Nongenomic Signaling Pathways of Estrogen Toxicity

被引:62
作者
Watson, Cheryl S. [1 ]
Jeng, Yow-Jiun [1 ]
Kochukov, Mikhail Y. [1 ]
机构
[1] Univ Texas Med Branch, Dept Biochem & Mol Biol, Galveston, TX 77555 USA
关键词
xenoestrogen; membrane estrogen receptors; signaling; BREAST-CANCER CELLS; PITUITARY-TUMOR CELLS; RECEPTOR-ALPHA LEVELS; ACTIVITY IN-VITRO; BISPHENOL-A; ER-ALPHA; ENVIRONMENTAL CHEMICALS; PARKINSONS-DISEASE; PROLACTIN-RELEASE; MAMMARY-CANCER;
D O I
10.1093/toxsci/kfp288
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Xenoestrogens can affect the healthy functioning of a variety of tissues by acting as potent estrogens via nongenomic signaling pathways or by interfering with those actions of multiple physiological estrogens. Collectively, our and other studies have compared a wide range of estrogenic compounds, including some closely structurally related subgroups. The estrogens that have been studied include environmental contaminants of different subclasses, dietary estrogens, and several prominent physiological metabolites. By comparing the nongenomic signaling and functional responses to these compounds, we have begun to address the structural requirements for their actions through membrane estrogen receptors in the pituitary, in comparison to other tissues, and to gain insights into their typical non-monotonic dose-response behavior. Their multiple inputs into cellular signaling begin processes that eventually integrate at the level of mitogen-activated protein kinase activities to coordinately regulate broad cellular destinies, such as proliferation, apoptosis, or differentiation.
引用
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页码:1 / 11
页数:11
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