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Glyceollins and dehydroglyceollins isolated from soybean act as SERMs and ER subtype-selective phytoestrogens.
van de Schans, Milou G M; Vincken, Jean-Paul; de Waard, Pieter; Hamers, Astrid R M; Bovee, Toine F H; Gruppen, Harry.
Affiliation
  • van de Schans MG; Laboratory of Food Chemistry, Wageningen University, Wageningen, The Netherlands.
  • Vincken JP; Laboratory of Food Chemistry, Wageningen University, Wageningen, The Netherlands. Electronic address: jean-paul.vincken@wur.nl.
  • de Waard P; Wageningen NMR Centre, Wageningen University, Wageningen, The Netherlands.
  • Hamers AR; Business Unit of Toxicology and Bioassays, RIKILT-Institute of Food Safety, Wageningen, The Netherlands.
  • Bovee TF; Business Unit of Toxicology and Bioassays, RIKILT-Institute of Food Safety, Wageningen, The Netherlands.
  • Gruppen H; Laboratory of Food Chemistry, Wageningen University, Wageningen, The Netherlands.
J Steroid Biochem Mol Biol ; 156: 53-63, 2016 Feb.
Article de En | MEDLINE | ID: mdl-26655113
ABSTRACT
Seven prenylated 6a-hydroxy-pterocapans and five prenylated 6a,11a-pterocarpenes with different kinds of prenylation were purified from an ethanolic extract of fungus-treated soybean sprouts. The activity of these compounds toward both human estrogen receptors (hERα and hERß) was determined in a yeast bioassay and the activity toward hERα was additionally tested in an U2-OS based hERα CALUX bioassay. In the yeast bioassay, compounds with chain prenylation showed in general an agonistic mode of action toward hERα, whereas furan and pyran prenylation led to an antagonistic mode of action. Five of these antagonistic compounds had an agonistic mode of action in the U2-OS based hERα CALUX bioassay, implying that these compounds can act as SERMs. The yeast bioassay also identified 8 ER subtype-selective compounds, with either an antagonistic mode of action or no response toward hERα and an agonistic mode of action toward hERß. The ER subtype-selective compounds were characterized by 6a-hydroxy-pterocarpan or 6a,11a-pterocarpene backbone structure. It is suggested that either the extra D-ring or the increase in length to 12-13.5Å of these compounds is responsible for an agonistic mode of action toward hERß and, thereby, inducing ER subtype-selective behavior.
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Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Glycine max / Modulateurs sélectifs des récepteurs des oestrogènes / Ptérocarpanes / Phyto-oestrogènes Limites: Humans Langue: En Journal: J Steroid Biochem Mol Biol Sujet du journal: BIOLOGIA MOLECULAR / BIOQUIMICA Année: 2016 Type de document: Article Pays d'affiliation: Pays-Bas

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Glycine max / Modulateurs sélectifs des récepteurs des oestrogènes / Ptérocarpanes / Phyto-oestrogènes Limites: Humans Langue: En Journal: J Steroid Biochem Mol Biol Sujet du journal: BIOLOGIA MOLECULAR / BIOQUIMICA Année: 2016 Type de document: Article Pays d'affiliation: Pays-Bas
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