THE ANTIESTROGENIC ACTIVITY OF SELECTED POLYNUCLEAR AROMATIC-HYDROCARBONS IN YEAST EXPRESSING HUMAN ESTROGEN-RECEPTOR

Citation
Dq. Tran et al., THE ANTIESTROGENIC ACTIVITY OF SELECTED POLYNUCLEAR AROMATIC-HYDROCARBONS IN YEAST EXPRESSING HUMAN ESTROGEN-RECEPTOR, Biochemical and biophysical research communications, 229(1), 1996, pp. 102-108
Citations number
14
Categorie Soggetti
Biology,Biophysics
ISSN journal
0006291X
Volume
229
Issue
1
Year of publication
1996
Pages
102 - 108
Database
ISI
SICI code
0006-291X(1996)229:1<102:TAAOSP>2.0.ZU;2-T
Abstract
Polynuclear aromatic hydrocarbons (PAH) represent a large class of che micals present in the environment. We have used yeast strain ER(wt) ex pressing human estrogen receptor (hER) and an estrogen-sensitive repor ter to characterize the estrogenic or anti-estrogenic activities of 21 PAHs. The PAHs did not exhibit estrogenic activity in yeast strain ER (wt). Four of the PAHs, dibenz[a,h]anthracene, 6-hydroxy-chrysene, 2,3 -benzofluorene, and benzo(a)pyrene, inhibited estradiol-dependent repo rter activity in strain ER(wt). A mutant hER lacking the amino terminu s expressed in yeast was inhibited by the four PAHs to a lesser extent than the full-length hER. 6-hydroxy-chrysene, 2,3-benzofluorene, and benzo(a)pyrene, but not dibenz[a,h]anthracene, weakly displaced [H-3]e stradiol from the hER in a competition binding assay. A strong correla tion between the inhibition of [H-3]estradiol-binding from the hER and the reduction of hER-mediated transactivation in yeast was not observ ed. These observations suggest that the PAHs dibenz[a,h,]-anthracene, 6-hydroxy-chrysene, 2,3-benzofluorene, and benzo(a)pyrene may antagoni ze estradiol activity in yeast by binding to an anti-estrogen binding site on the hER or by mechanisms independent of the hER. (C) 1996 Acad emic Press, Inc.