TY - JOUR
T1 - Nongenomic signaling pathways of estrogen toxicity
AU - Watson, Cheryl S.
AU - Jeng, Yow Jiun
AU - Kochukov, Mikhail Y.
PY - 2010/5
Y1 - 2010/5
N2 - 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.
AB - 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.
KW - Membrane estrogen receptors
KW - Signaling
KW - Xenoestrogen
UR - http://www.scopus.com/inward/record.url?scp=79551682463&partnerID=8YFLogxK
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U2 - 10.1093/toxsci/kfp288
DO - 10.1093/toxsci/kfp288
M3 - Review article
C2 - 19955490
AN - SCOPUS:79551682463
SN - 1096-6080
VL - 115
SP - 1
EP - 11
JO - Toxicological Sciences
JF - Toxicological Sciences
IS - 1
ER -