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Identification and pharmacological characterization of cholesterol-5,6-epoxide hydrolase as a target for tamoxifen and AEBS ligands.

Philippe de Medina 1, 2 Michael Paillasse 1, 2 Grégory Segala 2 Marc Poirot 2 Sandrine Silvente-Poirot 2
2 Departement /u563 : Oncogenèse, Signalisation et Innovation thérapeutique
CPTP - Centre de Physiopathologie Toulouse Purpan ex IFR 30 et IFR 150, Institut Claudius Regaud
Abstract : The microsomal antiestrogen binding site (AEBS) is a high-affinity target for the antitumor drug tamoxifen and its cognate ligands that mediate breast cancer cell differentiation and apoptosis. The AEBS, a hetero-oligomeric complex composed of 3beta-hydroxysterol-Delta8-Delta7-isomerase (D8D7I) and 3beta-hydroxysterol-Delta7-reductase (DHCR7), binds different structural classes of ligands, including ring B oxysterols. These oxysterols are inhibitors of cholesterol-5,6-epoxide hydrolase (ChEH), a microsomal epoxide hydrolase that has yet to be molecularly identified. We hypothesized that the AEBS and ChEH might be related entities. We show that the substrates of ChEH, cholestan-5alpha,6alpha-epoxy-3beta-ol (alpha-CE) and cholestan-5beta,6beta-epoxy-3beta-ol (beta-CE), and its product, cholestane-3beta,5alpha,6beta-triol (CT), are competitive ligands of tamoxifen binding to the AEBS. Conversely, we show that each AEBS ligand is an inhibitor of ChEH activity, and that there is a positive correlation between these ligands' affinity for the AEBS and their potency to inhibit ChEH (r2=0.95; n=39; P<0.0001). The single expression of D8D7I or DHCR7 in COS-7 cells slightly increased ChEH activity (1.8- and 2.6-fold), whereas their coexpression fully reconstituted ChEH, suggesting that the formation of a dimer is required for ChEH activity. Similarly, the single knockdown of D8D7I or DHCR7 using siRNA partially inhibited ChEH in MCF-7 cells, whereas the knockdown of both D8D7I and DHCR7 abolished ChEH activity by 92%. Taken together, our findings strongly suggest that the AEBS carries out ChEH activity and establish that ChEH is a new target for drugs of clinical interest, polyunsaturated fatty acids and ring B oxysterols.
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https://www.hal.inserm.fr/inserm-00519159
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Submitted on : Saturday, September 18, 2010 - 3:31:49 PM
Last modification on : Monday, June 29, 2020 - 2:18:02 PM

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Philippe de Medina, Michael Paillasse, Grégory Segala, Marc Poirot, Sandrine Silvente-Poirot. Identification and pharmacological characterization of cholesterol-5,6-epoxide hydrolase as a target for tamoxifen and AEBS ligands.. Proceedings of the National Academy of Sciences of the United States of America , National Academy of Sciences, 2010, 107 (30), pp.13520-5. ⟨10.1073/pnas.1002922107⟩. ⟨inserm-00519159⟩

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