The use of metabolising systems for in vitro testing of endocrine disruptors.

Legislation and prospective legislative proposals in for instance the USA, Europe, and Japan require, or may require that chemicals are tested for their ability to disrupt the hormonal systems of mammals. Chemicals found to test positive are considered to be endocrine active substances (EAS) and may be putative endocrine disruptors (EDs). To date, there is still little or no experience with incorporating metabolic and toxicokinetic aspects into in vitro tests for EAS. This is a situation in sharp contrast to genotoxicity testing, where in vitro tests are routinely conducted with and without metabolic capacity. Originally prepared for the Organisation of Economic Cooperation and Development (OECD), this detailed review paper reviews why in vitro assays for EAS should incorporate mammalian systems of metabolism and metabolic enzyme systems, and indicates how this could be done. The background to ED testing, the available test methods, and the role of mammalian metabolism in the activation and the inactivation of both endogenous and exogenous steroids are described. The available types of systems are compared, and the potential problems in incorporating systems in in vitro tests for EAS, and how these might be overcome, are discussed. Lastly, some recommendations for future activities are made.

[1]  J. Gustafsson,et al.  Estrogen Receptor (ER) β Modulates ERα-Mediated Transcriptional Activation by Altering the Recruitment of c-Fos and c-Jun to Estrogen-Responsive Promoters , 2006 .

[2]  Andrew Worth,et al.  Metabolism: A Bottleneck in In Vitro Toxicological Test Development , 2006, Alternatives to laboratory animals : ATLA.

[3]  S. Hood,et al.  Lignans, bacteriocides and organochlorine compounds activate the human pregnane X receptor (PXR). , 2005, Toxicology and applied pharmacology.

[4]  R. Harris,et al.  Non-genomic effects of endocrine disrupters: Inhibition of estrogen sulfotransferase by phenols and chlorinated phenols , 2005, Molecular and Cellular Endocrinology.

[5]  R. Waring,et al.  Endocrine disrupters: A human risk? , 2005, Molecular and Cellular Endocrinology.

[6]  D. B. Ramsden,et al.  The effect of plasticisers on “sulphate supply” enzymes , 2005, Molecular and Cellular Endocrinology.

[7]  Wolfgang Völkel,et al.  QUANTITATION OF BISPHENOL A AND BISPHENOL A GLUCURONIDE IN BIOLOGICAL SAMPLES BY HIGH PERFORMANCE LIQUID CHROMATOGRAPHY-TANDEM MASS SPECTROMETRY , 2005, Drug Metabolism and Disposition.

[8]  N. Vermeulen,et al.  Bioactivation of dibrominated biphenyls by cytochrome P450 activity to metabolites with estrogenic activity and estrogen sulfotransferase inhibition capacity. , 2005, Chemical research in toxicology.

[9]  Oliver Hankinson,et al.  CYP2S1: a short review. , 2005, Toxicology and applied pharmacology.

[10]  H. Yoshioka,et al.  Changes in the mutagenic and estrogenic activities of bisphenol A upon treatment with nitrite. , 2005, Mutation research.

[11]  B. O'dowd,et al.  A G protein-coupled receptor for estrogen: the end of the search? , 2005, Molecular interventions.

[12]  K. Setchell,et al.  S-equol, a potent ligand for estrogen receptor beta, is the exclusive enantiomeric form of the soy isoflavone metabolite produced by human intestinal bacterial flora. , 2005, The American journal of clinical nutrition.

[13]  Ellen Fritsche,et al.  Polychlorinated Biphenyls Disturb Differentiation of Normal Human Neural Progenitor Cells: Clue for Involvement of Thyroid Hormone Receptors , 2005, Environmental health perspectives.

[14]  A. Kong,et al.  Induction of phase I, II and III drug metabolism/transport by xenobiotics , 2005, Archives of pharmacal research.

[15]  C. Carlberg,et al.  Identification of pregnane X receptor binding sites in the regulatory regions of genes involved in bile acid homeostasis. , 2005, Journal of molecular biology.

[16]  J. Milner,et al.  Targets for indole-3-carbinol in cancer prevention. , 2005, Journal of Nutritional Biochemistry.

[17]  T. Thomas,et al.  Differential effects of 16α-hydroxyestrone and 2-methoxyestradiol on cyclin D1 involving the transcription factor ATF-2 in MCF-7 breast cancer cells , 2005 .

[18]  F Peter Guengerich,et al.  Principles of covalent binding of reactive metabolites and examples of activation of bis-electrophiles by conjugation. , 2005, Archives of biochemistry and biophysics.

[19]  G. Schmuck,et al.  Screening for estrogenicity and anti-estrogenicity: a critical evaluation of an MVLN cell-based transactivation assay. , 2005, Toxicology letters.

[20]  H. Lichtenberg-Fraté,et al.  In vitro bioactivity of 17α-estradiol , 2004, The Journal of Steroid Biochemistry and Molecular Biology.

[21]  M. Jacobs,et al.  In silico tools to aid risk assessment of endocrine disrupting chemicals. , 2004, Toxicology.

[22]  A. Ghazali,et al.  Effects of culture with TNF-α, TGF-β and insulin on sulphotransferase (SULT 1A1 and 1A3) activity in human colon and neuronal cell lines , 2004 .

[23]  Anders Karlén,et al.  Structural analysis of CYP2C9 and CYP2C5 and an evaluation of commonly used molecular modeling techniques. , 2004, Drug metabolism and disposition: the biological fate of chemicals.

[24]  M. Hawkins,et al.  The unusual binding properties of the third distinct teleost estrogen receptor subtype ERbetaa are accompanied by highly conserved amino acid changes in the ligand binding domain. , 2004, Endocrinology.

[25]  T. Uchida,et al.  Cytochrome P450 gene expression levels in peripheral blood mononuclear cells in comparison with the liver , 2004, Cancer science.

[26]  J. Freudenheim,et al.  Breast cancer risk in premenopausal women is inversely associated with consumption of broccoli, a source of isothiocyanates, but is not modified by GST genotype. , 2004, The Journal of nutrition.

[27]  Ovanes Mekenyan,et al.  Identification of the structural requirements for mutagenicity by incorporating molecular flexibility and metabolic activation of chemicals I: TA100 model. , 2004, Chemical research in toxicology.

[28]  Y. Kuroda,et al.  Polychlorinated Biphenyls Suppress Thyroid Hormone Receptor-mediated Transcription through a Novel Mechanism* , 2004, Journal of Biological Chemistry.

[29]  Sabcho D Dimitrov,et al.  A systematic approach to simulating metabolism in computational toxicology. I. The TIMES heuristic modelling framework. , 2004, Current pharmaceutical design.

[30]  S. Hoffman,et al.  Epidermal CYP2 family cytochromes P450. , 2004, Toxicology and applied pharmacology.

[31]  S. Ohta,et al.  Potent estrogenic metabolites of bisphenol A and bisphenol B formed by rat liver S9 fraction: their structures and estrogenic potency. , 2004, Toxicological sciences : an official journal of the Society of Toxicology.

[32]  K. Lai,et al.  Modulation of AhR-mediated CYP1A1 mRNA and EROD activities by 17beta-estradiol and dexamethasone in TCDD-induced H411E cells. , 2004, Toxicological sciences : an official journal of the Society of Toxicology.

[33]  C. Handschin,et al.  Induction of Drug Metabolism: The Role of Nuclear Receptors , 2003, Pharmacological Reviews.

[34]  Xinxin Ding,et al.  Human extrahepatic cytochromes P450: function in xenobiotic metabolism and tissue-selective chemical toxicity in the respiratory and gastrointestinal tracts. , 2003, Annual review of pharmacology and toxicology.

[35]  W. Dhooge,et al.  Endocrine disruptors: effects on male fertility and screening tools for their assessment. , 2003, Toxicology in vitro : an international journal published in association with BIBRA.

[36]  N. Vermeulen,et al.  675 Formation of estrogenic metabolites from polycyclic aromatic hydrocarbons and halogenated biphenyls by cytochrome P450 activity and development of a predictive computational model for binding to the estrogen receptor , 2003 .

[37]  J. Gustafsson,et al.  Estrogen signaling: a subtle balance between ER alpha and ER beta. , 2003, Molecular interventions.

[38]  David E. Williams,et al.  Evaluation of chronic dietary exposure to indole-3-carbinol and absorption-enhanced 3,3'-diindolylmethane in sprague-dawley rats. , 2003, Toxicological sciences : an official journal of the Society of Toxicology.

[39]  Jos H Beijnen,et al.  An update on in vitro test methods in human hepatic drug biotransformation research: pros and cons. , 2003, Toxicology and applied pharmacology.

[40]  L. Pedersen,et al.  Crystallographic analysis of a hydroxylated polychlorinated biphenyl (OH-PCB) bound to the catalytic estrogen binding site of human estrogen sulfotransferase. , 2003, Environmental health perspectives.

[41]  C. Tohyama,et al.  Modulation of oestrogen receptor signalling by association with the activated dioxin receptor , 2003, Nature.

[42]  Robert Combes,et al.  A Critical Assessment of the European Commission's Proposals for the Risk Assessment and Registration of Chemical Substances in the European Union , 2003, Alternatives to laboratory animals : ATLA.

[43]  Michael Balls,et al.  How Much Flexibility is Possible When Validating New In Vivo and In Vitro Toxicity Test Methods? , 2003, Alternatives to laboratory animals : ATLA.

[44]  Tetsuo Satoh,et al.  Tissue distribution of mRNA expression of human cytochrome P450 isoforms assessed by high-sensitivity real-time reverse transcription PCR. , 2003, Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan.

[45]  G. Ferron,et al.  Quantitation of cytochrome P450 mRNA levels in human skin. , 2003, Analytical biochemistry.

[46]  Robert M. Harris,et al.  Environmental endocrine disrupters dysregulate estrogen metabolism and Ca2+ homeostasis in fish and mammals via receptor-independent mechanisms. , 2003, Comparative biochemistry and physiology. Part A, Molecular & integrative physiology.

[47]  佐藤 哲男,et al.  資料 Tissue Distribution of mRNA Expression of Human Cytochrome P450 Isoforms Assessed by High-Sensitivity Real-Time Reverse Transcription PCR , 2003 .

[48]  S. Kitamura,et al.  Estrogenic activity of an environmental pollutant, 2-nitrofluorene, after metabolic activation by rat liver microsomes. , 2003, Biochemical and biophysical research communications.

[49]  Clay W Scott,et al.  A homogeneous in vitro functional assay for estrogen receptors: coactivator recruitment. , 2003, Molecular endocrinology.

[50]  R. Evans,et al.  A nuclear receptor-mediated xenobiotic response and its implication in drug metabolism and host protection. , 2003, Current drug metabolism.

[51]  X. Shu,et al.  Urinary estrogen metabolites and breast cancer: differential pattern of risk found with pre- versus post-treatment collection , 2003, Steroids.

[52]  O. Fardel,et al.  Pregnane X receptor-dependent and -independent effects of 2-acetylaminofluorene on cytochrome P450 3A23 expression and liver cell proliferation. , 2003, Biochemical and biophysical research communications.

[53]  H. Glatt,et al.  Heterologous Expression of Mouse Cytochrome P450 2e1 in V79 Cells: Construction and Characterisation of the Cell Line and Comparison with V79 Cell Lines Stably Expressing Rat P450 2E1 and Human P450 2E1 , 2003, Alternatives to laboratory animals : ATLA.

[54]  M. Jacobs,et al.  Silent Invaders: Pesticides, Livelihoods, and Women's Health , 2002 .

[55]  N. Coldham,et al.  A binary screening assay for pro-oestrogens in food: metabolic activation using hepatic microsomes and detection with oestrogen sensitive recombinant yeast cells , 2002, Food additives and contaminants.

[56]  D. Kupfer,et al.  Enantioselective metabolism of the endocrine disruptor pesticide methoxychlor by human cytochromes P450 (P450s): major differences in selective enantiomer formation by various P450 isoforms. , 2002, Drug metabolism and disposition: the biological fate of chemicals.

[57]  S. Kitamura,et al.  Estrogenic activity of styrene oligomers after metabolic activation by rat liver microsomes. , 2002, Environmental health perspectives.

[58]  Richard E Peterson,et al.  A ligand for the aryl hydrocarbon receptor isolated from lung , 2002, Proceedings of the National Academy of Sciences of the United States of America.

[59]  M. van den Berg,et al.  In vitro antiestrogenic effects of aryl methyl sulfone metabolites of polychlorinated biphenyls and 2,2-bis(4-chlorophenyl)-1,1-dichloroethene on 17beta-estradiol-induced gene expression in several bioassay systems. , 2002, Toxicological sciences : an official journal of the Society of Toxicology.

[60]  Wolfgang Völkel,et al.  Metabolism and kinetics of bisphenol a in humans at low doses following oral administration. , 2002, Chemical research in toxicology.

[61]  A. D. Vethaak,et al.  Comparison of in vivo and in vitro reporter gene assays for short-term screening of estrogenic activity. , 2002, Environmental science & technology.

[62]  M. E. Hahn,et al.  Aryl hydrocarbon receptors: diversity and evolution. , 2002, Chemico-biological interactions.

[63]  D. Kupfer,et al.  Metabolism of the endocrine disruptor pesticide-methoxychlor by human P450s: pathways involving a novel catechol metabolite. , 2002, Drug metabolism and disposition: the biological fate of chemicals.

[64]  J. Lemmen,et al.  Detection of oestrogenic activity of steroids present during mammalian gestation using oestrogen receptor alpha- and oestrogen receptor beta-specific in vitro assays. , 2002, Journal of Endocrinology.

[65]  K. Setchell,et al.  Evidence for lack of absorption of soy isoflavone glycosides in humans, supporting the crucial role of intestinal metabolism for bioavailability. , 2002, The American journal of clinical nutrition.

[66]  K. Crofton,et al.  Comparative responsiveness of hypothyroxinemia and hepatic enzyme induction in Long-Evans rats versus C57BL/6J mice exposed to TCDD-like and phenobarbital-like polychlorinated biphenyl congeners. , 2002, Toxicological sciences : an official journal of the Society of Toxicology.

[67]  B. Goodwin,et al.  Transcriptional regulation of the human CYP3A4 gene by the constitutive androstane receptor. , 2002, Molecular pharmacology.

[68]  Juliette Legler,et al.  Detection of estrogenic activity in sediment-associated compounds using in vitro reporter gene assays. , 2002, The Science of the total environment.

[69]  K. Scotto,et al.  Ecteinascidin-743 inhibits activated but not constitutive transcription. , 2002, Cancer research.

[70]  M. Denison,et al.  Analysis of the antiestrogenic activity of 2,3,7,8-tetrachlorodibenzo-p-dioxin in human ovarian carcinoma BG-1 cells. , 2002, Molecular pharmacology.

[71]  K. Howdeshell A model of the development of the brain as a construct of the thyroid system. , 2002, Environmental health perspectives.

[72]  R. Teshima,et al.  mRNA Expression of Multiple Cytochrome P450 Isozymes in Four Types of Cultured Skin Cells , 2002, International Archives of Allergy and Immunology.

[73]  T. Matsuda,et al.  Activation of the aryl hydrocarbon receptor by methyl yellow and related congeners: structure-activity relationships in halogenated derivatives. , 2002, Biological & pharmaceutical bulletin.

[74]  Johansson Mk,et al.  Effects of 3-MeSO2-DDE and some CYP inhibitors on glucocorticoid steroidogenesis in the H295R human adrenocortical carcinoma cell line. , 2002 .

[75]  R. S. Lord,et al.  Estrogen metabolism and the diet-cancer connection: rationale for assessing the ratio of urinary hydroxylated estrogen metabolites. , 2002, Alternative medicine review : a journal of clinical therapeutic.

[76]  T. Goehl,et al.  Environmental Health Perspectives , 2002, Environmental Health Perspectives.

[77]  A. Kortenkamp,et al.  Something from "nothing"--eight weak estrogenic chemicals combined at concentrations below NOECs produce significant mixture effects. , 2002, Environmental science & technology.

[78]  A. Hatagima Genetic polymorphisms and metabolism of endocrine disruptors in cancer susceptibility. , 2002, Cadernos de saude publica.

[79]  H. Glatt,et al.  Potent inhibition of estrogen sulfotransferase by hydroxylated metabolites of polyhalogenated aromatic hydrocarbons reveals alternative mechanism for estrogenic activity of endocrine disrupters. , 2002, The Journal of clinical endocrinology and metabolism.

[80]  M. Denison,et al.  Development of a green fluorescent protein-based cell bioassay for the rapid and inexpensive detection and characterization of ah receptor agonists. , 2002, Toxicological sciences : an official journal of the Society of Toxicology.

[81]  D. G. McCarver,et al.  The ontogeny of human drug-metabolizing enzymes: phase II conjugation enzymes and regulatory mechanisms. , 2002, The Journal of pharmacology and experimental therapeutics.

[82]  D. G. McCarver,et al.  The ontogeny of human drug-metabolizing enzymes: phase I oxidative enzymes. , 2002, The Journal of pharmacology and experimental therapeutics.

[83]  D. Lewis,et al.  Steroid hormone receptors and dietary ligands: a selected review , 2002, Proceedings of the Nutrition Society.

[84]  S Dimitrov,et al.  Probabilistic assessment of biodegradability based on metabolic pathways: CATABOL System , 2002, SAR and QSAR in environmental research.

[85]  T. Carter,et al.  Indole-3-carbinol and diindolylmethane induce apoptosis of human cervical cancer cells and in murine HPV16-transgenic preneoplastic cervical epithelium. , 2001, The Journal of nutrition.

[86]  M. Gallo,et al.  Regulation of cell cycle and cyclins by 16alpha-hydroxyestrone in MCF-7 breast cancer cells. , 2001, Journal of molecular endocrinology.

[87]  C Sonnenschein,et al.  The two faces of janus: sex steroids as mediators of both cell proliferation and cell death. , 2001, Journal of the National Cancer Institute.

[88]  S. Belcher,et al.  Estrogenic actions in the brain: estrogen, phytoestrogens, and rapid intracellular signaling mechanisms. , 2001, The Journal of pharmacology and experimental therapeutics.

[89]  S. Bull,et al.  A Genetically Engineered Cell-based System for Detecting Metabolism-mediated Toxicity , 2001, Alternatives to laboratory animals : ATLA.

[90]  S. Safe,et al.  Differential gene expression in response to methoxychlor and estradiol through ERalpha, ERbeta, and AR in reproductive tissues of female mice. , 2001, Toxicological sciences : an official journal of the Society of Toxicology.

[91]  S. Ohta,et al.  Metabolic activation of bisphenol A by rat liver S9 fraction. , 2001, Toxicological sciences : an official journal of the Society of Toxicology.

[92]  Y. Hashimoto,et al.  Measurement of estrogenic activity of chemicals for the development of new dental polymers. , 2001, Toxicology in vitro : an international journal published in association with BIBRA.

[93]  A Worth,et al.  The use of genetically engineered cells for assessing CYP2D6-related polymorphic effects. , 2001, Toxicology in vitro : an international journal published in association with BIBRA.

[94]  H. Yamazaki,et al.  Inhibition and inactivation of human cytochrome P450 isoforms by phenethyl isothiocyanate. , 2001, Drug metabolism and disposition: the biological fate of chemicals.

[95]  V A Baker,et al.  Endocrine disrupters--testing strategies to assess human hazard. , 2001, Toxicology in vitro : an international journal published in association with BIBRA.

[96]  J B Houston,et al.  Optimizing drug development: strategies to assess drug metabolism/transporter interaction potential--towards a consensus. , 2001, British journal of clinical pharmacology.

[97]  P. Yen,et al.  Physiological and molecular basis of thyroid hormone action. , 2001, Physiological reviews.

[98]  E L LeCluyse,et al.  Human hepatocyte culture systems for the in vitro evaluation of cytochrome P450 expression and regulation. , 2001, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

[99]  J. McLachlan,et al.  Environmental signaling: what embryos and evolution teach us about endocrine disrupting chemicals. , 2001, Endocrine reviews.

[100]  A. D. Rodrigues,et al.  Role of human liver cytochrome P4503A in the metabolism of etoricoxib, a novel cyclooxygenase-2 selective inhibitor. , 2001, Drug metabolism and disposition: the biological fate of chemicals.

[101]  S. Dehal,et al.  Mechanism of induction of cytochrome p450 enzymes by the proestrogenic endocrine disruptor pesticide-methoxychlor: interactions of methoxychlor metabolites with the constitutive androstane receptor system. , 2001, Drug metabolism and disposition: the biological fate of chemicals.

[102]  R. J. Riley,et al.  Development of a Generalized, Quantitative Physicochemical Model of CYP3A4 Inhibition for Use in Early Drug Discovery , 2001, Pharmaceutical Research.

[103]  S. Safe,et al.  2,3,7,8-Tetrachlorodibenzo-p-dioxin and diindolylmethanes differentially induce cytochrome P450 1A1, 1B1, and 19 in H295R human adrenocortical carcinoma cells. , 2001, Toxicological sciences : an official journal of the Society of Toxicology.

[104]  B. M. Forman,et al.  The orphan nuclear receptor SXR coordinately regulates drug metabolism and efflux , 2001, Nature Medicine.

[105]  Z. Luo,et al.  Molecular regulation of genes encoding xenobiotic-metabolizing enzymes: mechanisms involving endogenous factors. , 2001, Drug metabolism and disposition: the biological fate of chemicals.

[106]  A. Cupp,et al.  Actions of the endocrine disruptor methoxychlor and its estrogenic metabolite on in vitro embryonic rat seminiferous cord formation and perinatal testis growth. , 2001, Reproductive toxicology.

[107]  K M Crofton,et al.  Effects of short-term in vivo exposure to polybrominated diphenyl ethers on thyroid hormones and hepatic enzyme activities in weanling rats. , 2001, Toxicological sciences : an official journal of the Society of Toxicology.

[108]  C. Masimirembwa,et al.  Competitive CYP2C9 inhibitors: enzyme inhibition studies, protein homology modeling, and three-dimensional quantitative structure-activity relationship analysis. , 2001, Molecular pharmacology.

[109]  J. Ashby,et al.  Comparison of the modulatory effects of human and rat liver microsomal metabolism on the estrogenicity of bisphenol A: implications for extrapolation to humans. , 2001, The Journal of pharmacology and experimental therapeutics.

[110]  I. Meerts,et al.  In vitro estrogenicity of polybrominated diphenyl ethers, hydroxylated PDBEs, and polybrominated bisphenol A compounds. , 2001, Environmental health perspectives.

[111]  S. Frankenberg,et al.  Expression of multiple cytochrome p450 enzymes and multidrug resistance-associated transport proteins in human skin keratinocytes. , 2001, The Journal of investigative dermatology.

[112]  D. Boerboom,et al.  Molecular Characterization of Bovine Prostaglandin G/H Synthase-2 and Regulation in Uterine Stromal Cells1 , 2001, Biology of reproduction.

[113]  J. Ashby,et al.  Assessment of the effects of metabolism on the estrogenic activity of xenoestrogens: a two-stage approach coupling human liver microsomes and a yeast estrogenicity assay. , 2001, The Journal of pharmacology and experimental therapeutics.

[114]  J. Thomsen,et al.  Mechanisms of estrogen action. , 2001, Physiological reviews.

[115]  H. Glatt,et al.  Sulfotransferases in the bioactivation of xenobiotics. , 2000, Chemico-biological interactions.

[116]  E. Rosen,et al.  Indole-3-Carbinol Is a Negative Regulator of Estrogen Receptor-α Signaling in Human Tumor Cells , 2000 .

[117]  Carolyn L. Smith,et al.  Molecular mechanisms of selective estrogen receptor modulator (SERM) action. , 2000, The Journal of pharmacology and experimental therapeutics.

[118]  G. Williamson,et al.  7-Methylsulfinylheptyl and 8-methylsulfinyloctyl isothiocyanates from watercress are potent inducers of phase II enzymes. , 2000, Carcinogenesis.

[119]  D. Moore,et al.  The nuclear receptor CAR mediates specific xenobiotic induction of drug metabolism , 2000, Nature.

[120]  Donald P. McDonnell,et al.  Interaction of Methoxychlor and Related Compounds with Estrogen Receptor α and β, and Androgen Receptor: Structure-Activity Studies , 2000 .

[121]  J. Thornton,et al.  Identification of a third distinct estrogen receptor and reclassification of estrogen receptors in teleosts. , 2000, Proceedings of the National Academy of Sciences of the United States of America.

[122]  C L Crespi,et al.  Fluorometric High‐Throughput Screening for Inhibitors of Cytochrome P450 , 2000, Annals of the New York Academy of Sciences.

[123]  H Fang,et al.  Quantitative comparisons of in vitro assays for estrogenic activities. , 2000, Environmental health perspectives.

[124]  R D Combes,et al.  The use of structure-activity relationships and markers of cell toxicity to detect non-genotoxic carcinogens. , 2000, Toxicology in vitro : an international journal published in association with BIBRA.

[125]  J. Fuchs,et al.  Effect of methoxychlor administration to male rats on hepatic, microsomal iodothyronine 5'-deiodinase, form I. , 2000, The Journal of pharmacology and experimental therapeutics.

[126]  L. Moore,et al.  St. John's wort induces hepatic drug metabolism through activation of the pregnane X receptor. , 2000, Proceedings of the National Academy of Sciences of the United States of America.

[127]  J. Potter,et al.  Brassica vegetables increase and apiaceous vegetables decrease cytochrome P450 1A2 activity in humans: changes in caffeine metabolite ratios in response to controlled vegetable diets. , 2000, Carcinogenesis.

[128]  S. Safe Endocrine disruptors and human health--is there a problem? An update. , 2000, Environmental health perspectives.

[129]  Terada,et al.  Cytochrome P450 2E1: its clinical and toxicological role , 2000, Journal of clinical pharmacy and therapeutics.

[130]  L. Moore,et al.  Orphan Nuclear Receptors Constitutive Androstane Receptor and Pregnane X Receptor Share Xenobiotic and Steroid Ligands* , 2000, The Journal of Biological Chemistry.

[131]  S. Seidel,et al.  Ah receptor-based chemical screening bioassays: application and limitations for the detection of Ah receptor agonists. , 2000, Toxicological sciences : an official journal of the Society of Toxicology.

[132]  J. Ashby Validation of In Vitro and In Vivo Methods for Assessing Endocrine Disrupting Chemicals , 2000, Toxicologic pathology.

[133]  D. Moore,et al.  The Xenobiotic Compound 1,4-Bis[2-(3,5-Dichloropyridyloxy)]Benzene Is an Agonist Ligand for the Nuclear Receptor CAR , 2000, Molecular and Cellular Biology.

[134]  H. Glatt,et al.  Potent inhibition of estrogen sulfotransferase by hydroxylated PCB metabolites: a novel pathway explaining the estrogenic activity of PCBs. , 2000, Endocrinology.

[135]  N Ing,et al.  A rapid and sensitive reporter gene that uses green fluorescent protein expression to detect chemicals with estrogenic activity. , 2000, Toxicological sciences : an official journal of the Society of Toxicology.

[136]  B. Bhaskar Gollapudi,et al.  Incorporation of S-9 activation into an ER-α transactivation assay☆ , 2000 .

[137]  M. Cronin,et al.  Computational methods for the prediction of drug toxicity. , 2000, Current opinion in drug discovery & development.

[138]  Y. Masuda,et al.  Reduction of serum thyroxine concentrations by methylsulfonyl metabolites of tetra-, penta- and hexachlorinated biphenyls in male Sprague-Dawley rats. , 2000, Chemosphere.

[139]  M. Negishi,et al.  Regulation of cytochrome P450 (CYP) genes by nuclear receptors. , 2000, The Biochemical journal.

[140]  L. Poellinger Mechanistic aspects the dioxin (aryl hydrocarbon) receptor , 2000, Food additives and contaminants.

[141]  Hong Wang,et al.  Activation of the human estrogen receptor by the antiestrogens ICI 182,780 and tamoxifen in yeast genetic systems: implications for their mechanism of action. , 2000, Proceedings of the National Academy of Sciences of the United States of America.

[142]  B. Burchell,et al.  Drug-mediated toxicity caused by genetic deficiency of UDP-glucuronosyltransferases. , 2000, Toxicology letters.

[143]  M. Denison,et al.  Development and modification of a recombinant cell bioassay to directly detect halogenated and polycyclic aromatic hydrocarbons in serum. , 2000, Toxicological sciences : an official journal of the Society of Toxicology.

[144]  M. Kunitomi,et al.  Endocrine disrupting chemicals, phthalic acid and nonylphenol, activate Pregnane X receptor-mediated transcription. , 2000, Molecular endocrinology.

[145]  U. Gundert-Remy,et al.  CYP2E1 expression in bone marrow and its intra- and interspecies variability: approaches for a more reliable extrapolation from one species to another in the risk assessment of chemicals , 2000, Archives of Toxicology.

[146]  F. Oesch,et al.  CRYOPRESERVED PRIMARY HEPATOCYTES AS A CONSTANTLY AVAILABLE IN VITRO MODEL FOR THE EVALUATION OF HUMAN AND ANIMAL DRUG METABOLISM AND ENZYME INDUCTION* , 2000, Drug metabolism reviews.

[147]  R D Combes,et al.  Endocrine Disruptors: A Critical Review of In Vitro and In Vivo Testing Strategies for Assessing Their Toxic Hazard to Humans , 2000, Alternatives to laboratory animals : ATLA.

[148]  Y Ohno,et al.  Metabolic activation of o-phenylphenol to a major cytotoxic metabolite, phenylhydroquinone: role of human CYP1A2 and rat CYP2C11/CYP2E1 , 2000, Xenobiotica; the fate of foreign compounds in biological systems.

[149]  C. Wolf,et al.  Merits and limitations of recombinant models for the study of human P450-mediated drug metabolism and toxicity: an intralaboratory comparison. , 1999, Drug metabolism reviews.

[150]  H. Glatt,et al.  Molecular studies on the toxifying effects by genetically engineered cytochromes P450. , 1999, Drug metabolism reviews.

[151]  I. Purchase,et al.  Ethical review of regulatory toxicology guidelines involving experiments on animals: the example of endocrine disrupters. , 1999, Toxicological sciences : an official journal of the Society of Toxicology.

[152]  G. Kearns,et al.  Cytochrome P450 3A , 1999, Clinical pharmacokinetics.

[153]  S. Safe,et al.  Differential Interaction of the Methoxychlor Metabolite 2,2-Bis-(p-Hydroxyphenyl)-1,1,1-Trichloroethane with Estrogen Receptors α and β1. , 1999, Endocrinology.

[154]  D. Lewis,et al.  Molecular modelling of CYP1 family enzymes CYP1A1, CYP1A2, CYP1A6 and CYP1B1 based on sequence homology with CYP102. , 1999, Toxicology.

[155]  D. Belsham,et al.  Estrogen Directly Represses Gonadotropin-Releasing Hormone (GnRH) Gene Expression in Estrogen Receptor-α (ERα)- and ERβ-Expressing GT1-7 GnRH Neurons1. , 1999, Endocrinology.

[156]  P. Mak,et al.  A yeast screen system for aromatase inhibitors and ligands for androgen receptor: yeast cells transformed with aromatase and androgen receptor. , 1999, Environmental health perspectives.

[157]  P. Souček Expression of cytochrome P450 2A6 in Escherichia coli: purification, spectral and catalytic characterization, and preparation of polyclonal antibodies. , 1999, Archives of biochemistry and biophysics.

[158]  C. Masimirembwa,et al.  Heterologous expression and kinetic characterization of human cytochromes P-450: validation of a pharmaceutical tool for drug metabolism research. , 1999, Drug metabolism and disposition: the biological fate of chemicals.

[159]  D. Waxman,et al.  P450 gene induction by structurally diverse xenochemicals: central role of nuclear receptors CAR, PXR, and PPAR. , 1999, Archives of biochemistry and biophysics.

[160]  T. Inaba,et al.  Relationship between mRNA levels quantified by reverse transcription-competitive PCR and metabolic activity of CYP3A4 and CYP2E1 in human liver. , 1999, Biochemical and biophysical research communications.

[161]  R. Panettieri,et al.  Up-regulation of ICAM-1 by cytokines in human tracheal smooth muscle cells involves an NF-kappa B-dependent signaling pathway that is only partially sensitive to dexamethasone. , 1999, Journal of immunology.

[162]  R. Gebhardt,et al.  Improved Determination of Drug Metabolism by Perifusion of Recombinant V79 Cells Carrying Human CYP3A4. , 1999, Toxicology in vitro : an international journal published in association with BIBRA.

[163]  S. Safe,et al.  Interactions of nuclear receptor coactivator/corepressor proteins with the aryl hydrocarbon receptor complex. , 1999, Archives of biochemistry and biophysics.

[164]  S Coecke,et al.  The use of Long-term Hepatocyte Cultures for Detecting Induction of Drug Metabolising Enzymes: The Current Status , 1999, Alternatives to laboratory animals : ATLA.

[165]  F. Gonzalez,et al.  Specific dehydrogenation of 3-methylindole and epoxidation of naphthalene by recombinant human CYP2F1 expressed in lymphoblastoid cells. , 1999, Drug metabolism and disposition: the biological fate of chemicals.

[166]  U. Gundert-Remy,et al.  CYP2E1-dependent benzene toxicity: the role of extrahepatic benzene metabolism , 1999, Archives of Toxicology.

[167]  B. McEwen,et al.  Estrogen actions in the central nervous system. , 1999, Endocrine reviews.

[168]  A. Li,et al.  Cryopreserved human hepatocytes: characterization of drug-metabolizing enzyme activities and applications in higher throughput screening assays for hepatotoxicity, metabolic stability, and drug-drug interaction potential. , 1999, Chemico-biological interactions.

[169]  S. Dehal,et al.  Cytochrome P-450 3A and 2D6 catalyze ortho hydroxylation of 4-hydroxytamoxifen and 3-hydroxytamoxifen (droloxifene) yielding tamoxifen catechol: involvement of catechols in covalent binding to hepatic proteins. , 1999, Drug metabolism and disposition: the biological fate of chemicals.

[170]  D. Eaton,et al.  Concise review of the glutathione S-transferases and their significance to toxicology. , 1999, Toxicological sciences : an official journal of the Society of Toxicology.

[171]  M. Morrow,et al.  Tamoxifen, raloxifene, and the prevention of breast cancer. , 1999, Endocrine reviews.

[172]  J. Linget,et al.  Automation of metabolic stability studies in microsomes, cytosol and plasma using a 215 Gilson liquid handler. , 1999, Journal of pharmaceutical and biomedical analysis.

[173]  K. Crofton,et al.  Screening methods for thyroid hormone disruptors. , 1999, Environmental health perspectives.

[174]  J. Gierthy,et al.  Rapid assay for oestrogen receptor binding to PCB metabolites. , 1999, Toxicology in vitro : an international journal published in association with BIBRA.

[175]  J. McLachlan,et al.  Potential mechanisms of thyroid disruption in humans: interaction of organochlorine compounds with thyroid receptor, transthyretin, and thyroid-binding globulin. , 1999, Environmental health perspectives.

[176]  H. Vaudry,et al.  Neurosteroids: expression of steroidogenic enzymes and regulation of steroid biosynthesis in the central nervous system. , 1999, Pharmacological reviews.

[177]  S. Hecht,et al.  Chemoprevention of cancer by isothiocyanates, modifiers of carcinogen metabolism. , 1999, The Journal of nutrition.

[178]  A D Vethaak,et al.  Development of a stably transfected estrogen receptor-mediated luciferase reporter gene assay in the human T47D breast cancer cell line. , 1999, Toxicological sciences : an official journal of the Society of Toxicology.

[179]  H. Leffers,et al.  Comparison of short-term estrogenicity tests for identification of hormone-disrupting chemicals. , 1999 .

[180]  S. Nilsson,et al.  Interactions between methylsulfonyl PCBs and the glucocorticoid receptor. , 1998, Environmental health perspectives.

[181]  S. Clarke In vitro assessment of human cytochrome P450. , 1998, Xenobiotica; the fate of foreign compounds in biological systems.

[182]  M. E. Hahn The aryl hydrocarbon receptor: a comparative perspective. , 1998, Comparative biochemistry and physiology. Part C, Pharmacology, toxicology & endocrinology.

[183]  J. Corton,et al.  Interaction of Estrogenic Chemicals and Phytoestrogens with Estrogen Receptor β. , 1998, Endocrinology.

[184]  J. Lehmann,et al.  The human orphan nuclear receptor PXR is activated by compounds that regulate CYP3A4 gene expression and cause drug interactions. , 1998, The Journal of clinical investigation.

[185]  D. Kupfer,et al.  Human cytochrome P450-catalyzed conversion of the proestrogenic pesticide methoxychlor into an estrogen. Role of CYP2C19 and CYP1A2 in O-demethylation. , 1998, Drug metabolism and disposition: the biological fate of chemicals.

[186]  J. Miyamoto,et al.  Environmental exposure, species differences and risk assessment , 1998 .

[187]  K. Gaido,et al.  Inhibition of androgen receptor-dependent transcriptional activity by DDT isomers and methoxychlor in HepG2 human hepatoma cells. , 1998, Toxicology and applied pharmacology.

[188]  D. Kupfer,et al.  Prosubstrates of CYP3A4, the major human hepatic cytochrome P450: transformation into substrates by other P450 isoforms. , 1998, Biochemical pharmacology.

[189]  B. van der Burg,et al.  Interference between Progesterone and Dioxin Signal Transduction Pathways , 1998, The Journal of Biological Chemistry.

[190]  T. Zacharewski,et al.  Identification and assessment of endocrine disruptors: limitations of in vivo and in vitro assays. , 1998, Environmental health perspectives.

[191]  J. Gustafsson,et al.  Characterization of cytochrome P450 enzymes in human breast tissue from reduction mammaplasties. , 1998, The Journal of clinical endocrinology and metabolism.

[192]  J. Gustafsson,et al.  Identification of CYP2A3 as a major cytochrome P450 enzyme in the female peripubertal rat breast. , 1998, Molecular pharmacology.

[193]  D J Rance,et al.  The prediction of human pharmacokinetic parameters from preclinical and in vitro metabolism data. , 1997, The Journal of pharmacology and experimental therapeutics.

[194]  R. Tyl,et al.  Endocrine Screening Methods Workshop report: detection of estrogenic and androgenic hormonal and antihormonal activity for chemicals that act via receptor or steroidogenic enzyme mechanisms. , 1997, Reproductive toxicology.

[195]  S. Dehal,et al.  CYP2D6 catalyzes tamoxifen 4-hydroxylation in human liver. , 1997, Cancer research.

[196]  J. Graham,et al.  Physiological action of progesterone in target tissues. , 1997, Endocrine reviews.

[197]  K. Gaido,et al.  Human exposure to endocrine-active chemicals: hazard assessment problems. , 1997, Regulatory toxicology and pharmacology : RTP.

[198]  C. A. Harris,et al.  The estrogenic activity of phthalate esters in vitro. , 1997, Environmental health perspectives.

[199]  D. Schlenk,et al.  Influence of β-Naphthoflavone and Methoxychlor Pretreatment on the Biotransformation and Estrogenic Activity of Methoxychlor in Channel Catfish (Ictalurus punctatus)☆ , 1997 .

[200]  J. Nicolas,et al.  Engineered cell lines as a tool for monitoring biological activity of hormone analogs. , 1997, Analytical biochemistry.

[201]  T. Penning Molecular endocrinology of hydroxysteroid dehydrogenases. , 1997, Endocrine reviews.

[202]  H. Adlercreutz,et al.  Changes in levels of urinary estrogen metabolites after oral indole-3-carbinol treatment in humans. , 1997, Journal of the National Cancer Institute.

[203]  J. Gustafsson,et al.  Cytochrome P450 in the breast and brain: role in tissue-specific activation of xenobiotics. , 1997, Mutation research.

[204]  Romualdo Benigni,et al.  The Development and Validation of Expert Systems for Predicting Toxicity , 1997 .

[205]  J Ashby,et al.  The rodent uterotrophic assay: critical protocol features, studies with nonyl phenols, and comparison with a yeast estrogenicity assay. , 1997, Regulatory toxicology and pharmacology : RTP.

[206]  P. Bertics,et al.  Regional distribution of cytosolic and particulate 5α-dihydroprogesterone 3α-hydroxysteroid oxidoreductases in female rat brain , 1997, The Journal of Steroid Biochemistry and Molecular Biology.

[207]  D. Kupfer,et al.  Catalytic characteristics of CYP3A4: requirement for a phenolic function in ortho hydroxylation of estradiol and mono-O-demethylated methoxychlor. , 1997, Biochemistry.

[208]  C. Capen,et al.  Mechanistic Data and Risk Assessment of Selected Toxic End Points of the Thyroid Gland , 1997, Toxicologic pathology.

[209]  J R Reel,et al.  Survey and assessment of mammalian estrogen biological assays for hazard characterization. , 1996, Fundamental and applied toxicology : official journal of the Society of Toxicology.

[210]  M D Shelby,et al.  Assessing environmental chemicals for estrogenicity using a combination of in vitro and in vivo assays. , 1996, Environmental health perspectives.

[211]  H. Greim,et al.  Stable expression and coexpression of human cytochrome P450 oxidoreductase and cytochrome P450 1A2 in V79 Chinese hamster cells: sensitivity to quinones and biotransformation of 7-alkoxyresorufins and triazines. , 1996, Drug metabolism and disposition: the biological fate of chemicals.

[212]  N. Weigel Steroid hormone receptors and their regulation by phosphorylation. , 1996, The Biochemical journal.

[213]  T. Zacharewski,et al.  Assessing the estrogenic and dioxin-like activities of chemicals and complex mixtures using in vitro recombinant receptor-reporter gene assays. , 1996, Canadian journal of physiology and pharmacology.

[214]  T. Zacharewski,et al.  Detection of estrogen- and dioxin-like activity in pulp and paper mill black liquor and effluent using in vitro bioassays , 1995 .

[215]  J. Gustafsson,et al.  Developmental and endocrine regulation of P450 isoforms in rat breast. , 1995, Molecular pharmacology.

[216]  D. Davis,et al.  Effects of pesticides on the ratio of 16 alpha/2-hydroxyestrone: a biologic marker of breast cancer risk. , 1995, Environmental health perspectives.

[217]  S. Dehal,et al.  Cytochrome P450 catalyzed covalent binding of methoxychlor to rat hepatic, microsomal iodothyronine 5'-monodeiodinase, type I: does exposure to methoxychlor disrupt thyroid hormone metabolism? , 1995, Archives of biochemistry and biophysics.

[218]  E. Wilson,et al.  Androgen Receptor Antagonist versus Agonist Activities of the Fungicide Vinclozolin Relative to Hydroxyflutamide (*) , 1995, The Journal of Biological Chemistry.

[219]  T. Zacharewski,et al.  Detection of Estrogen- and Dioxin-like Activity in Pulp and Paper Mill Black Liquor and Effluent Using in vitro Recombinant Receptor/Reporter Gene Assays. , 1995, Environmental science & technology.

[220]  A. Atkinson,et al.  In vitro conversion of environmental estrogenic chemical bisphenol A to DNA binding metabolite(s). , 1995, Biochemical and biophysical research communications.

[221]  Gilles Klopman,et al.  META. 1. A Program for the Evaluation of Metabolic Transformation of Chemicals , 1994, J. Chem. Inf. Comput. Sci..

[222]  S. J. Brown,et al.  A Comparison between COMPACT and Hazardexpert Evaluations for 80 Chemicals Tested by the NTP/NCI Rodent Bioassay , 1994 .

[223]  Gilles Klopman,et al.  META. 2. A Dictionary Model of Mammalian Xenobiotic Metabolism , 1994, J. Chem. Inf. Comput. Sci..

[224]  K. Korach,et al.  Anti-estrogen activity in the yeast transcription system: Estrogen receptor mediated agonist response , 1994, Steroids.

[225]  Alan R. Boobis,et al.  The Practical Applicability of Hepatocyte Cultures in Routine Testing , 1994 .

[226]  N. Kerkvliet,et al.  Immunologic and endocrine effects of the flame-retardant pentabromodiphenyl ether (DE-71) in C57BL/6J mice. , 1994, Toxicology.

[227]  D. Kupfer,et al.  Reversible and time-dependent inhibition of the hepatic cytochrome P450 steroidal hydroxylases by the proestrogenic pesticide methoxychlor in rat and human. , 1993, Journal of biochemical toxicology.

[228]  J. Gustafsson,et al.  Role of brain cytochrome P450 in regulation of the level of anesthetic steroids in the brain. , 1993, Molecular pharmacology.

[229]  J. Doehmer V79 Chinese hamster cells genetically engineered for cytochrome P450 and their use in mutagenicity and metabolism studies. , 1993, Toxicology.

[230]  P. Balaguer,et al.  Study of an antiestrogenic effect of retinoic acid in MCF-7 cells. , 1992, Biochemical and biophysical research communications.

[231]  A. Munck,et al.  Phosphorylation of steroid hormone receptors. , 1992, Endocrine reviews.

[232]  H. Murakami,et al.  Progesterone metabolism in recombinant yeast simultaneously expressing bovine cytochromes P450c17 (CYP17A1) and P450c21 (CYP21B1) and yeast NADPH-P450 oxidoreductase. , 1991, Pharmacogenetics.

[233]  C. Ioannides,et al.  The Safety Evaluation of Drugs and Chemicals by the Use of Computer Optimised Molecular Parametric Analysis of Chemical Toxicity (COMPACT) , 1990 .

[234]  D. Kupfer,et al.  Studies on the formation of methoxychlor-protein adduct in rat and human liver microsomes. Is demethylation of methoxychlor essential for cytochrome P450 catalyzed covalent binding? , 1990, Biochemical pharmacology.

[235]  J. Gierthy,et al.  2,3,7,8-Tetrachlorodibenzo-p-dioxin causes an extensive alteration of 17 beta-estradiol metabolism in MCF-7 breast tumor cells. , 1990, Proceedings of the National Academy of Sciences of the United States of America.

[236]  R. Tukey,et al.  Characterization of the CYP2C5 gene in 21L III/J rabbits. Allelic variation affects the expression of P450IIC5. , 1990, The Journal of biological chemistry.

[237]  F. Kadlubar,et al.  Arachidonic acid-dependent peroxidative activation of carcinogenic arylamines by extrahepatic human tissue microsomes. , 1989, Cancer research.

[238]  D. Kupfer,et al.  Metabolic activation of pesticides with proestrogenic activity. , 1987, Federation proceedings.

[239]  K. Netter Progress in drug metabolism , 1985 .

[240]  D. N. Kirk,et al.  Nonsteroidal estrogens of dietary origin: possible roles in hormone-dependent disease. , 1984, The American journal of clinical nutrition.

[241]  R. Muccitelli,et al.  Interactions of methoxychlor, methoxychlor base-soluble contaminant, and 2,2-bis(p-hydroxyphenyl)-1,1,1-trichloroethane with rat uterine estrogen receptor. , 1978, Journal of toxicology and environmental health.

[242]  J. Jenkins,et al.  Metabolism of [14C]testosterone by human foetal and adult brain tissue. , 1977, The Journal of endocrinology.

[243]  B. C. Challis Rapid Nitrosation of Phenols and its Implications for Health Hazards from Dietary Nitrites , 1973, Nature.

[244]  V. Deulofeu [Physiology and pharmacology]. , 1951, Medicina.

[245]  J. Zempleni,et al.  Nuclear receptors and dietary ligands. , 2005 .

[246]  G. Carlson,et al.  Benzene metabolism in human lung cell lines BEAS‐2B and A549 and cells overexpressing CYP2F1 , 2004, Journal of biochemical and molecular toxicology.

[247]  G. Scholz,et al.  Endocrine toxicology--contributions of in vitro methods to the 3R concept. , 2004, ALTEX.

[248]  D. Soprano,et al.  Pharmacological doses of some synthetic retinoids can modulate both the aryl hydrocarbon receptor and retinoid receptor pathways. , 2003, The Journal of nutrition.

[249]  T. Schrader,et al.  Mutagenicity of bisphenol A (4,4'-isopropylidenediphenol) in vitro: effects of nitrosylation. , 2002, Teratogenesis, carcinogenesis, and mutagenesis.

[250]  W. Teubner,et al.  Expression of cytochrome P450 enzymes in human colon. , 2002, IARC scientific publications.

[251]  K. Swales An investigation of host cell effects on the xenobiotic induction of cytochrome P450 3A , 2002 .

[252]  S. Kadota,et al.  Sulfation of environmental estrogens by cytosolic human sulfotransferases. , 2002, Drug metabolism and pharmacokinetics.

[253]  A. Y. Lu,et al.  Interindividual variability in inhibition and induction of cytochrome P450 enzymes. , 2001, Annual review of pharmacology and toxicology.

[254]  J B Houston,et al.  In vitro human tissue models in risk assessment: report of a consensus-building workshop. , 2001, Toxicological sciences : an official journal of the Society of Toxicology.

[255]  M. Gallo,et al.  Regulation of cell cycle and cyclins by 16 -hydroxyestrone in MCF-7 breast cancer cells , 2001 .

[256]  M. Denison,et al.  Recombinant cell bioassays for endocrine disruptors: development of a stably transfected human ovarian cell line for the detection of estrogenic and anti-estrogenic chemicals. , 2000, In vitro & molecular toxicology.

[257]  C. A. Harris,et al.  Issues arising when interpreting results from an in vitro assay for estrogenic activity. , 2000, Toxicology and applied pharmacology.

[258]  N. Vermeulen,et al.  Genetic polymorphisms of human N-acetyltransferase, cytochrome P450, glutathione-S-transferase, and epoxide hydrolase enzymes: relevance to xenobiotic metabolism and toxicity. , 1999, Critical reviews in toxicology.

[259]  P N Judson,et al.  Knowledge-based expert systems for toxicity and metabolism prediction: DEREK, StAR and METEOR. , 1999, SAR and QSAR in environmental research.

[260]  P. Philip,et al.  Use of V79 cells with stably transfected cytochrome P450 cDNAs in studying the metabolism and effects of cytotoxic drugs , 1999, Cancer Chemotherapy and Pharmacology.

[261]  O Pelkonen,et al.  Xenobiotic-metabolizing enzymes and cancer risk: correspondence between genotype and phenotype. , 1999, IARC scientific publications.

[262]  J. Hakkola,et al.  Xenobiotic-metabolizing cytochrome P450 enzymes in the human feto-placental unit: role in intrauterine toxicity. , 1998, Critical reviews in toxicology.

[263]  Y. Sugiyama,et al.  Quantitative prediction of in vivo drug clearance and drug interactions from in vitro data on metabolism, together with binding and transport. , 1998, Annual review of pharmacology and toxicology.

[264]  C. Ioannides,et al.  An improved and updated version of the compact procedure for the evaluation of P450-mediated chemical activation. , 1998, Drug metabolism reviews.

[265]  Worth Andrew,et al.  The Development and Validation of Expert Systems for Predicting Toxicity. , 1998 .

[266]  J. Gustafsson,et al.  Extrahepatic cytochrome P450: role in in situ toxicity and cell-specific hormone sensitivity. , 1998, Archives of toxicology. Supplement. = Archiv fur Toxikologie. Supplement.

[267]  B. Burchell,et al.  The structure and function of the UDP-glucuronosyltransferase gene family. , 1998, Advances in pharmacology.

[268]  D. J. Smith,et al.  The pharmacokinetics, metabolism, and tissue residues of beta-adrenergic agonists in livestock. , 1998, Journal of animal science.

[269]  T. Cresteil Onset of xenobiotic metabolism in children: toxicological implications. , 1998, Food additives and contaminants.

[270]  D. Utesch,et al.  Metabolic activity of fresh and cryopreserved dog hepatocyte suspensions. , 1998, Xenobiotica; the fate of foreign compounds in biological systems.

[271]  H. Bryant,et al.  Hypocholesterolemic activity of raloxifene (LY139481): pharmacological characterization as a selective estrogen receptor modulator. , 1997, The Journal of pharmacology and experimental therapeutics.

[272]  K. Korzekwa,et al.  Role of human hepatic cytochrome P450 1A2 and 3A4 in the metabolic activation of estrone. , 1997, Carcinogenesis.

[273]  J B Houston,et al.  Prediction of hepatic clearance from microsomes, hepatocytes, and liver slices. , 1997, Drug metabolism reviews.

[274]  D. Lewis,et al.  Cytochromes P450: structure, function and mechanism. , 1996 .

[275]  A. Pfeifer,et al.  18 – Drug Metabolism and Carcinogen Activation Studies with Human Genetically Engineered Cells , 1996 .

[276]  R. Combes The in vivo relevance of in vitro genotoxicity assays incorporating enzyme activation systems , 1992 .

[277]  S. Tannenbaum,et al.  The effect of nitrate intake on nitrite formation in human saliva. , 1976, Food and cosmetics toxicology.

[278]  G. Eisenbrand,et al.  Influence of dietary nitrate on nitrite content of human saliva: possible relevance to in vivo formation of N-nitroso compounds. , 1976, Food and cosmetics toxicology.

[279]  J. Bridges,et al.  Progress in drug metabolism , 1976 .

[280]  D. Aviado Physiology and pharmacology , 1965 .

[281]  R. Dorfman Steroid Hormone Metabolism , 1961 .

[282]  K. Korach,et al.  Printed in U.S.A. Copyright © 1997 by The Endocrine Society Estrogenic Activity of a Dieldrin/Toxaphene Mixture in the Mouse Uterus, MCF-7 Human Breast Cancer Cells, and Yeast-Based Estrogen Receptor Assays: No Apparent Synergism* , 2022 .