多环芳烃与乳腺癌风险:肥胖也有关系吗?

Journal of cancer immunology Pub Date : 2021-01-01
Lydia Lichtiger, Janelle Rivera, Debashish Sahay, Rachel L Miller
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引用次数: 0

摘要

乳腺癌风险仍未完全解释清楚,近年来城市和工业化地区乳腺癌发病率较高表明是环境原因。多环芳烃(PAH)在环境中无处不在,流行病学和啮齿动物研究表明,多环芳烃暴露与乳腺癌发病率和乳腺肿瘤发生之间存在关联。此外,在有限的实验研究中,体外和啮齿动物研究表明多环芳烃暴露后雌激素受体α (Erα)信号通路发生了改变。然而,我们对这些机制的理解并不完整。Sahay等人通过研究多环芳烃暴露对Erα途径中基因表观遗传和转录调控的影响,解决了这一差距,研究对象是在城市空气中测量比例暴露于雾化多环芳烃的小鼠队列。除了怀孕小鼠及其后代和后代的Erα信号通路发生改变外,研究人员还观察到,与对照组相比,暴露于多环芳烃的小鼠体重增加。鉴于乳腺组织脂肪、全身性脂肪和乳腺癌风险之间的关联此前已被观察到,多环芳烃暴露组中体重较高的发现提出了体重可能影响多环芳烃暴露与乳腺癌风险之间关联的可能性。随着新的分析,我们讨论了体重可能改变后代和后代小鼠多环芳烃暴露、乳腺细胞增殖和乳腺导管增生之间的关系的可能性,以及未来可能需要的研究来描述这些关系。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Polycyclic Aromatic Hydrocarbons and Mammary Cancer Risk: Does Obesity Matter too?

Breast cancer risk remains incompletely explained, and higher incidence rates of breast cancer over recent times and in urban and industrialized areas suggest environmental causes. Polycyclic aromatic hydrocarbons (PAH) are ubiquitous in the environment and epidemiological and rodent studies have shown associations between exposure to PAH and breast cancer incidence as well as mammary tumorigenesis. In addition, in vitro and rodent studies have implicated alterations in estrogen receptor alpha (Erα) signaling pathways following PAH exposure in limited experimental studies. However, our understanding of these mechanisms is incomplete. Sahay et al. addressed this gap by examining the effect of PAH exposure on epigenetic and transcriptional regulation of genes in the Erα pathway in a mouse cohort exposed to aerosolized PAH at proportions measured in urban air. In addition to alterations in the Erα signaling pathway in the pregnant mice and in their offspring and grandoffspring, the investigators observed higher body weights in mice exposed to PAH compared to the control. Given that associations between mammary tissue adiposity, systemic adiposity, and breast cancer risk have been observed previously, the finding of higher body weight in the PAH exposure group raises the possibility that body weight might influence the association between PAH exposure and breast cancer risk. Along with new analyses, we discuss the possibility that body weight may modify the association between PAH exposure, mammary cellular proliferation, and mammary gland ductal hyperplasia in offspring and grandoffspring mice and future research that may be needed to delineate these associations.

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