T Smith, Susan E Hankinson
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引用次数: 2

摘要

背景:雌激素通过雌激素受体(ER)介导的通路激活增加乳腺癌风险。目前尚不清楚是否对导致内质网激活的血浆化合物进行更广泛的评估会比测量个体雌激素与风险的关系更密切。方法:在护士健康研究中对绝经后妇女进行前瞻性巢式病例对照研究,其中包括371例乳腺癌诊断前采集的血液样本和731例匹配的对照。利用经血浆处理的T47D-Kbluc (ATCC)人乳腺癌细胞,通过荧光素酶报告基因检测评估总雌激素通路活性(EA)。我们还评估了EA对风险的贡献,独立于循环雌酮、雌二醇和硫酸雌酮浓度。采用调整乳腺癌危险因素的条件logistic回归计算多变量ORs和95%置信区间(CI)。结果:EA最高四分位数的女性与最低四分位数的女性相比,浸润性乳腺癌的风险增加了86% (ORQ4vsQ1, 1.86;95% ci = 1.16-2.97)。仅考虑雌二醇后,观察到较弱的相关性(ORQ4vsQ1, 1.27;95% ci = 0.75-2.17)。在考虑了所有三种雌激素后,没有发现相关性(ORQ4vsQ1, 1.01;95% ci = 0.56-1.84)。结论:EA与乳腺癌风险呈正相关。然而,在考虑了其他雌激素的水平后,这种联系大大减弱了。影响:我们的研究首次提供了基于乳腺癌细胞系的EA测定和绝经后乳腺癌风险的详细评估。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Estrogenic Activity and Risk of Invasive Breast Cancer Among Postmenopausal Women in the Nurses' Health Study.

Background: Estrogens increase breast cancer risk through estrogen receptor (ER)-mediated pathway activation. It is unclear whether a broader assessment of plasma compounds that lead to ER activation would be more strongly related to risk than measurement of individual estrogens.

Methods: A prospective nested case-control study was conducted among postmenopausal women in the Nurses' Health Study, that included 371 cases with blood samples collected prior to breast cancer diagnosis and 731 matched controls. Total estrogen pathway activity (EA) was assessed via a luciferase reporter assay using plasma-treated T47D-Kbluc (ATCC) human breast cancer cells. We also assessed the contribution of EA to risk, independent of circulating estrone, estradiol, and estrone sulfate concentrations. Multivariable ORs and 95% confidence intervals (CI) were calculated using conditional logistic regression adjusting for breast cancer risk factors.

Results: Women in the highest, versus lowest EA quartile had an 86% increased risk of invasive breast cancer (ORQ4vsQ1, 1.86; 95% CI = 1.16-2.97). After accounting for estradiol only, a weaker association was observed (ORQ4vsQ1, 1.27; 95% CI = 0.75-2.17). No association was observed after accounting for all three estrogens (ORQ4vsQ1, 1.01; 95% CI = 0.56-1.84).

Conclusions: A positive association between EA and breast cancer risk was observed. However, the association was substantially attenuated after accounting for levels of other estrogens.

Impact: Our study provides a first detailed assessment of a breast cancer cell line-based EA assay and postmenopausal breast cancer risk.

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