Study Centre for Carcinogenesis and Primary Prevention of Cancer, Department of Radiotherapy and Experimental Cancerology, Ghent University Hospital, De Pintelaan 185 3K3, 9000 Ghent, Belgium.
J Environ Public Health. 2012;2012:713696. doi: 10.1155/2012/713696. Epub 2012 Sep 6.
The incidence and/or prevalence of health problems associated with endocrine-disruption have increased. Many chemicals have endocrine-disrupting properties, including bisphenol A, some organochlorines, polybrominated flame retardants, perfluorinated substances, alkylphenols, phthalates, pesticides, polycyclic aromatic hydrocarbons, alkylphenols, solvents, and some household products including some cleaning products, air fresheners, hair dyes, cosmetics, and sunscreens. Even some metals were shown to have endocrine-disrupting properties. Many observations suggesting that endocrine disruptors do contribute to cancer, diabetes, obesity, the metabolic syndrome, and infertility are listed in this paper. An overview is presented of mechanisms contributing to endocrine disruption. Endocrine disruptors can act through classical nuclear receptors, but also through estrogen-related receptors, membrane-bound estrogen-receptors, and interaction with targets in the cytosol resulting in activation of the Src/Ras/Erk pathway or modulation of nitric oxide. In addition, changes in metabolism of endogenous hormones, cross-talk between genomic and nongenomic pathways, cross talk with estrogen receptors after binding on other receptors, interference with feedback regulation and neuroendocrine cells, changes in DNA methylation or histone modifications, and genomic instability by interference with the spindle figure can play a role. Also it was found that effects of receptor activation can differ in function of the ligand.
与内分泌干扰相关的健康问题的发病率和/或流行率有所增加。许多化学物质具有内分泌干扰特性,包括双酚 A、某些有机氯化合物、多溴阻燃剂、全氟化合物、烷基酚、邻苯二甲酸酯、农药、多环芳烃、烷基酚、溶剂以及一些家用产品,包括一些清洁产品、空气清新剂、染发剂、化妆品和防晒霜。甚至一些金属也被证明具有内分泌干扰特性。本文列出了许多表明内分泌干扰物确实会导致癌症、糖尿病、肥胖、代谢综合征和不孕的观察结果。本文概述了导致内分泌干扰的机制。内分泌干扰物可以通过经典的核受体发挥作用,但也可以通过雌激素相关受体、膜结合的雌激素受体以及与细胞质中的靶标相互作用发挥作用,从而激活Src/Ras/Erk 途径或调节一氧化氮。此外,内源性激素代谢的变化、基因组和非基因组途径之间的串扰、与其他受体结合后与雌激素受体的串扰、干扰反馈调节和神经内分泌细胞、DNA 甲基化或组蛋白修饰的变化以及通过干扰纺锤体形态的基因组不稳定性都可能发挥作用。还发现,受体激活的效应在配体的功能上可能不同。