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

Lydia Lichtiger, Janelle A. Rivera, Debashish Sahay, Rachel L. Miller
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引用次数: 1

Abstract

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.
多环芳烃与乳腺癌风险:肥胖也有关系吗?
乳腺癌症的风险仍然没有得到完全解释,近年来以及城市和工业化地区癌症的发病率较高表明是环境原因。多环芳烃(PAH)在环境中普遍存在,流行病学和啮齿类动物研究表明,接触PAH与乳腺癌症发病率以及乳腺肿瘤发生之间存在关联。此外,在有限的实验研究中,体外和啮齿类动物研究表明,PAH暴露后雌激素受体α(Erα)信号通路发生了变化。然而,我们对这些机制的理解是不完整的。Sahay等人通过研究PAH暴露对暴露于城市空气中测量比例的雾化PAH的小鼠队列中Erα通路基因的表观遗传学和转录调控的影响,解决了这一差距。除了怀孕小鼠及其后代和孙子女的Erα信号通路发生变化外,研究人员还观察到,与对照组相比,暴露于PAH的小鼠体重更高。鉴于先前已观察到乳腺组织肥胖、全身性肥胖和乳腺癌症风险之间的相关性,PAH暴露组中较高体重的发现增加了体重可能影响PAH暴露与乳腺癌症风险之间的关联的可能性。除了新的分析外,我们还讨论了体重可能改变后代和孙代小鼠PAH暴露、乳腺细胞增殖和乳腺导管增生之间关系的可能性,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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