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Structure-dependent Ah receptor agonist activities of chlorinated biphenylenes.

Authors :
Khan S
Konstantinov A
Chittim B
McAlees A
Yeo B
Safe S
Source :
Toxicology in vitro : an international journal published in association with BIBRA [Toxicol In Vitro] 2006 Oct; Vol. 20 (7), pp. 1234-7. Date of Electronic Publication: 2006 May 03.
Publication Year :
2006

Abstract

Polychlorinated biphenylenes (PCBP) have been identified as combustion by-products that bind the aryl hydrocarbon receptor (AhR) and exhibit 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD)-like activity. This study investigates the Ah-responsiveness of 2,3,6,7-tetrachlorobiphenylene (2,3,6,7-CBP), 2,3,6-CBP, 2,3-CBP and 2-CBP in breast cancer cells. MCF-7 or ZR-75 cells were treated with different concentrations (1-100 nM) of the compounds alone to determine their activity as inducers of CYP1A1 protein expression or luciferase activity in cells transfected with a construct (pDRE(3)) containing three tandem dioxin responsive elements (DREs) linked to a luciferase reporter gene. In both assays, the order of potency was 2,3,6,7-CBP>2,3,6-CBP>2,3-CBP approximately 2-CBP, and 2,3,6,7-CBP and TCDD were equipotent. Similar results were also observed in an antiestrogenic assay in MCF-7 cells, confirming the high AhR agonist activity of 2,3,6,7-CBP in breast cancer cells.

Details

Language :
English
ISSN :
0887-2333
Volume :
20
Issue :
7
Database :
MEDLINE
Journal :
Toxicology in vitro : an international journal published in association with BIBRA
Publication Type :
Academic Journal
Accession number :
16759834
Full Text :
https://doi.org/10.1016/j.tiv.2006.04.003