Reference : Recombinant human estrogen, androgen and progesterone receptors for detection of potenti...
Scientific journals : Article
Life sciences : Biochemistry, biophysics & molecular biology
Physical, chemical, mathematical & earth Sciences : Chemistry
http://hdl.handle.net/2268/8706
Recombinant human estrogen, androgen and progesterone receptors for detection of potential endocrine disruptors
English
Scippo, Marie-Louise mailto [Université de Liège - ULg > Département de sciences des denrées alimentaires > Analyse des denrées alimentaires >]
Argiris, Catherine [> > > >]
Van de Weerdt, Cécile mailto [Université de Liège - ULg > Département des sciences de la vie > Biologie et génétique moléculaire >]
Muller, Marc mailto [Université de Liège - ULg > Département des sciences de la vie > Biologie et génétique moléculaire >]
Willemsen, Philippe [> > > >]
Martial, Joseph mailto [Université de Liège - ULg > Département des sciences de la vie > Biologie et génétique moléculaire >]
Maghuin-Rogister, Guy mailto [Université de Liège - ULg > Département de sciences des denrées alimentaires > Département de sciences des denrées alimentaires >]
2004
Analytical and Bioanalytical Chemistry
Springer-Verlag Heidelberg
378
3
664-669
International
1618-2642
Heidelberg
[en] endocrine disruptors ; steroid receptors ; binding assay ; pesticides ; radioreceptor assay
[en] This work reports the binding capacity of various chemicals (so-called endocrine disruptors) to recombinant human steroid receptors (hERalpha, hPR and hAR). The tested chemicals are organochlorine insecticides (DDT and its metabolites, methoxychlor, aldrin, dieldrin, chlordecone, lindane, trichlorobenzene), estrogenic insecticides (endosulfan, toxaphene, nonachlor), herbicides (alachlor and atrazine), fungicides (benomyl and vinclozolin), industrial chemicals (nonylphenol, bisphenol A, diphenylphtalate), antioxidants (butylated hydroxyanisol) and some phytoestrogens. Except for phytoestrogens, most of the tested chemicals (DDT and its metabolites, aldrin, alpha- and beta-endosulfan, toxaphen, trans-nonachlor) show higher affinities for hPR than for hERalpha, indicating that the interaction with the progesterone receptor could contribute to the endocrine-disrupting effects imputed to these chemicals. We propose to use binding assays using recombinant human steroid receptors as screening tools for the detection of endocrine disruptors in various samples.
http://hdl.handle.net/2268/8706

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