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Ligand binding and activation of the Ah receptor
Abstract
The Ah receptor (AhR) is a ligand-dependent transcription factor that can be activated by structurally diverse synthetic and naturally-occurring chemicals. Although a significant amount of information is available with respect to the planar aromatic hydrocarbon AhR ligands, the actual spectrum of chemicals that can bind to and activate the AhR is only now being elucidated. In addition, the lack of information regarding the actual three-dimensional structure of the AhR ligand binding domain (LBD) has hindered detailed analysis of the molecular mechanisms by which these ligands bind to and active AhR signal transduction. In this review we describe the current state of knowledge with respect to naturally occurring AhR ligands and present and discuss the first theoretical model of the AhR LBD based on crystal structures of homologous PAS family members.
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“While the AhR can bind and be activated by a large number of structurally diverse chemicals (4-6), the highest affinity ligands include halogenated aromatic hydrocarbons (HAHs), such as 2,3,7,8tetrachlorodibenzop -dioxin (TCDD, dioxin), and polycyclic aromatic hydrocarbons (PAHs), both widespread classes of environmental contaminants (4,7).”
From Structural and Functional Characterization of the Aryl Hydrocarbon Receptor Ligand Binding Domain by Homology Modeling and Mutational Analysis (2007) · cites this paper as [6]
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Cites
Berman, H. M. (2000) · Nucleic Acids Research · doi:10.1093/nar/28.1.235 · Cited by 40,196
Poland, A., & Knutson, J. C. (1982) · Annual Review of Pharmacology and Toxicology · doi:10.1146/annurev.pa.22.040182.002505 · Cited by 2,515
Safe, S. (1990) · Critical Reviews in Toxicology · doi:10.3109/10408449009089873 · Cited by 1,871
Safe, S. H. (1994) · Critical Reviews in Toxicology · doi:10.3109/10408449409049308 · Cited by 1,760
The Aryl Hydrocarbon Receptor Complex
Hankinson, O. (1995) · Annual Review of Pharmacology and Toxicology · doi:10.1146/annurev.pa.35.040195.001515 · Cited by 1,649 · cited 2×
“Formation of the AhR:Arnt heterodimer converts the complex into its high affinity DNA binding form [1,19] and binding of the complex to its specific DNA recognition site, the dioxin responsive element (DRE), upstream of the CYP1A1 gene leads to chromatin and nucleosome disruption, increased promoter accessibility and…”
BackgroundPAS Domains: Internal Sensors of Oxygen, Redox Potential, and Light
Taylor, B. L., & Zhulin, I. B. (1999) · Microbiology and Molecular Biology Reviews · doi:10.1128/mmbr.63.2.479-506.1999 · Cited by 1,632
INDUCTION OF CYTOCHROME P4501A1
Whitlock, J. P. (1999) · The Annual Review of Pharmacology and Toxicology · doi:10.1146/annurev.pharmtox.39.1.103 · Cited by 1,136
Immune System Impairment and Hepatic Fibrosis in Mice Lacking the Dioxin-Binding Ah Receptor
Fernandez-Salguero, P., Pineau, T., Hilbert, D. M., McPhail, T., Lee, S. S. T., Kimura, S., Nebert, D. W., Rudikoff, S., Ward, J. M., & Gonzalez, F. J. (1995) · Science · doi:10.1126/science.7732381 · Cited by 1,075
The PAS Superfamily: Sensors of Environmental and Developmental Signals
Gu, Y.-Z., Hogenesch, J. B., & Bradfield, C. A. (2000) · The Annual Review of Pharmacology and Toxicology · doi:10.1146/annurev.pharmtox.40.1.519 · Cited by 1,044
Schmidt, J. V., Su, G. H., Reddy, J. K., Simon, M. C., & Bradfield, C. A. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.13.6731 · Cited by 902
AH RECEPTOR SIGNALING PATHWAYS
Schmidt, J. V., & Bradfield, C. A. (1996) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.12.1.55 · Cited by 899
The eicosanoids and their biochemical mechanisms of action
Smith, W. L. (1989) · Biochemical Journal · doi:10.1042/bj2590315 · Cited by 876
Safe, S. H. (1986) · The Annual Review of Pharmacology and Toxicology · doi:10.1146/annurev.pa.26.040186.002103 · Cited by 710
Bjeldanes, L. F., Kim, J. Y., Grose, K. R., Bartholomew, J. C., & Bradfield, C. A. (1991) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.88.21.9543 · Cited by 596
Aryl Hydrocarbon Receptor-Mediated Signal Transduction
Rowlands, J. C., & Gustafsson, J.-Å. (1997) · Critical Reviews in Toxicology · doi:10.3109/10408449709021615 · Cited by 490
Crosson, S., & Moffat, K. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.051520298 · Cited by 473
Denison, M. S., Fisher, J. M., & Whitlock, J. P. (1988) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)77819-3 · Cited by 451
Self-citationCrystal Structure and Functional Analysis of the HERG Potassium Channel N Terminus
Morais-Cabral, J. H., Lee, A., Cohen, S. L., Chait, B. T., Li, M., & MacKinnon, R. (1998) · Cell · doi:10.1016/s0092-8674(00)81635-9 · Cited by 436
Inhibition of polycyclic aromatic hydrocarbon-induced neoplasia by naturally occurring indoles.
Wattenberg, L. W., & Loub, W. D. (1978) · PubMed · Cited by 432
Carver, L. A., & Bradfield, C. (1997) · Journal of Biological Chemistry · doi:10.1074/jbc.272.17.11452 · Cited by 428
Ma, Q., & Whitlock, J. P. (1997) · Journal of Biological Chemistry · doi:10.1074/jbc.272.14.8878 · Cited by 426
Hardell, L., Eriksson, M., Axelson, O., & Hoar Zahm, S. (1994) · Springer eBooks · doi:10.1007/978-1-4899-1462-0 · Cited by 417
Indirubin and Indigo Are Potent Aryl Hydrocarbon Receptor Ligands Present in Human Urine
Adachi, J., Mori, Y., Matsui, S., Takigami, H., Fujino, J., Kitagawa, H., Miller, C. A., Kato, T., Saeki, K., & Matsuda, T. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.c100238200 · Cited by 407
Structure of a Protein Photocycle Intermediate by Millisecond Time-Resolved Crystallography
Genick, U. K., Borgstahl, G. E. O., Ng, K., Ren, Z. M., Pradervand, C., Burke, P. M., Šrajer, V., Teng, T.-Y., Schildkamp, W., McRee, D. E., et al. (1997) · Science · doi:10.1126/science.275.5305.1471 · Cited by 407
Garrison, P. M. (1996) · Fundamental and Applied Toxicology · doi:10.1006/faat.1996.0056 · Cited by 406
Meyer, B., Pray-Grant, M. G., Heuvel, J. P. V., & Perdew, G. (1998) · Molecular and Cellular Biology · doi:10.1128/mcb.18.2.978 · Cited by 390
Lahvis, G. P., Lindell, S. L., Thomas, R. S., McCuskey, R. S., Murphy, C., Glover, E., Bentz, M., Southard, J., & Bradfield, C. A. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.190256997 · Cited by 377
The aryl hydrocarbon receptor: A comparative perspective
Hahn, M. E. (1998) · Comparative Biochemistry and Physiology Part C Pharmacology Toxicology and Endocrinology · doi:10.1016/s0742-8413(98)10028-2 · Cited by 369
Rannug, A., Rannug, U., Rosenkranz, H. S., Winqvist, L., Westerholm, R. N., Agurell, E., & Grafström, A.-K. (1987) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)47743-5 · Cited by 357
Safe, S. H. (1995) · Pharmacology & Therapeutics · doi:10.1016/0163-7258(95)00017-b · Cited by 357
Structure of a biological oxygen sensor: A new mechanism for heme-driven signal transduction
Gong, W., Hao, B., Mansy, S. S., Gonzalez, G., Gilles‐Gonzalez, M., & Chan, M. K. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.26.15177 · Cited by 356
Activation of the Ah Receptor by Tryptophan and Tryptophan Metabolites
Heath‐Pagliuso, S., Rogers, W. J., Tullis, K. M., Seidel, S. D., Cenijn, P. H., Brouwer, A., & Denison, M. S. (1998) · Biochemistry · doi:10.1021/bi980087p · Cited by 331
Self-citationDioxin binding activities of polymorphic forms of mouse and human arylhydrocarbon receptors.
Ema, M., Ohe, N., Suzuki, M., Mimura, J., Sogawa, K., Ikawa, S., & Fujii-Kuriyama, Y. (1994) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)46990-6 · Cited by 329
Activation of the Ah Receptor Signal Transduction Pathway by Bilirubin and Biliverdin
Phelan, D., Winter, G. M., Rogers, W. J., Lam, J., & Denison, M. S. (1998) · Archives of Biochemistry and Biophysics · doi:10.1006/abbi.1998.0814 · Cited by 318
Self-citationPollenz, R. S., Sattler, C. A., & Poland, A. (1994) · Molecular Pharmacology · doi:10.1016/s0026-895x(25)10014-x · Cited by 315
Serhan, C. N., & Sheppard, K.-A. (1990) · Journal of Clinical Investigation · doi:10.1172/jci114503 · Cited by 314
Analysis of the four alleles of the murine aryl hydrocarbon receptor
Poland, A., Palen, D., & Glover, E. (1994) · Molecular Pharmacology · doi:10.1016/s0026-895x(25)09833-5 · Cited by 303
Kazlauskas, A., Poellinger, L., & Pongratz, I. (1999) · Journal of Biological Chemistry · doi:10.1074/jbc.274.19.13519 · Cited by 302
Nuclear Localization and Export Signals of the Human Aryl Hydrocarbon Receptor
Ikuta, T., Eguchi, H., Tachibana, T., Yoneda, Y., & Kawajiri, K. (1998) · Journal of Biological Chemistry · doi:10.1074/jbc.273.5.2895 · Cited by 287
Hahn, M. E., Karchner, S. I., Shapiro, M. A., & Perera, S. A. (1997) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.94.25.13743 · Cited by 278
Ma, Q., & Whitlock, J. P. (1996) · Molecular and Cellular Biology · doi:10.1128/mcb.16.5.2144 · Cited by 273
Lipoxin A4: A New Class of Ligand for the Ah Receptor
Schaldach, C., Riby, J. E., & Bjeldanes, L. F. (1999) · Biochemistry · doi:10.1021/bi982861e · Cited by 272
A cavity-containing mutant of T4 lysozyme is stabilized by buried benzene
Sauer-Eriksson, A. E., Baase, W. A., Wozniak, J. A., & Matthews, B. W. (1992) · Nature · doi:10.1038/355371a0 · Cited by 266
Denison, M. S., & Heath-Pagliuso, S. (1998) · Bulletin of Environmental Contamination and Toxicology · doi:10.1007/pl00002973 · Cited by 258
Self-citationSinal, C. J., & Bend, J. R. (1997) · Molecular Pharmacology · doi:10.1124/mol.52.4.590 · Cited by 256
Induction of cytochrome P4501A1: a model for analyzing mammalian gene transcription
Whitlock, J. P., Okino, S. T., Dong, U., Ko, H. P., Katzenberg, R. H., Ma, Q., & Li, H. (1996) · The FASEB Journal · doi:10.1096/fasebj.10.8.8666157 · Cited by 248
Pongratz, I., MASON, G. G. F., & Poellinger, L. (1992) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)42274-0 · Cited by 246
Constitutive Activation of the Aromatic Hydrocarbon Receptor
Chang, C., & Puga, A. (1998) · Molecular and Cellular Biology · doi:10.1128/mcb.18.1.525 · Cited by 245
Ciolino, H. P., Daschner, P. J., Wang, T. T. Y., & Yeh, G. C. (1998) · Biochemical Pharmacology · doi:10.1016/s0006-2952(98)00143-9 · Cited by 241
Ma, Q. (2001) · Current Drug Metabolism · doi:10.2174/1389200013338603 · Cited by 232
Pellequer, J., Wager‐Smith, K., Kay, S. A., & Getzoff, E. D. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.11.5884 · Cited by 231
Protein-DNA Interactions at Recognition Sites for the Dioxin-Ah Receptor Complex
Denison, M. S., Fisher, J. M., & Whitlock, J. P. (1989) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)84730-0 · Cited by 216
Self-citationProbst, M. R., Reisz-Porszasz, S., Agbunag, R. V., Ong, M. S., & Hankinson, O. (1993) · Molecular Pharmacology · doi:10.1016/s0026-895x(25)13218-5 · Cited by 214
Structure elucidation of two tryptophan-derived, high affinity Ah receptor ligands
Rannug, U., Rannug, A., Sjöberg, U., Li, H., Westerholm, R. N., & Bergman, J. (1995) · Chemistry & Biology · doi:10.1016/1074-5521(95)90090-x · Cited by 213
The hsp90 Chaperone Complex Regulates Intracellular Localization of the Dioxin Receptor
Kazlauskas, A., Sundström, S., Poellinger, L., & Pongratz, I. (2001) · Molecular and Cellular Biology · doi:10.1128/mcb.21.7.2594-2607.2001 · Cited by 202
Morton, A., & Matthews, B. W. (1995) · Biochemistry · doi:10.1021/bi00027a007 · Cited by 194
Aarts, J. M. M. J. G., Denison, M. S., Cox, M. A., Schalk, M. A. C., Garrison, P. M., Tullis, K., de Haan, L. H. J., & Brouwer, A. (1995) · European Journal of Pharmacology: Environmental Toxicology and Pharmacology · doi:10.1016/0926-6917(95)90067-5 · Cited by 181
Self-citationCoumailleau, P., Poellinger, L., Gustafsson, J.-Å., & Whitelaw, M. L. (1995) · Journal of Biological Chemistry · doi:10.1074/jbc.270.42.25291 · Cited by 172 · cited 1×
“Full ligand binding activity and specificity of the mouse AhR is reported to be contained within a small fragment (residues 230!/421, 24% of the total AhR protein [120]) and several naturally occurring mutations within this region alter AhR ligand binding affinity [121,122].”
BackgroundWeiß, C., Kolluri, S. K., Kiefer, F., & Göttlicher, M. (1996) · Experimental Cell Research · doi:10.1006/excr.1996.0214 · Cited by 169
Denison, M. S., Vella, L. M., & Okey, A. B. (1986) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(17)35611-9 · Cited by 168
Self-citationWhitelaw, M., Göttlicher, M., Gustafsson, J.-Å., & Poellinger, L. (1993) · EMBO Journal · doi:10.1002/j.1460-2075.1993.tb06101.x · Cited by 157
Hahn, M. E., Poland, A., Glover, E., & Stegeman, J. J. (1994) · Archives of Biochemistry and Biophysics · doi:10.1006/abbi.1994.1160 · Cited by 156
ahr null alleles: distinctive or different?
Lahvis, G. P., & Bradfield, C. A. (1998) · Biochemical Pharmacology · doi:10.1016/s0006-2952(98)00134-8 · Cited by 152
The 90-kDa heat shock protein is essential for Ah receptor signaling in a yeast expression system.
Carver, L. A., Jackiw, V., & Bradfield, C. (1994) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)43782-9 · Cited by 151
Waller, C. L., & McKinney, J. D. (1995) · Chemical Research in Toxicology · doi:10.1021/tx00048a005 · Cited by 150
Expression of the Human Aryl Hydrocarbon Receptor Complex in Yeast
Miller, C. A. (1997) · Journal of Biological Chemistry · doi:10.1074/jbc.272.52.32824 · Cited by 146
Activation of the Ah Receptor Signaling Pathway by Prostaglandins
Seidel, S. D., Winters, G. M., Rogers, W. J., Ziccardi, M. H., Li, V., Keser, B., & Denison, M. S. (2001) · Journal of Biochemical and Molecular Toxicology · doi:10.1002/jbt.16 · Cited by 144
Self-citationGradelet, S., Astorg, P. O., Leclerc, J., Chevalier, J., Vernevaut, M. F., & Siess, M. H. (1996) · Xenobiotica · doi:10.3109/00498259609046688 · Cited by 142
Ciolino, H. P., Wang, T. T. Y., & Yeh, G. C. (1998) · PubMed · Cited by 138
Omeprazole, an inducer of human CYP1A1 and 1A2, is not a ligand for the Ah receptor
Daujat‐Chavanieu, M., Peryt, B., Lesca, P., Fourtanier, G., Domergue, J., & Maurel, P. (1992) · Biochemical and Biophysical Research Communications · doi:10.1016/0006-291x(92)91130-i · Cited by 131
Antonsson, C., Whitelaw, M., McGuire, J., Gustafsson, J.-Å., & Poellinger, L. (1995) · Molecular and Cellular Biology · doi:10.1128/mcb.15.2.756 · Cited by 129
Heat shock protein hsp90 regulates dioxin receptor function in vivo.
Whitelaw, M., McGuire, J., Picard, D., Gustafsson, J.-Å., & Poellinger, L. (1995) · Proceedings of the National Academy of Sciences of the United States of America · doi:10.1073/pnas.92.10.4437 · Cited by 129
Puga, A., Hoffer, A., Zhou, S., Bohm, J. M., Leikauf, G. D., & Shertzer, H. G. (1997) · Biochemical Pharmacology · doi:10.1016/s0006-2952(97)00417-6 · Cited by 122
Miller, C. A. (1999) · Toxicology and Applied Pharmacology · doi:10.1006/taap.1999.8769 · Cited by 114
Nagy, S. R. (2002) · Toxicological Sciences · doi:10.1093/toxsci/65.2.200 · Cited by 114
Self-citationHord, N. G., & Perdew, G. H. (1994) · Molecular Pharmacology · doi:10.1016/s0026-895x(25)09792-5 · Cited by 111
Wei, Y., Bergander, L. V., Rannug, U., & Rannug, A. (2000) · Archives of Biochemistry and Biophysics · doi:10.1006/abbi.2000.2037 · Cited by 110
Access of ligands to cavities within the core of a protein is rapid
Feher, V. A., Baldwin, E. P., & Dahlquist, F. W. (1996) · Nature Structural & Molecular Biology · doi:10.1038/nsb0696-516 · Cited by 110
Self-citationGillner, M., Bergman, J., Cambillau, C., Alexandersson, M., Fernström, B., & Gustafsson, J. (1993) · Molecular Pharmacology · doi:10.1016/s0026-895x(25)13174-x · Cited by 110
Seidel, S. D. (2000) · Toxicological Sciences · doi:10.1093/toxsci/55.1.107 · Cited by 108
Cytochrome P450IA1 is rapidly induced in normal human keratinocytes in the absence of xenobiotics.
Sadek, C. M., & Allen‐Hoffmann, B. L. (1994) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(17)33974-1 · Cited by 106
Ah Receptor in Embryonic Mouse Palate and Effects of TCDD on Receptor Expression
Abbott, B. D., Perdew, G. H., & Birnbaum, L. S. (1994) · Toxicology and Applied Pharmacology · doi:10.1006/taap.1994.1085 · Cited by 103
Definition of a Dioxin Receptor Mutant That Is a Constitutive Activator of Transcription
McGuire, J., Okamoto, K., Whitelaw, M. L., Tanaka, H., & Poellinger, L. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m105607200 · Cited by 102 · cited 1×
“Deletion of residues 287!/421 results in a ligand-independent constitutively active AhR demonstrating the role of the AhR LBD/hsp90 complex in regulating AhR functionality [123].”
BackgroundSingh, S. S., Hord, N. G., & Perdew, G. H. (1996) · Archives of Biochemistry and Biophysics · doi:10.1006/abbi.1996.0190 · Cited by 100
Holmes, J., & Pollenz, R. S. (1997) · Molecular Pharmacology · doi:10.1124/mol.52.2.202 · Cited by 100
Gradelet, S., Leclerc, J., Siess, M. H., & Astorg, P. O. (1996) · Xenobiotica · doi:10.3109/00498259609052493 · Cited by 100
Abnet, C. C., Tanguay, R. L., Heideman, W., & Peterson, R. E. (1999) · Toxicology and Applied Pharmacology · doi:10.1006/taap.1999.8719 · Cited by 96
Toxicology of Dioxins and Related Chemicals
DeVito, M. J., & Birnbaum, L. S. (1994) · Springer eBooks · doi:10.1007/978-1-4899-1462-0_5 · Cited by 96
UV-induced CYP1A1 gene expression in human cells is mediated by tryptophan
Wei, Y., Rannug, U., & Rannug, A. (1999) · Chemico-Biological Interactions · doi:10.1016/s0009-2797(98)00118-5 · Cited by 93
Phototropins: A New Family of Flavin-Binding Blue Light Receptors in Plants
Briggs, W. R., Christie, J. M., & Salomon, M. (2001) · Antioxidants and Redox Signaling · doi:10.1089/15230860152664975 · Cited by 92
Sadek, C. M., & Allen‐Hoffmann, B. L. (1994) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)31723-x · Cited by 90
Nucleocytoplasmic Shuttling of the Aryl Hydrocarbon Receptor
Ikuta, T., Tachibana, T., Watanabe, J. A., Yoshida, M., Yoneda, Y., & Kawajiri, K. (2000) · The Journal of Biochemistry · doi:10.1093/oxfordjournals.jbchem.a022633 · Cited by 90
Ultraviolet Photoproducts of Tryptophan Can Act as Dioxin Agonists
Helferich, W. G., & Denison, M. S. (1991) · Molecular Pharmacology · doi:10.1016/s0026-895x(25)15383-2 · Cited by 88
Self-citationYannai, S., Day, A. J., Williamson, G., & Rhodes, M. J. C. (1998) · Food and Chemical Toxicology · doi:10.1016/s0278-6915(98)00022-2 · Cited by 86
Pettitt, T. R., Rowley, A. F., Barrow, S. E., Mallet, A. I., & Secombes, C. J. (1991) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)31505-9 · Cited by 84
Marked endogenous activation of the CYP1A1 and CYP1A2 genes in the congenitally jaundiced Gunn rat.
Kapitulnik, J., & Gonzalez, F. J. (1993) · Molecular Pharmacology · doi:10.1016/s0026-895x(25)13648-1 · Cited by 83
Waller, C. L., & McKinney, J. D. (1992) · Journal of Medicinal Chemistry · doi:10.1021/jm00098a010 · Cited by 80
Banner, C. D., Göttlicher, M., Widmark, E., Sjövall, J., Jj, R., & Gustafsson, J. (1993) · Journal of Lipid Research · doi:10.1016/s0022-2275(20)36951-0 · Cited by 76
Allen, S. W., Mueller, L., Williams, S. N., Quattrochi, L. C., & Raucy, J. L. (2001) · PubMed · Cited by 74
Evidence That Murine Preimplantation Embryos Express Aryl Hydrocarbon Receptor
Peters, J. M., & Wiley, L. M. (1995) · Toxicology and Applied Pharmacology · doi:10.1006/taap.1995.1186 · Cited by 70
Species-specific binding of transformed Ah receptor to a dioxin responsive transcriptional enhancer
Bank, P. A., Yao, E. F., Phelps, C. L., Harper, P. A., & Denison, M. S. (1992) · European Journal of Pharmacology Environmental Toxicology and Pharmacology · doi:10.1016/0926-6917(92)90016-6 · Cited by 64
Self-citationProduction ofahreceptor ligands in rat fecal suspensions containing tryptophan or indole‐3‐carbinol
Perdew, G. H., & Babbs, C. F. (1991) · Nutrition and Cancer · doi:10.1080/01635589109514159 · Cited by 63
Mhin, B. J., Lee, J.-E., & Choi, W. (2001) · Journal of the American Chemical Society · doi:10.1021/ja016913q · Cited by 63
A model for recognition of polychlorinated dibenzo‐p‐dioxins by the aryl hydrocarbon receptor
Procopio, M., Lahm, A., Tramontano, A., Bonati, L., & Pitea, D. (2002) · European Journal of Biochemistry · doi:10.1046/j.0014-2956.2002.02619.x · Cited by 61 · cited 2×
“The LBD model has also led to preliminary hypotheses on the residues that may be involved in ligand binding within the cavity [124].”
BackgroundMethodSelf-citationMohammadpour, H. A., Murray, W. J., & STOHS, S. J. (1988) · Archives of Environmental Contamination and Toxicology · doi:10.1007/bf01055833 · Cited by 59
Denison, M. S., & Wilkinson, C. F. (1985) · European Journal of Biochemistry · doi:10.1111/j.1432-1033.1985.tb08767.x · Cited by 58
Self-citationKraemer, S. A., Arthur, K. A., Denison, M. S., Smith, W. L., & DeWitt, D. L. (1996) · Archives of Biochemistry and Biophysics · doi:10.1006/abbi.1996.0259 · Cited by 58
Self-citationTithof, P. K., Schiamberg, E., Peters-Golden, M. L., & Ganey, P. E. (1996) · Environmental Health Perspectives · doi:10.1289/ehp.9610452 · Cited by 57
Mukhtar, H., DelTito, B. J., Matgouranis, P. M., Das, M., Asokan, P., & Bickers, D. R. (1986) · Journal of Investigative Dermatology · doi:10.1111/1523-1747.ep12524446 · Cited by 56
Phenobarbital Induction of Gene Expression in a Primary Culture of Rainbow Trout Hepatocytes
Sadar, M. D., Ash, R., Sundqvist, J., Olsson, P., & Andersson, T. B. (1996) · Journal of Biological Chemistry · doi:10.1074/jbc.271.30.17635 · Cited by 56
Aryl Hydrocarbon Receptor Regulation of Ceramide-induced Apoptosis in Murine Hepatoma 1c1c7 Cells
Reiners, J. J., & Clift, R. E. (1999) · Journal of Biological Chemistry · doi:10.1074/jbc.274.4.2502 · Cited by 54
Kikuchi, H., Kato, H., Mizuno, M., Hossain, A., Ikawa, S., Miyazaki, J., & Watanabe, M. (1996) · Archives of Biochemistry and Biophysics · doi:10.1006/abbi.1996.0451 · Cited by 54
Tuppurainen, K. A., & Ruuskanen, J. (2000) · Chemosphere · doi:10.1016/s0045-6535(99)00525-1 · Cited by 53
McGuire, J., Whitelaw, M. L., Pongratz, I., Gustafsson, J. A., & Poellinger, L. (1994) · Molecular and Cellular Biology · doi:10.1128/mcb.14.4.2438 · Cited by 51
Biological sensors: More than one way to sense oxygen
Pellequer, J., Brudler, R., & Getzoff, E. D. (1999) · Current Biology · doi:10.1016/s0960-9822(99)80257-7 · Cited by 49
Fraschini, E., Bonati, L., & Pitea, D. (1996) · The Journal of Physical Chemistry · doi:10.1021/jp952888x · Cited by 47
Self-citationGeneration of ligand binding sites in T4 lysozyme by deficiency-creating substitutions
Baldwin, E. P., Baase, W. A., Zhang, X. C., Feher, V. A., & Matthews, B. W. (1998) · Journal of Molecular Biology · doi:10.1006/jmbi.1997.1606 · Cited by 47
Self-citationPaine, A. J. (1976) · Biochemical Journal · doi:10.1042/bj1580109 · Cited by 46
Perutz, M. F., Paoli, M., & Lesk, A. M. (1999) · Chemistry & Biology · doi:10.1016/s1074-5521(99)80121-5 · Cited by 44
Reaction Pathways ofin vivoStereoselective Conversion of Ethylbenzene to (-)-Mandelic Acid
Sullivan, H. R., Miller, W. M., & McMahon, R. E. (1976) · Xenobiotica · doi:10.3109/00498257609151611 · Cited by 44
Suppressive effects of flavonoids on dioxin toxicity.
Ashida, H. (2000) · Biofactors · doi:10.1002/biof.5520120132 · Cited by 43
Influence of UVA and UVB irradiation on hepatic and cutaneous P450 isoenzymes
Goerz, G., Barnstorf, W., Winnekendonk, G., Bolsen, K., Fritsch, C., Kalka, K., & Tsambaos, D. (1996) · Archives of Dermatological Research · doi:10.1007/s004030050151 · Cited by 43
2,3,7,8-Tetrachlorodibenzo-p-dioxin (TCDD)-induced decrease in the fluidity of rat liver membranes
Alsharif, N. Z., Grandjean, C. J., Murray, W. J., & STOHS, S. J. (1990) · Xenobiotica · doi:10.3109/00498259009046913 · Cited by 41
Amakura, Y., Tsutsumi, T., Nakamura, M., Kitagawa, H., Fujino, J., Sasaki, K., Yoshida, T., & TOYODA, M. (2002) · Biological and Pharmaceutical Bulletin · doi:10.1248/bpb.25.272 · Cited by 39
Kafafi, S. A., Afeefy, H. Y., Said, H. K., & Kafafi, A. G. (1993) · Chemical Research in Toxicology · doi:10.1021/tx00033a012 · Cited by 37
Influence of chronic UV-light exposure on hepatic and cutaneous monooxygenases
Goerz, G., Merk, H. F., Bolsen, K., Tsambaos, D., & Berger, H. (1983) · Cellular and Molecular Life Sciences · doi:10.1007/bf01963137 · Cited by 37
Constitutive and inducible expression of drug metabolizing enzymes in cultured human keratinocytes
Vecchini, F., Macé, K., Magdalou, J., Mahé, Y. F., Bernard, B. A., & Shroot, B. (1995) · British Journal of Dermatology · doi:10.1111/j.1365-2133.1995.tb08618.x · Cited by 35
Paine, A. J., & Francis, J. E. (1980) · Chemico-Biological Interactions · doi:10.1016/0009-2797(80)90057-5 · Cited by 35
Transient Expression of CYP1A1 in Rat Epithelial Cells Cultured in Suspension
Monk, S. A., Denison, M. S., & Rice, R. H. (2001) · Archives of Biochemistry and Biophysics · doi:10.1006/abbi.2001.2475 · Cited by 33
Self-citationLee, C. A., Lawrence, B. P., Kerkvliet, N. I., & Rifkind, A. B. (1998) · Toxicology and Applied Pharmacology · doi:10.1006/taap.1998.8468 · Cited by 32
Characterization of prostaglandin‐F 2α‐binding sites on rat hepatocyte plasma membranes
Neuschäfer‐Rube, F., Püschel, G. P., & Jungermann, K. A. (1993) · European Journal of Biochemistry · doi:10.1111/j.1432-1033.1993.tb19883.x · Cited by 30
Bonati, L., Fraschini, E., Lasagni, M., Modoni, E. P., & Pitea, D. (1995) · Journal of Molecular Structure THEOCHEM · doi:10.1016/0166-1280(95)04171-2 · Cited by 30
Self-citationPossible Role of Arachidonic Acid in Stress‐Induced Cytochrome P450IA1 Activity1
Mufti, N. A., & Shuler, M. L. (1996) · Biotechnology Progress · doi:10.1021/bp960067j · Cited by 27
The Ah Receptor Signal Transduction Pathw ay
(1998) · CRC Press eBooks · doi:10.1201/9781439805923-8 · Cited by 23
Nguyen, T., Paterson, I. A., Juorio, A. V., Greenshaw, A. J., & Boulton, A. A. (1989) · Brain Research · doi:10.1016/0006-8993(89)91539-4 · Cited by 22
Lawrence, B. (1998) · Toxicological Sciences · doi:10.1006/toxs.1997.2418 · Cited by 22
Al-Bayati, Z. A. F., & STOHS, S. J. (1991) · Archives of Environmental Contamination and Toxicology · doi:10.1007/bf01064403 · Cited by 20
Different Inducibility of Cytochrome P-4501A1 mRNA of Human and Mouse by Omeprazole in Culture Cells
Kikuchi, H., Hossain, A., Sagami, I., Ikawa, S., & Watanabe, M. (1995) · Archives of Biochemistry and Biophysics · doi:10.1006/abbi.1995.1085 · Cited by 20
Bonati, L., Fraschini, E., Lasagni, M., & Pitea, D. (1994) · Journal of Molecular Structure THEOCHEM · doi:10.1016/0166-1280(94)80172-x · Cited by 17
Self-citationThe Ah Receptor Can Bind Ligand in the Absence of Receptor-Associated Heat-Shock Protein 90
Phelan, D., Brackney, W. R., & Denison, M. S. (1998) · Archives of Biochemistry and Biophysics · doi:10.1006/abbi.1997.0614 · Cited by 15
Self-citationInduction of CYP1A1 by GABA Receptor Ligands
Sadar, M. D., Westlind, A., Blomstrand, F., & Andersson, T. B. (1996) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.1996.1785 · Cited by 13
Ocular hypotension induced by topical dopaminergic drugs and phosphodiesterase inhibitors
Hariton, C. (1994) · European Journal of Pharmacology · doi:10.1016/0014-2999(94)90060-4 · Cited by 12
Toxicant-receptor interactions : modulation of signal transduction and gene expression
Denison, M. S., & Helferich, W. G. (1998) · Taylor & Francis eBooks · Cited by 11
Self-citationHefti, M. H., Hendle, J., Enroth, C., Vervoort, J. J. M., & Tucker, P. A. (2001) · Acta Crystallographica Section D Biological Crystallography · doi:10.1107/s0907444901015657 · Cited by 6
Research works printed but not linked: 5
- Bohonowych, 2000, Activation of Ah and estrogen receptor-based cell bioassay systems by extracts of natural dietary herbal supplements, Organohalogen Compd., 45, 240
- Helferich, 1991, Photooxidized products of tryptophan can act as dioxin agonists, Mol. Pharmacol., 40, 674
- Chang, 1998, Constitutive activation of the aromatic hydrocarbon receptor, Mol. Cell. Biol., 18, 525, 10.1128/MCB.18.1.525 · DOI
- Allen, 2001, The use of a high-volume screening procedure to assess the effects of dietary flavonoids on human cyp1a1 expression, Drug Metab. Dispos., 29, 1074
- Nagy, 2002, Development of a green fluorescent protein based cell bioassay for the rapid and inexpensive detection and characterization of AhR agonists, Toxicol. Sci., 65, 200, 10.1093/toxsci/65.2.200 · DOI
Cited by
Sorted by citations
Multitargeted cancer prevention by quercetin
Murakami, A., Ashida, H., & Terao, J. (2008) · Cancer Letters · doi:10.1016/j.canlet.2008.03.046 · Cited by 740
Aryl hydrocarbon receptor control of a disease tolerance defence pathway
Bessede, A., Gargaro, M., Pallotta, M. T., Matino, D., Servillo, G., Brunacci, C., Bicciato, S., Mazza, E. M. C., Macchiarulo, A., Vacca, C., et al. (2014) · Nature · doi:10.1038/nature13323 · Cited by 693
Self-citationIshikawa, M., & Hashimoto, Y. (2011) · Journal of Medicinal Chemistry · doi:10.1021/jm101356p · Cited by 652
NPAS2: A Gas-Responsive Transcription Factor
Dioum, E. M., Rutter, J. P., Tuckerman, J. R., Gonzalez, G., Gilles‐Gonzalez, M., & McKnight, S. L. (2002) · Science · doi:10.1126/science.1078456 · Cited by 432
Effect-directed analysis supporting monitoring of aquatic environments — An in-depth overview
Brack, W., Aı̈t-Aı̈ssa, S., Burgess, R. M., Busch, W., Creusot, N., Paolo, C. D., Escher, B. I., Hewitt, L. M., Hilscherová, K., Hollender, J., et al. (2016) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2015.11.102 · Cited by 414
Metadata
- Authors
- Denison, M. S., Pandini, A., Nagy, S. R., Baldwin, E. P., & Bonati, L.
- Affiliations
- University of California, Davis (US)
- University of Milano-Bicocca (IT)
- Corresponding author
- Denison, Michael S
- Venue
- Chemico-Biological Interactions
- Publisher
- Elsevier BV
- Published
- 2002-09
- Volume
- 141
- Issue
- 1-2
- Pages
- 3-24
- ISSN
- 0009-2797 (ISSN-L)
- OpenAlex
- W1985754063
- Cited by
- 485
- References
- 153
- Citations by year
- 2026: 7 · 2025: 8 · 2024: 12 · 2023: 16 · 2022: 18 · 2021: 7 · 2020: 18 · 2019: 13 · 2018: 18 · 2017: 18 · 2016: 20 · 2015: 16 · 2014: 30 · 2013: 24 · 2012: 30
- FWCI
- 15.36
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Chemico-Biological Interactions (publishedVersion)
- PubMed (publishedVersion)
- BOA (University of Milano-Bicocca) (submittedVersion)
- eScholarship (California Digital Library) (submittedVersion)
- Funders
- National Institutes of Health (5r01es007072-04)
- National Institute of Environmental Health Sciences (ES07059, ES 07685, R01ES007685, ES-07072, ES5707, T32ES007059)
- Topics
- Physical Sciences › Environmental Science › Health, Toxicology and Mutagenesis › Toxic Organic Pollutants Impact
- Life Sciences › Pharmacology, Toxicology and Pharmaceutics › Pharmacology › Pharmacogenetics and Drug Metabolism
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › Carcinogens and Genotoxicity Assessment
- Keywords
- aryl hydrocarbon receptor, ligand binding, receptor activation, ligand-binding domain, aromatic hydrocarbons, crystal structure, signal transduction, transcription factors
- MeSH terms
- Animals, Binding Sites, Humans, Ligands, Protein Binding, Protein Conformation, Signal Transduction, Receptors, Aryl Hydrocarbon
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