In vitro estrogenic and antiestrogenic potential of chlorostyrenes

被引:3
|
作者
Oh, Seung Min [1 ]
Kim, Ha Ryong [1 ]
Chung, Kyu Hyuck [1 ]
机构
[1] Sungkyunkwan Univ, Coll Pharm, Suwon 440746, Gyeonggi Do, South Korea
关键词
Chlorostyrene; Anti-/estrogenic activity; E-SCREEN assay; Aromatase activity; E-2; metabolism; BREAST-CANCER-CELLS; BISPHENOL-A; POLYCHLORINATED STYRENES; GENE-EXPRESSION; RISK-ASSESSMENT; MCF-7; CELLS; ER-ALPHA; FISH; ASSAY; CHEMICALS;
D O I
10.1016/j.tiv.2009.07.032
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Chlorostyrenes (CSs) are primarily derived from industrial by-products and are persistent and accumulative in the environment. In this study, the estrogenic and antiestrogenic activities of CSs (0-CS, m-CS, P-CS, DiCS, octa-CS) were evaluated using in vitro bioassays. o-CS and octa-CS have both estrogenic and antiestrogenic activity in the E-SCREEN assay and the ERE-reporter gene assay, indicating effects on a classical ER-mediated pathway. m-CS showed estrogenic activity in E-SCREEN but not in ERE-reporter gene assays, indicating that it may work through a non-classical ER-mediated pathway. Finally, DiCS only showed antiestrogenic activity via an ER-independent pathway, which can be induced by depletion of endogenous E-2 level by the inhibition of aromatase activity and the stimulation of E2 metabolism. Although CSs have structural similarities to dioxins/furans, they did not have AhR agonist effects. This study is the first to show the estrogenic and antiestrogenic activity of several CSs using in vitro bioassay systems, including whether the compounds work via ER-mediated or/and non-ER-mediated pathways. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1242 / 1248
页数:7
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