Literature DB >> 26655113

Glyceollins and dehydroglyceollins isolated from soybean act as SERMs and ER subtype-selective phytoestrogens.

Milou G M van de Schans1, Jean-Paul Vincken2, Pieter de Waard3, Astrid R M Hamers4, Toine F H Bovee4, Harry Gruppen1.   

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 hERβ) 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 hERβ. 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 hERβ and, thereby, inducing ER subtype-selective behavior.
Copyright © 2015 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  6a,11a-Pterocarpene; 6a-Hydroxy-pterocarpan; Molar extinction coefficient; Prenylation; hER yeast bioassay; hERα-CALUX

Mesh:

Substances:

Year:  2015        PMID: 26655113     DOI: 10.1016/j.jsbmb.2015.11.020

Source DB:  PubMed          Journal:  J Steroid Biochem Mol Biol        ISSN: 0960-0760            Impact factor:   4.292


  7 in total

1.  Structural basis for non-genuine phenolic acceptor substrate specificity of Streptomyces roseochromogenes prenyltransferase CloQ from the ABBA/PT-barrel superfamily.

Authors:  Carla Araya-Cloutier; Bianca Martens; Gijs Schaftenaar; Franziska Leipoldt; Harry Gruppen; Jean-Paul Vincken
Journal:  PLoS One       Date:  2017-03-29       Impact factor: 3.240

2.  Asymmetric one-pot transformation of isoflavones to pterocarpans and its application in phytoalexin synthesis.

Authors:  Philipp Ciesielski; Peter Metz
Journal:  Nat Commun       Date:  2020-06-18       Impact factor: 14.919

3.  Distinct Mechanisms of Biotic and Chemical Elicitors Enable Additive Elicitation of the Anticancer Phytoalexin Glyceollin I.

Authors:  Kelli Farrell; Md Asraful Jahan; Nik Kovinich
Journal:  Molecules       Date:  2017-07-27       Impact factor: 4.411

4.  QSAR-based molecular signatures of prenylated (iso)flavonoids underlying antimicrobial potency against and membrane-disruption in Gram positive and Gram negative bacteria.

Authors:  Carla Araya-Cloutier; Jean-Paul Vincken; Milou G M van de Schans; Jos Hageman; Gijs Schaftenaar; Heidy M W den Besten; Harry Gruppen
Journal:  Sci Rep       Date:  2018-06-18       Impact factor: 4.379

5.  Toward Developing a Yeast Cell Factory for the Production of Prenylated Flavonoids.

Authors:  Mark Levisson; Carla Araya-Cloutier; Wouter J C de Bruijn; Menno van der Heide; José Manuel Salvador López; Jean-Marc Daran; Jean-Paul Vincken; Jules Beekwilder
Journal:  J Agric Food Chem       Date:  2019-05-02       Impact factor: 5.279

6.  Insights into the molecular properties underlying antibacterial activity of prenylated (iso)flavonoids against MRSA.

Authors:  Sylvia Kalli; Carla Araya-Cloutier; Jos Hageman; Jean-Paul Vincken
Journal:  Sci Rep       Date:  2021-07-09       Impact factor: 4.379

Review 7.  The Potential of Phytochemicals in Oral Cancer Prevention and Therapy: A Review of the Evidence.

Authors:  Tzu-Ying Lee; Yu-Hsin Tseng
Journal:  Biomolecules       Date:  2020-08-06
  7 in total

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