Structural and functional evidences for the interactions between nuclear hormone receptors and endocrine disruptors at low doses

被引:55
作者
Balaguer, Patrick [1 ,2 ,3 ,4 ]
Delfosse, Vanessa [4 ,5 ,6 ]
Grimaldi, Marina [1 ,2 ,3 ,4 ]
Bourguet, William [4 ,5 ,6 ]
机构
[1] IRCM, F-34298 Montpellier, France
[2] INSERM, U1194, F-34298 Montpellier, France
[3] Inst Reg Canc Montpellier ICM, F-34298 Montpellier, France
[4] Univ Montpellier, F-34090 Montpellier, France
[5] INSERM, U1054, F-34090 Montpellier, France
[6] CNRS, UMR5048, Ctr Biochim Struct, F-34090 Montpellier, France
关键词
Nuclear receptors; Endocrine disruptors; Low doses; PREGNANE-X RECEPTOR; PROLIFERATOR-ACTIVATED RECEPTORS; PPAR-GAMMA; RISK-ASSESSMENT; ESTROGENS; INSIGHTS; LIGANDS; ALPHA; ACID;
D O I
10.1016/j.crvi.2017.08.002
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Endocrine-disrupting chemicals (EDCs) represent a broad class of exogenous substances that cause adverse effects in the endocrine system mainly by interacting with nuclear hormone receptors (NRs). Humans are generally exposed to low doses of pollutants, and current researches aim at deciphering the mechanisms accounting for the health impact of EDCs at environmental concentrations. Our correlative analysis of structural, interaction and cell-based data has revealed a variety of, sometimes unexpected, binding modes, reflecting a wide range of EDC affinities and specificities. Here, we present a few representative examples to illustrate various means by which EDCs achieve high-affinity binding to NRs. These examples include the binding of the mycoestrogen alpha-zearalanol to estrogen receptors, the covalent interaction of organotins with the retinoid X-and peroxisome proliferator-activated receptors, and the cooperative binding of two chemicals to the pregnane X receptor. We also discuss some hypotheses that could further explain low-concentration effects of EDCs with weaker affinity towards NRs. (C) 2017 Published by Elsevier Masson SAS on behalf of Academie des sciences.
引用
收藏
页码:414 / 420
页数:7
相关论文
共 36 条
[1]   PPARγ signaling and metabolism: the good, the bad and the future [J].
Ahmadian, Maryam ;
Suh, Jae Myoung ;
Hah, Nasun ;
Liddle, Christopher ;
Atkins, Annette R. ;
Downes, Michael ;
Evans, Ronald M. .
NATURE MEDICINE, 2013, 19 (05) :557-566
[2]   Triorganotin compounds - ligands for "rexinoid" inducible transcription factors: Biological effects [J].
Brtko, J. ;
Dvorak, Z. .
TOXICOLOGY LETTERS, 2015, 234 (01) :50-58
[3]   GPR30, the Non-Classical Membrane G Protein Related Estrogen Receptor, Is Overexpressed in Human Seminoma and Promotes Seminoma Cell Proliferation [J].
Chevalier, Nicolas ;
Vega, Aurelie ;
Bouskine, Adil ;
Siddeek, Benazir ;
Michiels, Jean-Francois ;
Chevallier, Daniel ;
Fenichel, Patrick .
PLOS ONE, 2012, 7 (04)
[4]   Estrogen receptor null mice: What have we learned and where will they lead us? [J].
Couse, JF ;
Korach, KS .
ENDOCRINE REVIEWS, 1999, 20 (03) :358-417
[5]   Synergistic activation of human pregnane X receptor by binary cocktails of pharmaceutical and environmental compounds [J].
Delfosse, Vanessa ;
Dendele, Beatrice ;
Huet, Tiphaine ;
Grimaldi, Marina ;
Boulahtouf, Abdelhay ;
Gerbal-Chaloin, Sabine ;
Beucher, Bertrand ;
Roecklin, Dominique ;
Muller, Christina ;
Rahmani, Roger ;
Cavailles, Vincent ;
Daujat-Chavanieu, Martine ;
Vivat, Valerie ;
Pascussi, Jean-Marc ;
Balaguer, Patrick ;
Bourguet, William .
NATURE COMMUNICATIONS, 2015, 6
[6]   A structural perspective on nuclear receptors as targets of environmental compounds [J].
Delfosse, Vanessa ;
le Maire, Albane ;
Balaguer, Patrick ;
Bourguet, William .
ACTA PHARMACOLOGICA SINICA, 2015, 36 (01) :88-101
[7]   Structural and Functional Profiling of Environmental Ligands for Estrogen Receptors [J].
Delfosse, Vanessa ;
Grimaldi, Marina ;
Cavailles, Vincent ;
Balaguer, Patrick ;
Bourguet, William .
ENVIRONMENTAL HEALTH PERSPECTIVES, 2014, 122 (12) :1306-1313
[8]   Structural and mechanistic insights into bisphenols action provide guidelines for risk assessment and discovery of bisphenol A substitutes [J].
Delfosse, Vanessa ;
Grimaldi, Marina ;
Pons, Jean-Luc ;
Boulahtouf, Abdelhay ;
le Maire, Albane ;
Cavailles, Vincent ;
Labesse, Gilles ;
Bourguet, William ;
Balaguer, Patrick .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2012, 109 (37) :14930-14935
[9]   17-OxoDHA Is a PPARα/γ Dual Covalent Modifier and Agonist [J].
Egawa, Daichi ;
Itoh, Toshimasa ;
Akiyama, Yui ;
Saito, Tomoko ;
Yamamoto, Keiko .
ACS CHEMICAL BIOLOGY, 2016, 11 (09) :2447-2455
[10]   Evaluation of ligand selectivity using reporter cell lines stably expressing estrogen receptor alpha or beta [J].
Escande, A ;
Pillon, A ;
Servant, N ;
Cravedi, JP ;
Larrea, F ;
Muhn, P ;
Nicolas, JC ;
Cavaillès, V ;
Balaguer, P .
BIOCHEMICAL PHARMACOLOGY, 2006, 71 (10) :1459-1469