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Environmental Health Perspectives Volume 104, Number 10, October 1996 Open Access
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Identification of Environmental Chemicals with Estrogenic Activity Using a Combination of In Vitro Assays

Diane M. Klotz,1,2 Barbara S. Beckman,1,2,3,4 Steven M. Hill,1,2,4,5 John A. McLachlan,1,2,3,4,6 Marian R. Walters,1,2,4,7 and Steven F. Arnold1,2,4,6

1Tulane-Xavier Center for Bioenvironmental Research; 2Tulane Cancer Center; 3Department of Pharmacology, 4Molecular and Cellular Biology Program, and 5Department of Anatomy, Tulane University Medical Center; 6Department of Environmental Health Sciences, Tulane University School of Public Health and Tropical Medicine; 7Department of Physiology, Tulane University Medical Center, New Orleans, LA 70112 USA

Abstract

Environmental chemicals that function as estrogens have been suggested to be associated with an increase in disease and dysfunctions in animals and humans. To characterize chemicals that may act as estrogens in humans, we have compared three in vitro assays which measure aspects of human estrogen receptor (hER) -mediated estrogenicity. Chemicals were first tested for estrogen-associated transcriptional activity in the yeast estrogen screen (YES) . This was created by expressing hER and two estrogen response elements linked to the lacZ gene in yeast. Second, chemicals that were tested in YES were then assayed for direct interaction with hER in a competition binding assay. Third, chemicals were tested in the estrogen-responsive MCF-7 human breast cancer cell line transiently transfected with a plasmid containing two estrogen response elements linked to the luciferase gene. Together, these assays have identified two metabolites of DDT, o,p´-DDD and p,p´-DDD, that have estrogenic activity. Interestingly, previous studies had reported that the DDD metabolites were nonestrogenic in whole animal models. Alachlor, the most frequently used herbicide in the United States, cis-nonachlor, and trans-nonachlor displayed weak estrogenic activity in the combined assays. The antifungal agent benomyl had no estrogenic activity. We propose that a combination of in vitro assays can be used in conjunction with whole animal models for a more complete characterization of chemicals with estrogenic activity. Key words: , , , , . Environ Health Perspect 104:1084-1089 (1996)


Address correspondence to S. F. Arnold, Tulane-Xavier Center for Bioenvironmental Research, 1430 Tulane Ave. SL3, New Orleans, LA 70112 USA.

We would like to thank Louis Guillette, Bill Toscano, Peter Vonier, and Bridgette Collins for comments on the manuscript. This work was supported by the Louisiana Breast Cancer Task Force, the Tulane Cancer Center, and the Tulane-Xavier Center for Bioenvironmental Research.

Received 19 March 1996 ; accepted 29 May 1996.


The full version of this article is available for free in HTML format.
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