메뉴 건너뛰기




Volumn 309, Issue , 2013, Pages 15-22

Structure-dependent activities of hydroxylated polybrominated diphenyl ethers on human estrogen receptor

Author keywords

Estrogen receptor; Ligand binding assay; Molecular docking; MVLN cell transactivation assay; OH PBDEs; Surface plasmon resonance

Indexed keywords

ESTROGEN RECEPTOR; LUCIFERASE; POLYBROMINATED DIPHENYL ETHER;

EID: 84877829614     PISSN: 0300483X     EISSN: 18793185     Source Type: Journal    
DOI: 10.1016/j.tox.2013.04.001     Document Type: Article
Times cited : (42)

References (32)
  • 1
    • 40849102532 scopus 로고    scopus 로고
    • Polybrominated diphenyl ethers (PBDEs) and bioaccumulative hydroxylated PBDE metabolites in young humans from Managua, Nicaragua
    • Athanasiadou M., Cuadra S.N., Marsh G., Bergman Å., Jakobsson K. Polybrominated diphenyl ethers (PBDEs) and bioaccumulative hydroxylated PBDE metabolites in young humans from Managua, Nicaragua. Environ. Health Perspect. 2007, 116:400-408.
    • (2007) Environ. Health Perspect. , vol.116 , pp. 400-408
    • Athanasiadou, M.1    Cuadra, S.N.2    Marsh, G.3    Bergman, Å.4    Jakobsson, K.5
  • 3
    • 33244478590 scopus 로고    scopus 로고
    • Gene expression and estrogen sensitivity in rat uterus after developmental exposure to the polybrominated diphenylether PBDE 99 and PCB
    • Ceccatelli R., Faass O., Schlumpf M., Lichtensteiger W. Gene expression and estrogen sensitivity in rat uterus after developmental exposure to the polybrominated diphenylether PBDE 99 and PCB. Toxicology 2006, 220:104-116.
    • (2006) Toxicology , vol.220 , pp. 104-116
    • Ceccatelli, R.1    Faass, O.2    Schlumpf, M.3    Lichtensteiger, W.4
  • 5
    • 10044220908 scopus 로고    scopus 로고
    • Screening for estrogenicity and anti-estrogenicity: a critical evaluation of an MVLN cell-based transactivation assay
    • Freyberger A., Schmuck G. Screening for estrogenicity and anti-estrogenicity: a critical evaluation of an MVLN cell-based transactivation assay. Toxicol. Lett. 2005, 155:1-13.
    • (2005) Toxicol. Lett. , vol.155 , pp. 1-13
    • Freyberger, A.1    Schmuck, G.2
  • 6
    • 0035805514 scopus 로고    scopus 로고
    • Crystal structure of a mutant hERalpha ligand-binding domain reveals key structural features for the mechanism of partial agonism
    • Gangloff M., Ruff M., Eiler S., Duclaud S., Wurtz J.M., Moras D. Crystal structure of a mutant hERalpha ligand-binding domain reveals key structural features for the mechanism of partial agonism. J. Biol. Chem. 2001, 276:15059-15065.
    • (2001) J. Biol. Chem. , vol.276 , pp. 15059-15065
    • Gangloff, M.1    Ruff, M.2    Eiler, S.3    Duclaud, S.4    Wurtz, J.M.5    Moras, D.6
  • 8
    • 41949131790 scopus 로고    scopus 로고
    • Biotransformation of brominated flame retardants into potentially endocrine-disrupting metabolites, with special attention to 2,2',4,4'-tetrabromodiphenyl ether (BDE-47)
    • Hamers T., Kamstra J.H., Sonneveld E., Murk A.J., Visser T.J., Van Velzen M.J., et al. Biotransformation of brominated flame retardants into potentially endocrine-disrupting metabolites, with special attention to 2,2',4,4'-tetrabromodiphenyl ether (BDE-47). Mol. Nutr. Food Res. 2008, 52:284-298.
    • (2008) Mol. Nutr. Food Res. , vol.52 , pp. 284-298
    • Hamers, T.1    Kamstra, J.H.2    Sonneveld, E.3    Murk, A.J.4    Visser, T.J.5    Van Velzen, M.J.6
  • 9
    • 1242297693 scopus 로고    scopus 로고
    • Polybrominated diphenyl ethers in the environment and in people: a meta-analysis of concentrations
    • Hites R.A. Polybrominated diphenyl ethers in the environment and in people: a meta-analysis of concentrations. Environ. Sci Technol. 2004, 38:945-956.
    • (2004) Environ. Sci Technol. , vol.38 , pp. 945-956
    • Hites, R.A.1
  • 10
    • 79952628793 scopus 로고    scopus 로고
    • Noriyuki Disruption of thyroid hormone receptor-mediated transcription and thyroid hormone-induced Purkinje cell dendrite arborization by polybrominated diphenyl ethers
    • Ibhazehiebo K., Iwasaki T., Kimura-Kuroda J., Miyazaki W., Shimokawa N.a.K., Noriyuki Disruption of thyroid hormone receptor-mediated transcription and thyroid hormone-induced Purkinje cell dendrite arborization by polybrominated diphenyl ethers. Environ. Health Perspect. 2011, 119:168-175.
    • (2011) Environ. Health Perspect. , vol.119 , pp. 168-175
    • Ibhazehiebo, K.1    Iwasaki, T.2    Kimura-Kuroda, J.3    Miyazaki, W.4    Shimokawa, N.5
  • 11
    • 0034141443 scopus 로고    scopus 로고
    • Biosensor analysis of drug-target interactions: direct and competitive binding assays for investigation of interactions between thrombin and thrombin inhibitors
    • Karlsson R., Kullman-Magnusson M., Hamalainen M.D., Remaeus A., Andersson K., Borg P., et al. Biosensor analysis of drug-target interactions: direct and competitive binding assays for investigation of interactions between thrombin and thrombin inhibitors. Anal. Biochem. 2000, 278:1-13.
    • (2000) Anal. Biochem. , vol.278 , pp. 1-13
    • Karlsson, R.1    Kullman-Magnusson, M.2    Hamalainen, M.D.3    Remaeus, A.4    Andersson, K.5    Borg, P.6
  • 12
    • 54249095556 scopus 로고    scopus 로고
    • Affinity for thyroid hormone and estrogen receptors of hydroxylated polybrominated diphenyl ethers
    • Kitamura S., Schinohara S., Iwase E., Sugihara K., Uramaru N., Shigematsu H., et al. Affinity for thyroid hormone and estrogen receptors of hydroxylated polybrominated diphenyl ethers. J. Health Sci. 2008, 54:607-614.
    • (2008) J. Health Sci. , vol.54 , pp. 607-614
    • Kitamura, S.1    Schinohara, S.2    Iwase, E.3    Sugihara, K.4    Uramaru, N.5    Shigematsu, H.6
  • 13
    • 69249109660 scopus 로고    scopus 로고
    • Nuclear hormone receptor activity of polybrominated diphenyl ethers and their hydroxylated and methoxylated metabolites in transactivation assays using Chinese hamster ovary cells
    • Kojima H., Takeuchi S., Uramaru N., Sugihara K., Yoshida T., Kitamura S. Nuclear hormone receptor activity of polybrominated diphenyl ethers and their hydroxylated and methoxylated metabolites in transactivation assays using Chinese hamster ovary cells. Environ. Health Perspect. 2009, 117:1210-1218.
    • (2009) Environ. Health Perspect. , vol.117 , pp. 1210-1218
    • Kojima, H.1    Takeuchi, S.2    Uramaru, N.3    Sugihara, K.4    Yoshida, T.5    Kitamura, S.6
  • 15
    • 0033051859 scopus 로고    scopus 로고
    • EM-652 (SCH 57068), a third genenration SERM acting as pure antiestrogen in the mammary gland and endometrium
    • Labrie F., Labrie C., Belanger A., Simard J., Gauthier S., Luu-The V., et al. EM-652 (SCH 57068), a third genenration SERM acting as pure antiestrogen in the mammary gland and endometrium. J. Steroid Biochem. Mol. Biol. 1999, 69:51-84.
    • (1999) J. Steroid Biochem. Mol. Biol. , vol.69 , pp. 51-84
    • Labrie, F.1    Labrie, C.2    Belanger, A.3    Simard, J.4    Gauthier, S.5    Luu-The, V.6
  • 16
    • 32044467384 scopus 로고    scopus 로고
    • Effects of developmental exposure to 2,2',4,4',5-pentabromodiphenyl ether (PBDE-99) on sex steroids, sexual development, and sexually dimorphic behavior in rats
    • Lilienthal H., Hack A., Roth-Härer A., Grande S.W., Talsness C.E. Effects of developmental exposure to 2,2',4,4',5-pentabromodiphenyl ether (PBDE-99) on sex steroids, sexual development, and sexually dimorphic behavior in rats. Environ. Health Perspect. 2006, 114:194-201.
    • (2006) Environ. Health Perspect. , vol.114 , pp. 194-201
    • Lilienthal, H.1    Hack, A.2    Roth-Härer, A.3    Grande, S.W.4    Talsness, C.E.5
  • 17
    • 79960381371 scopus 로고    scopus 로고
    • In vitro profiling of endocrine disrupting potency of 2,2',4,4'-tetrabromodiphenyl ether (BDE47) and related hydroxylated analogs (HO-PBDEs)
    • Liu H., Hu W., Sun H., Shen O., Wang X., Lam M.H., et al. In vitro profiling of endocrine disrupting potency of 2,2',4,4'-tetrabromodiphenyl ether (BDE47) and related hydroxylated analogs (HO-PBDEs). Mar. Pollut. Bull. 2011, 63:287-296.
    • (2011) Mar. Pollut. Bull. , vol.63 , pp. 287-296
    • Liu, H.1    Hu, W.2    Sun, H.3    Shen, O.4    Wang, X.5    Lam, M.H.6
  • 19
    • 0035025255 scopus 로고    scopus 로고
    • In vitro estrogenicity of polybrominated diphenyl ethers, hydroxylated PBDEs, and polybrominated bisphenol A compounds
    • Meerts I.A.T.M., Letcher R.J., Hoving S., Marsh G., Bergman A., Lemmen J.G., et al. In vitro estrogenicity of polybrominated diphenyl ethers, hydroxylated PBDEs, and polybrominated bisphenol A compounds. Environ. Health Perspect. 2001, 109:399-407.
    • (2001) Environ. Health Perspect. , vol.109 , pp. 399-407
    • Meerts, I.A.T.M.1    Letcher, R.J.2    Hoving, S.3    Marsh, G.4    Bergman, A.5    Lemmen, J.G.6
  • 20
    • 0033607458 scopus 로고    scopus 로고
    • Analysis of polybrominated diphenyl ethers in Swedish human milk. A Time-Related Trend Study, 1972-1997
    • Meironyte D., Noren K., Bergman A. Analysis of polybrominated diphenyl ethers in Swedish human milk. A Time-Related Trend Study, 1972-1997. J. Toxicol. Environ. Health, Part A 1999, 58:329-341.
    • (1999) J. Toxicol. Environ. Health, Part A , vol.58 , pp. 329-341
    • Meironyte, D.1    Noren, K.2    Bergman, A.3
  • 21
    • 55949090982 scopus 로고    scopus 로고
    • Hydroxylated metabolites of the polybrominated diphenyl ether mixture DE-71 are weak estrogen receptor-alpha ligands
    • Mercado-Feliciano M., Bigsby R.M. Hydroxylated metabolites of the polybrominated diphenyl ether mixture DE-71 are weak estrogen receptor-alpha ligands. Environ. Health Perspect. 2008, 116:1315-1321.
    • (2008) Environ. Health Perspect. , vol.116 , pp. 1315-1321
    • Mercado-Feliciano, M.1    Bigsby, R.M.2
  • 23
    • 0025187484 scopus 로고
    • A new cellular model of response to estrogens: a bioluminescent test to characterize (anti)estrogen molecules
    • Pons M., Gagne D., Nicolas J., Claude Mehtali M. A new cellular model of response to estrogens: a bioluminescent test to characterize (anti)estrogen molecules. BioTechniques 1990, 9:450-459.
    • (1990) BioTechniques , vol.9 , pp. 450-459
    • Pons, M.1    Gagne, D.2    Nicolas, J.3    Claude Mehtali, M.4
  • 24
    • 60749103207 scopus 로고    scopus 로고
    • Hydroxylated metabolites of polybrominated diphenyl ethers in human blood samples from the United States
    • Qiu X., Bisby R.M., Hites R.A. Hydroxylated metabolites of polybrominated diphenyl ethers in human blood samples from the United States. Environ. Health Perspect. 2009, 117:93-98.
    • (2009) Environ. Health Perspect. , vol.117 , pp. 93-98
    • Qiu, X.1    Bisby, R.M.2    Hites, R.A.3
  • 26
    • 14844324970 scopus 로고    scopus 로고
    • Polybrominated diphenyl ethers (PBDEs) in U.S. computers and domestic carpet vacuuming: possible sources of human exposure
    • Schecter A., Papke O., Joseph J.E., Tung K.C. Polybrominated diphenyl ethers (PBDEs) in U.S. computers and domestic carpet vacuuming: possible sources of human exposure. J. Toxicol. Environ. Health A 2005, 68:501-513.
    • (2005) J. Toxicol. Environ. Health A , vol.68 , pp. 501-513
    • Schecter, A.1    Papke, O.2    Joseph, J.E.3    Tung, K.C.4
  • 27
    • 0036223180 scopus 로고    scopus 로고
    • PBDEs in the San Francisco Bay Area: measurements in harbor seal blubber and human breast adipose tissue
    • She J.W., Petreas M., Winkler J., Visita P., McKinney M., Kopec D. PBDEs in the San Francisco Bay Area: measurements in harbor seal blubber and human breast adipose tissue. Chemosphere 2002, 46:697-707.
    • (2002) Chemosphere , vol.46 , pp. 697-707
    • She, J.W.1    Petreas, M.2    Winkler, J.3    Visita, P.4    McKinney, M.5    Kopec, D.6
  • 28
    • 0032446607 scopus 로고    scopus 로고
    • The structural basis of estrogen receptor/coactivator recognition and the antagonism of this interaction by tamoxifen
    • Shiau A.K., Barstad D., Loria P.M., Cheng L., Kushner P.J., Agard D.A., et al. The structural basis of estrogen receptor/coactivator recognition and the antagonism of this interaction by tamoxifen. Cell 1998, 95:927-937.
    • (1998) Cell , vol.95 , pp. 927-937
    • Shiau, A.K.1    Barstad, D.2    Loria, P.M.3    Cheng, L.4    Kushner, P.J.5    Agard, D.A.6
  • 29
    • 2442433767 scopus 로고    scopus 로고
    • Patterson Retrospective time-trend study of polybrominated diphenyl ether and polybrominated and polychlorinated biphenyl levels in human serum from the United States
    • Sjodin A., Jones R.S., Focant J.-F., Lapeza C., Wang R.Y., McGahee E.M., Zhang Y., Turner W.E., Slazyk B., Needham L.L., Patterson Retrospective time-trend study of polybrominated diphenyl ether and polybrominated and polychlorinated biphenyl levels in human serum from the United States. Environ. Health Perspect. 2004, 112:654-658.
    • (2004) Environ. Health Perspect. , vol.112 , pp. 654-658
    • Sjodin, A.1    Jones, R.S.2    Focant, J.-F.3    Lapeza, C.4    Wang, R.Y.5    McGahee, E.M.6    Zhang, Y.7    Turner, W.E.8    Slazyk, B.9    Needham, L.L.10
  • 30
    • 0004752110 scopus 로고    scopus 로고
    • Novel ligands that function as selective estrogens or antiestrogens for estrogen receptor-α or estrogen receptor-β
    • Sun J., Meyers M.J., Fink B.E., Rajendran R., Katzenellenbogen J.A., Katzenellenbogen B.S. Novel ligands that function as selective estrogens or antiestrogens for estrogen receptor-α or estrogen receptor-β. Endocrinology 1998, 140:800-804.
    • (1998) Endocrinology , vol.140 , pp. 800-804
    • Sun, J.1    Meyers, M.J.2    Fink, B.E.3    Rajendran, R.4    Katzenellenbogen, J.A.5    Katzenellenbogen, B.S.6
  • 31
    • 84855248697 scopus 로고    scopus 로고
    • The in vitro estrogenic activities of polyfluorinated iodine alkanes
    • Wang C., Wang T., Liu W., Ruan T., Zhou Q., Liu J., et al. The in vitro estrogenic activities of polyfluorinated iodine alkanes. Environ. Health Perspect. 2012, 120:119-125.
    • (2012) Environ. Health Perspect. , vol.120 , pp. 119-125
    • Wang, C.1    Wang, T.2    Liu, W.3    Ruan, T.4    Zhou, Q.5    Liu, J.6
  • 32
    • 79960362344 scopus 로고    scopus 로고
    • Polybrominated diphenyl ethers and their hydroxylated/methoxylated analogs: environmental sources, metabolic relationships, and relative toxicities
    • Wiseman S.B., Wan Y., Chang H., Zhang X., Hecker M., Jones P.D., et al. Polybrominated diphenyl ethers and their hydroxylated/methoxylated analogs: environmental sources, metabolic relationships, and relative toxicities. Mar. Pollut. Bull. 2011, 63:179-188.
    • (2011) Mar. Pollut. Bull. , vol.63 , pp. 179-188
    • Wiseman, S.B.1    Wan, Y.2    Chang, H.3    Zhang, X.4    Hecker, M.5    Jones, P.D.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.