메뉴 건너뛰기




Volumn 33, Issue 4, 2007, Pages 369-380

The role of nuclear receptors in pharmacokinetic drug-drug interactions in oncology

Author keywords

Anticancer drugs; CYP3A4; Drug drug interactions; Induction; Nuclear receptors; Oncology; PXR

Indexed keywords

7 ETHYL 10 HYDROXYCAMPTOTHECIN; ANALGESIC AGENT; ANASTROZOLE; ANTIEMETIC AGENT; ANTINEOPLASTIC AGENT; CARRIER PROTEIN; CELL NUCLEUS RECEPTOR; CONSTITUTIVE ANDROSTANE RECEPTOR; CYCLOPHOSPHAMIDE; CYTOCHROME P450 2C9; CYTOCHROME P450 3A4; DOCETAXEL; ERLOTINIB; GLUCURONOSYLTRANSFERASE 1A1; GLYCOPROTEIN P; HYPERICUM PERFORATUM EXTRACT; IFOSFAMIDE; IMATINIB; IRINOTECAN; KETOCONAZOLE; LETROZOLE; MULTIDRUG RESISTANCE PROTEIN 1; PACLITAXEL; PHENOBARBITAL; PHENYTOIN; PREGNANE X RECEPTOR; RIFAMPICIN; TAMOXIFEN; UNINDEXED DRUG; VITAMIN D RECEPTOR;

EID: 34248561199     PISSN: 03057372     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ctrv.2007.02.003     Document Type: Review
Times cited : (109)

References (101)
  • 1
    • 0034851464 scopus 로고    scopus 로고
    • Clinical-pharmacological strategies to assess drug interaction potential during drug development
    • Kuhlmann J., and Muck W. Clinical-pharmacological strategies to assess drug interaction potential during drug development. Drug Safety 24 (2001) 715-725
    • (2001) Drug Safety , vol.24 , pp. 715-725
    • Kuhlmann, J.1    Muck, W.2
  • 2
    • 4043179101 scopus 로고    scopus 로고
    • Drug interactions in oncology
    • Beijnen J.H., and Schellens J.H. Drug interactions in oncology. Lancet Oncol 5 (2004) 489-496
    • (2004) Lancet Oncol , vol.5 , pp. 489-496
    • Beijnen, J.H.1    Schellens, J.H.2
  • 3
    • 0033755482 scopus 로고    scopus 로고
    • Drug-drug interactions in medical patients: effects of in-hospital treatment and relation to multiple drug use
    • Kohler G.I., Bode-Boger S.M., Busse R., Hoopmann M., Welte T., and Boger R.H. Drug-drug interactions in medical patients: effects of in-hospital treatment and relation to multiple drug use. Int J Clin Pharmacol Ther 38 (2000) 504-513
    • (2000) Int J Clin Pharmacol Ther , vol.38 , pp. 504-513
    • Kohler, G.I.1    Bode-Boger, S.M.2    Busse, R.3    Hoopmann, M.4    Welte, T.5    Boger, R.H.6
  • 4
    • 2942729844 scopus 로고    scopus 로고
    • Herbal remedies in the United States: potential adverse interactions with anticancer agents
    • Sparreboom A., Cox M.C., Acharya M.R., and Figg W.D. Herbal remedies in the United States: potential adverse interactions with anticancer agents. J Clin Oncol 22 (2004) 2489-2503
    • (2004) J Clin Oncol , vol.22 , pp. 2489-2503
    • Sparreboom, A.1    Cox, M.C.2    Acharya, M.R.3    Figg, W.D.4
  • 5
    • 33746604494 scopus 로고    scopus 로고
    • Herb-drug interactions in oncology: focus on mechanisms of induction
    • Meijerman I., Beijnen J.H., and Schellens J.H. Herb-drug interactions in oncology: focus on mechanisms of induction. Oncologist 11 (2006) 742-752
    • (2006) Oncologist , vol.11 , pp. 742-752
    • Meijerman, I.1    Beijnen, J.H.2    Schellens, J.H.3
  • 6
    • 0032742241 scopus 로고    scopus 로고
    • Cancer chemotherapy: the promise and the pitfalls
    • McLeod H.L.E., and Oral W.E. Cancer chemotherapy: the promise and the pitfalls. Clin Cancer Res 5 (1999) 2669-2671
    • (1999) Clin Cancer Res , vol.5 , pp. 2669-2671
    • McLeod, H.L.E.1    Oral, W.E.2
  • 9
    • 34248536151 scopus 로고    scopus 로고
    • Product info of erlotinib. http://www.gene.com/gene/products/information/oncology/tarceva/insert.jsp.
  • 10
    • 0024533623 scopus 로고
    • Oxidative metabolism of cyclophosphamide: identification of the hepatic monooxygenase catalysts of drug activation
    • Clarke L., and Waxman D.J. Oxidative metabolism of cyclophosphamide: identification of the hepatic monooxygenase catalysts of drug activation. Cancer Res 49 (1989) 2344-2350
    • (1989) Cancer Res , vol.49 , pp. 2344-2350
    • Clarke, L.1    Waxman, D.J.2
  • 12
    • 0032498303 scopus 로고    scopus 로고
    • An orphan nuclear receptor activated by pregnanes defines a novel steroid signaling pathway
    • Kliewer S.A., Moore J.T., Wade L., Staudinger J.L., Watson M.A., Jones S.A., et al. An orphan nuclear receptor activated by pregnanes defines a novel steroid signaling pathway. Cell 92 (1998) 73-82
    • (1998) Cell , vol.92 , pp. 73-82
    • Kliewer, S.A.1    Moore, J.T.2    Wade, L.3    Staudinger, J.L.4    Watson, M.A.5    Jones, S.A.6
  • 13
    • 0028210426 scopus 로고
    • A new orphan member of the nuclear hormone receptor superfamily that interacts with a subset of retinoic acid response elements
    • Baes M., Gulick T., Choi H.S., Martinoli M.G., Simha D., and Moore D.D. A new orphan member of the nuclear hormone receptor superfamily that interacts with a subset of retinoic acid response elements. Mol Cell Biol 14 (1994) 1544-1552
    • (1994) Mol Cell Biol , vol.14 , pp. 1544-1552
    • Baes, M.1    Gulick, T.2    Choi, H.S.3    Martinoli, M.G.4    Simha, D.5    Moore, D.D.6
  • 14
    • 0032169485 scopus 로고    scopus 로고
    • The human orphan nuclear receptor PXR is activated by compounds that regulate CYP3A4 gene expression and cause drug interactions
    • Lehmann J.M., McKee D.D., Watson M.A., Willson T.M., Moore J.T., and Kliewer S.A. The human orphan nuclear receptor PXR is activated by compounds that regulate CYP3A4 gene expression and cause drug interactions. J Clin Invest 102 (1998) 1016-1023
    • (1998) J Clin Invest , vol.102 , pp. 1016-1023
    • Lehmann, J.M.1    McKee, D.D.2    Watson, M.A.3    Willson, T.M.4    Moore, J.T.5    Kliewer, S.A.6
  • 15
    • 0035038919 scopus 로고    scopus 로고
    • The orphan nuclear receptor SXR coordinately regulates drug metabolism and efflux
    • Synold T.W., Dussault I., and Forman B.M. The orphan nuclear receptor SXR coordinately regulates drug metabolism and efflux. Nat Med 7 (2001) 584-590
    • (2001) Nat Med , vol.7 , pp. 584-590
    • Synold, T.W.1    Dussault, I.2    Forman, B.M.3
  • 16
    • 23144459452 scopus 로고    scopus 로고
    • Animal models of xenobiotic receptors
    • Dai G., and Wan Y.J. Animal models of xenobiotic receptors. Curr Drug Metab 6 (2005) 341-355
    • (2005) Curr Drug Metab , vol.6 , pp. 341-355
    • Dai, G.1    Wan, Y.J.2
  • 17
    • 0036765785 scopus 로고    scopus 로고
    • Nuclear pregnane X receptor and constitutive androstane receptor regulate overlapping but distinct sets of genes involved in xenobiotic detoxification
    • Maglich J.M., Stoltz C.M., Goodwin B., Hawkins-Brown D., Moore J.T., and Kliewer S.A. Nuclear pregnane X receptor and constitutive androstane receptor regulate overlapping but distinct sets of genes involved in xenobiotic detoxification. Mol Pharmacol 62 (2002) 638-646
    • (2002) Mol Pharmacol , vol.62 , pp. 638-646
    • Maglich, J.M.1    Stoltz, C.M.2    Goodwin, B.3    Hawkins-Brown, D.4    Moore, J.T.5    Kliewer, S.A.6
  • 18
    • 33751541421 scopus 로고    scopus 로고
    • Phenytoin induction of the Cyp2c37 gene is mediated by the constitutive androstane receptor
    • Jackson J.P., Ferguson S.S., Negishi M., and Goldstein J.A. Phenytoin induction of the Cyp2c37 gene is mediated by the constitutive androstane receptor. Drug Metab Dispos (2006)
    • (2006) Drug Metab Dispos
    • Jackson, J.P.1    Ferguson, S.S.2    Negishi, M.3    Goldstein, J.A.4
  • 19
    • 0038650987 scopus 로고    scopus 로고
    • Nuclear receptor, pregname X receptor, is required for induction of UDP-glucuronosyltranferases in mouse liver by pregnenolone-16 alpha-carbonitrile
    • Chen C., Staudinger J.L., and Klaassen C.D. Nuclear receptor, pregname X receptor, is required for induction of UDP-glucuronosyltranferases in mouse liver by pregnenolone-16 alpha-carbonitrile. Drug Metab Dispos 31 (2003) 908-915
    • (2003) Drug Metab Dispos , vol.31 , pp. 908-915
    • Chen, C.1    Staudinger, J.L.2    Klaassen, C.D.3
  • 20
    • 17744375160 scopus 로고    scopus 로고
    • The pregnane X receptor: a promiscuous xenobiotic receptor that has diverged during evolution
    • Jones S.A., Moore L.B., Shenk J.L., Wisely G.B., Hamilton G.A., McKee D.D., et al. The pregnane X receptor: a promiscuous xenobiotic receptor that has diverged during evolution. Mol Endocrinol 14 (2000) 27-39
    • (2000) Mol Endocrinol , vol.14 , pp. 27-39
    • Jones, S.A.1    Moore, L.B.2    Shenk, J.L.3    Wisely, G.B.4    Hamilton, G.A.5    McKee, D.D.6
  • 21
    • 0034721159 scopus 로고    scopus 로고
    • Humanized xenobiotic response in mice expressing nuclear receptor SXR
    • Xie W., Barwick J.L., Downes M., Blumberg B., Simon C.M., Nelson M.C., et al. Humanized xenobiotic response in mice expressing nuclear receptor SXR. Nature 406 (2000) 435-439
    • (2000) Nature , vol.406 , pp. 435-439
    • Xie, W.1    Barwick, J.L.2    Downes, M.3    Blumberg, B.4    Simon, C.M.5    Nelson, M.C.6
  • 22
    • 33748950454 scopus 로고    scopus 로고
    • In vivo activation of human pregnane X receptor tightens the blood-brain barrier to methadone through P-glycoprotein up-regulation
    • Bauer B., Yang X., Hartz A.M., Olson E.R., Zhao R., Kalvass J.C., et al. In vivo activation of human pregnane X receptor tightens the blood-brain barrier to methadone through P-glycoprotein up-regulation. Mol Pharmacol 70 (2006) 1212-1219
    • (2006) Mol Pharmacol , vol.70 , pp. 1212-1219
    • Bauer, B.1    Yang, X.2    Hartz, A.M.3    Olson, E.R.4    Zhao, R.5    Kalvass, J.C.6
  • 23
    • 0034874393 scopus 로고    scopus 로고
    • Regulation of the human CYP2B6 gene by the nuclear pregnane X receptor
    • Goodwin B., Moore L.B., Stoltz C.M., McKee D.D., and Kliewer S.A. Regulation of the human CYP2B6 gene by the nuclear pregnane X receptor. Mol Pharmacol 60 (2001) 427-431
    • (2001) Mol Pharmacol , vol.60 , pp. 427-431
    • Goodwin, B.1    Moore, L.B.2    Stoltz, C.M.3    McKee, D.D.4    Kliewer, S.A.5
  • 24
    • 23944516070 scopus 로고    scopus 로고
    • Human CYP2C8 is transcriptionally regulated by the nuclear receptors constitutive androstane receptor, pregnane X receptor, glucocorticoid receptor, and hepatic nuclear factor 4alpha
    • Ferguson S.S., Chen Y., LeCluyse E.L., Negishi M., and Goldstein J.A. Human CYP2C8 is transcriptionally regulated by the nuclear receptors constitutive androstane receptor, pregnane X receptor, glucocorticoid receptor, and hepatic nuclear factor 4alpha. Mol Pharmacol 68 (2005) 747-757
    • (2005) Mol Pharmacol , vol.68 , pp. 747-757
    • Ferguson, S.S.1    Chen, Y.2    LeCluyse, E.L.3    Negishi, M.4    Goldstein, J.A.5
  • 25
    • 1642498178 scopus 로고    scopus 로고
    • Induction of human CYP2C9 by rifampicin, hyperforin, and phenobarbital is mediated by the pregnane X receptor
    • Chen Y., Ferguson S.S., Negishi M., and Goldstein J.A. Induction of human CYP2C9 by rifampicin, hyperforin, and phenobarbital is mediated by the pregnane X receptor. J Pharmacol Exp Ther 308 (2004) 495-501
    • (2004) J Pharmacol Exp Ther , vol.308 , pp. 495-501
    • Chen, Y.1    Ferguson, S.S.2    Negishi, M.3    Goldstein, J.A.4
  • 27
    • 0037386735 scopus 로고    scopus 로고
    • Control of steroid, heme, and carcinogen metabolism by nuclear pregnane X receptor and constitutive androstane receptor
    • Xie W., Yeuh M.F., Radominska-Pandya A., Saini S.P., Negishi Y., Bottroff B.S., et al. Control of steroid, heme, and carcinogen metabolism by nuclear pregnane X receptor and constitutive androstane receptor. Proc Natl Acad Sci USA 100 (2003) 4150-4155
    • (2003) Proc Natl Acad Sci USA , vol.100 , pp. 4150-4155
    • Xie, W.1    Yeuh, M.F.2    Radominska-Pandya, A.3    Saini, S.P.4    Negishi, Y.5    Bottroff, B.S.6
  • 28
    • 0037169551 scopus 로고    scopus 로고
    • Regulation of multidrug resistance-associated protein 2 (ABCC2) by the nuclear receptors pregnane X receptor, farnesoid X-activated receptor, and constitutive androstane receptor
    • Kast H.R., Goodwin B., Tarr P.T., Jones S.A., Anisfeld A.M., Stoltz C.M., et al. Regulation of multidrug resistance-associated protein 2 (ABCC2) by the nuclear receptors pregnane X receptor, farnesoid X-activated receptor, and constitutive androstane receptor. J Biol Chem 277 (2002) 2908-2915
    • (2002) J Biol Chem , vol.277 , pp. 2908-2915
    • Kast, H.R.1    Goodwin, B.2    Tarr, P.T.3    Jones, S.A.4    Anisfeld, A.M.5    Stoltz, C.M.6
  • 29
    • 6344266966 scopus 로고    scopus 로고
    • Expression of constitutive androstane receptor splice variants in human tissues and their functional consequences
    • Lamba J.K., Lamba V., Yasuda K., Lin Y.S., Assem M., Thompson E., et al. Expression of constitutive androstane receptor splice variants in human tissues and their functional consequences. J Pharmacol Exp Ther 311 (2004) 811-821
    • (2004) J Pharmacol Exp Ther , vol.311 , pp. 811-821
    • Lamba, J.K.1    Lamba, V.2    Yasuda, K.3    Lin, Y.S.4    Assem, M.5    Thompson, E.6
  • 30
    • 0031682988 scopus 로고    scopus 로고
    • The nuclear orphan receptor CAR-retinoid X receptor heterodimer activates the phenobarbital-responsive enhancer module of the CYP2B gene
    • Honkakoski P., Zelko I., Sueyoshi T., and Negishi M. The nuclear orphan receptor CAR-retinoid X receptor heterodimer activates the phenobarbital-responsive enhancer module of the CYP2B gene. Mol Cell Biol 18 (1998) 5652-5658
    • (1998) Mol Cell Biol , vol.18 , pp. 5652-5658
    • Honkakoski, P.1    Zelko, I.2    Sueyoshi, T.3    Negishi, M.4
  • 31
    • 0032766430 scopus 로고    scopus 로고
    • Phenobarbital-responsive nuclear translocation of the receptor CAR in induction of the CYP2B gene
    • Kawamoto T., Sueyoshi T., Zelko I., Moore R., Washburn K., and Negishi M. Phenobarbital-responsive nuclear translocation of the receptor CAR in induction of the CYP2B gene. Mol Cell Biol 19 (1999) 6318-6322
    • (1999) Mol Cell Biol , vol.19 , pp. 6318-6322
    • Kawamoto, T.1    Sueyoshi, T.2    Zelko, I.3    Moore, R.4    Washburn, K.5    Negishi, M.6
  • 32
    • 0042236405 scopus 로고    scopus 로고
    • Identification of the nuclear receptor CAR:HSP90 complex in mouse liver and recruitment of protein phosphatase 2A in response to phenobarbital
    • Yoshinari K., Kobayashi K., Moore R., Kawamoto T., and Negishi M. Identification of the nuclear receptor CAR:HSP90 complex in mouse liver and recruitment of protein phosphatase 2A in response to phenobarbital. FEBS Lett 548 (2003) 17-20
    • (2003) FEBS Lett , vol.548 , pp. 17-20
    • Yoshinari, K.1    Kobayashi, K.2    Moore, R.3    Kawamoto, T.4    Negishi, M.5
  • 33
    • 0037931737 scopus 로고    scopus 로고
    • Identification of a novel human constitutive androstane receptor (CAR) agonist and its use in the identification of CAR target genes
    • Maglich J.M., Parks D.J., Moore L.B., Collins J.L., Goodwin B., Billin A.N., et al. Identification of a novel human constitutive androstane receptor (CAR) agonist and its use in the identification of CAR target genes. J Biol Chem 278 (2003) 17277-17283
    • (2003) J Biol Chem , vol.278 , pp. 17277-17283
    • Maglich, J.M.1    Parks, D.J.2    Moore, L.B.3    Collins, J.L.4    Goodwin, B.5    Billin, A.N.6
  • 34
    • 0037389946 scopus 로고    scopus 로고
    • Induction of bilirubin clearance by the constitutive androstane receptor (CAR)
    • Huang W., Zhang J., Chua S.S., Qatanani M., Han Y., Granata R., et al. Induction of bilirubin clearance by the constitutive androstane receptor (CAR). Proc Natl Acad Sci USA 100 (2003) 4156-4161
    • (2003) Proc Natl Acad Sci USA , vol.100 , pp. 4156-4161
    • Huang, W.1    Zhang, J.2    Chua, S.S.3    Qatanani, M.4    Han, Y.5    Granata, R.6
  • 35
    • 0036765751 scopus 로고    scopus 로고
    • Regulation of human CYP2C9 by the constitutive androstane receptor: discovery of a new distal binding site
    • Ferguson S.S., LeCluyse E.L., Negishi M., and Goldstein J.A. Regulation of human CYP2C9 by the constitutive androstane receptor: discovery of a new distal binding site. Mol Pharmacol 62 (2002) 737-746
    • (2002) Mol Pharmacol , vol.62 , pp. 737-746
    • Ferguson, S.S.1    LeCluyse, E.L.2    Negishi, M.3    Goldstein, J.A.4
  • 36
    • 0042844649 scopus 로고    scopus 로고
    • Identification of constitutive androstane receptor and glucocorticoid receptor binding sites in the CYP2C19 promoter
    • Chen Y., Ferguson S.S., Negishi M., and Goldstein J.A. Identification of constitutive androstane receptor and glucocorticoid receptor binding sites in the CYP2C19 promoter. Mol Pharmacol 64 (2003) 316-324
    • (2003) Mol Pharmacol , vol.64 , pp. 316-324
    • Chen, Y.1    Ferguson, S.S.2    Negishi, M.3    Goldstein, J.A.4
  • 37
    • 0036070955 scopus 로고    scopus 로고
    • Transcriptional regulation of the human CYP3A4 gene by the constitutive androstane receptor
    • Goodwin B., Hodgson E., D'Costa D.J., Robertson G.R., and Liddle C. Transcriptional regulation of the human CYP3A4 gene by the constitutive androstane receptor. Mol Pharmacol 62 (2002) 359-365
    • (2002) Mol Pharmacol , vol.62 , pp. 359-365
    • Goodwin, B.1    Hodgson, E.2    D'Costa, D.J.3    Robertson, G.R.4    Liddle, C.5
  • 38
    • 0035029401 scopus 로고    scopus 로고
    • The phenobarbital response enhancer module in the human bilirubin UDP-glucuronosyltransferase UGT1A1 gene and regulation by the nuclear receptor CAR
    • Sugatani J., Kojima H., Ueda A., Kakizaki S., Yoshinari K., Gong Q.H., et al. The phenobarbital response enhancer module in the human bilirubin UDP-glucuronosyltransferase UGT1A1 gene and regulation by the nuclear receptor CAR. Hepatology 33 (2001) 1232-1238
    • (2001) Hepatology , vol.33 , pp. 1232-1238
    • Sugatani, J.1    Kojima, H.2    Ueda, A.3    Kakizaki, S.4    Yoshinari, K.5    Gong, Q.H.6
  • 39
    • 9144231188 scopus 로고    scopus 로고
    • A novel constitutive androstane receptor-mediated and CYP3A-independent pathway of bile acid detoxification
    • Saini S.P., Sonoda J., Xu L., Toma D., Uppal H., Mu Y., et al. A novel constitutive androstane receptor-mediated and CYP3A-independent pathway of bile acid detoxification. Mol Pharmacol 65 (2004) 292-300
    • (2004) Mol Pharmacol , vol.65 , pp. 292-300
    • Saini, S.P.1    Sonoda, J.2    Xu, L.3    Toma, D.4    Uppal, H.5    Mu, Y.6
  • 40
    • 26844549175 scopus 로고    scopus 로고
    • A role for constitutive androstane receptor in the regulation of human intestinal MDR1 expression
    • Burk O., Arnold K.A., Geick A., Tegude H., and Eichelbaum M. A role for constitutive androstane receptor in the regulation of human intestinal MDR1 expression. Biol Chem 386 (2005) 503-513
    • (2005) Biol Chem , vol.386 , pp. 503-513
    • Burk, O.1    Arnold, K.A.2    Geick, A.3    Tegude, H.4    Eichelbaum, M.5
  • 41
    • 0043168030 scopus 로고    scopus 로고
    • Coactivator binding promotes the specific interaction between ligand and the pregnane X receptor
    • Watkins R.E., Davis-Searles P.R., Lambert M.H., and Redinbo M.R. Coactivator binding promotes the specific interaction between ligand and the pregnane X receptor. J Mol Biol 331 (2003) 815-828
    • (2003) J Mol Biol , vol.331 , pp. 815-828
    • Watkins, R.E.1    Davis-Searles, P.R.2    Lambert, M.H.3    Redinbo, M.R.4
  • 42
    • 0033400343 scopus 로고    scopus 로고
    • Nuclear receptors: coactivators, corepressors and chromatin remodeling in the control of transcription
    • Collingwood T.N., Urnov F.D., and Wolffe A.P. Nuclear receptors: coactivators, corepressors and chromatin remodeling in the control of transcription. J Mol Endocrinol 23 (1999) 255-275
    • (1999) J Mol Endocrinol , vol.23 , pp. 255-275
    • Collingwood, T.N.1    Urnov, F.D.2    Wolffe, A.P.3
  • 43
    • 0035038008 scopus 로고    scopus 로고
    • Phenobarbital response elements of cytochrome P450 genes and nuclear receptors
    • Sueyoshi T., and Negishi M. Phenobarbital response elements of cytochrome P450 genes and nuclear receptors. Annu Rev Pharmacol Toxicol 41 (2001) 123-143
    • (2001) Annu Rev Pharmacol Toxicol , vol.41 , pp. 123-143
    • Sueyoshi, T.1    Negishi, M.2
  • 44
    • 0033638960 scopus 로고    scopus 로고
    • Reciprocal activation of xenobiotic response genes by nuclear receptors SXR/PXR and CAR
    • Xie W., Barwick J.L., Simon C.M., Pierce A.M., Safe S., Blumberg B., et al. Reciprocal activation of xenobiotic response genes by nuclear receptors SXR/PXR and CAR. Genes Dev 14 (2000) 3014-3023
    • (2000) Genes Dev , vol.14 , pp. 3014-3023
    • Xie, W.1    Barwick, J.L.2    Simon, C.M.3    Pierce, A.M.4    Safe, S.5    Blumberg, B.6
  • 45
    • 0035206829 scopus 로고    scopus 로고
    • Transcriptional control of intestinal cytochrome P-4503A by 1alpha,25-dihydroxy vitamin D3
    • Thummel K.E., Brimer C., Yasuda K., Thottassery J., Senn T., Lin Y., et al. Transcriptional control of intestinal cytochrome P-4503A by 1alpha,25-dihydroxy vitamin D3. Mol Pharmacol 60 (2001) 1399-1406
    • (2001) Mol Pharmacol , vol.60 , pp. 1399-1406
    • Thummel, K.E.1    Brimer, C.2    Yasuda, K.3    Thottassery, J.4    Senn, T.5    Lin, Y.6
  • 46
    • 0037067665 scopus 로고    scopus 로고
    • Expression of CYP3A4, CYP2B6, and CYP2C9 is regulated by the vitamin D receptor pathway in primary human hepatocytes
    • Drocourt L., Ourlin J.C., Pascussi J.M., Maurel P., and Vilarem M.J. Expression of CYP3A4, CYP2B6, and CYP2C9 is regulated by the vitamin D receptor pathway in primary human hepatocytes. J Biol Chem 277 (2002) 25125-25132
    • (2002) J Biol Chem , vol.277 , pp. 25125-25132
    • Drocourt, L.1    Ourlin, J.C.2    Pascussi, J.M.3    Maurel, P.4    Vilarem, M.J.5
  • 47
    • 0030945754 scopus 로고    scopus 로고
    • Expression of enzymatically active CYP3A4 by Caco-2 cells grown on extracellular matrix-coated permeable supports in the presence of 1alpha,25-dihydroxyvitamin D3
    • Schmiedlin-Ren P., Thummel K.E., Fisher J.M., Paine M.F., Lown K.S., and Watkins P.B. Expression of enzymatically active CYP3A4 by Caco-2 cells grown on extracellular matrix-coated permeable supports in the presence of 1alpha,25-dihydroxyvitamin D3. Mol Pharmacol 51 (1997) 741-754
    • (1997) Mol Pharmacol , vol.51 , pp. 741-754
    • Schmiedlin-Ren, P.1    Thummel, K.E.2    Fisher, J.M.3    Paine, M.F.4    Lown, K.S.5    Watkins, P.B.6
  • 50
    • 6944234902 scopus 로고    scopus 로고
    • Regulation of CYP3A4 by the bile acid receptor FXR: evidence for functional binding sites in the CYP3A4 gene
    • Gnerre C., Blattler S., Kaufmann M.R., Looser R., and Meyer U.A. Regulation of CYP3A4 by the bile acid receptor FXR: evidence for functional binding sites in the CYP3A4 gene. Pharmacogenetics 14 (2004) 635-645
    • (2004) Pharmacogenetics , vol.14 , pp. 635-645
    • Gnerre, C.1    Blattler, S.2    Kaufmann, M.R.3    Looser, R.4    Meyer, U.A.5
  • 51
    • 0037119454 scopus 로고    scopus 로고
    • Cholesterol and bile acids regulate xenosensor signaling in drug-mediated induction of cytochromes P450
    • Handschin C., Podvinec M., Amherd R., Looser R., Ourlin J.C., and Meyer U.A. Cholesterol and bile acids regulate xenosensor signaling in drug-mediated induction of cytochromes P450. J Biol Chem 277 (2002) 29561-29567
    • (2002) J Biol Chem , vol.277 , pp. 29561-29567
    • Handschin, C.1    Podvinec, M.2    Amherd, R.3    Looser, R.4    Ourlin, J.C.5    Meyer, U.A.6
  • 52
    • 33745830106 scopus 로고    scopus 로고
    • Pregnane X receptor is a target of farnesoid X receptor
    • Jung D., Mangelsdorf D.J., and Meyer U.A. Pregnane X receptor is a target of farnesoid X receptor. J Biol Chem 281 (2006) 19081-19091
    • (2006) J Biol Chem , vol.281 , pp. 19081-19091
    • Jung, D.1    Mangelsdorf, D.J.2    Meyer, U.A.3
  • 53
    • 0033931266 scopus 로고    scopus 로고
    • Dexamethasone induces pregnane X receptor and retinoid X receptor-alpha expression in human hepatocytes: synergistic increase of CYP3A4 induction by pregnane X receptor activators
    • Pascussi J.M., Drocourt L., Fabre J.M., Maurel P., and Vilarem M.J. Dexamethasone induces pregnane X receptor and retinoid X receptor-alpha expression in human hepatocytes: synergistic increase of CYP3A4 induction by pregnane X receptor activators. Mol Pharmacol 58 (2000) 361-372
    • (2000) Mol Pharmacol , vol.58 , pp. 361-372
    • Pascussi, J.M.1    Drocourt, L.2    Fabre, J.M.3    Maurel, P.4    Vilarem, M.J.5
  • 54
    • 0035659943 scopus 로고    scopus 로고
    • Dual effect of dexamethasone on CYP3A4 gene expression in human hepatocytes. Sequential role of glucocorticoid receptor and pregnane X receptor
    • Pascussi J.M., Drocourt L., Gerbal-Chaloin S., Fabre J.M., Maurel P., and Vilarem M.J. Dual effect of dexamethasone on CYP3A4 gene expression in human hepatocytes. Sequential role of glucocorticoid receptor and pregnane X receptor. Eur J Biochem 268 (2001) 6346-6358
    • (2001) Eur J Biochem , vol.268 , pp. 6346-6358
    • Pascussi, J.M.1    Drocourt, L.2    Gerbal-Chaloin, S.3    Fabre, J.M.4    Maurel, P.5    Vilarem, M.J.6
  • 55
    • 0035124052 scopus 로고    scopus 로고
    • Cytochrome P450 regulation by hepatocyte nuclear factor 4 in human hepatocytes: a study using adenovirus-mediated antisense targeting
    • Jover R., Bort R., Gomez-Lechon M.J., and Castell J.V. Cytochrome P450 regulation by hepatocyte nuclear factor 4 in human hepatocytes: a study using adenovirus-mediated antisense targeting. Hepatology 33 (2001) 668-675
    • (2001) Hepatology , vol.33 , pp. 668-675
    • Jover, R.1    Bort, R.2    Gomez-Lechon, M.J.3    Castell, J.V.4
  • 56
    • 23944510035 scopus 로고    scopus 로고
    • The nuclear receptors constitutive androstane receptor and pregnane X receptor cross-talk with hepatic nuclear factor 4alpha to synergistically activate the human CYP2C9 promoter
    • Chen Y., Kissling G., Negishi M., and Goldstein J.A. The nuclear receptors constitutive androstane receptor and pregnane X receptor cross-talk with hepatic nuclear factor 4alpha to synergistically activate the human CYP2C9 promoter. J Pharmacol Exp Ther 314 (2005) 1125-1133
    • (2005) J Pharmacol Exp Ther , vol.314 , pp. 1125-1133
    • Chen, Y.1    Kissling, G.2    Negishi, M.3    Goldstein, J.A.4
  • 57
    • 0038278508 scopus 로고    scopus 로고
    • An update on in vitro test methods in human hepatic drug biotransformation research: pros and cons
    • Brandon E.F., Raap C.D., Meijerman I., Beijnen J.H., and Schellens J.H. An update on in vitro test methods in human hepatic drug biotransformation research: pros and cons. Toxicol Appl Pharmacol 189 (2003) 233-246
    • (2003) Toxicol Appl Pharmacol , vol.189 , pp. 233-246
    • Brandon, E.F.1    Raap, C.D.2    Meijerman, I.3    Beijnen, J.H.4    Schellens, J.H.5
  • 58
    • 2642674399 scopus 로고    scopus 로고
    • Development of an in vitro reporter gene assay to assess xenobiotic induction of the human CYP3A4 gene
    • Ogg M.S., Gray T.J., and Gibson G.G. Development of an in vitro reporter gene assay to assess xenobiotic induction of the human CYP3A4 gene. Eur J Drug Metab Pharmacokinet 22 (1997) 311-313
    • (1997) Eur J Drug Metab Pharmacokinet , vol.22 , pp. 311-313
    • Ogg, M.S.1    Gray, T.J.2    Gibson, G.G.3
  • 60
    • 8844286879 scopus 로고    scopus 로고
    • CYP3A4 induction by xenobiotics: biochemistry, experimental methods and impact on drug discovery and development
    • Luo G., Guenthner T., Gan L.S., and Humphreys W.G. CYP3A4 induction by xenobiotics: biochemistry, experimental methods and impact on drug discovery and development. Curr Drug Metab 5 (2004) 483-505
    • (2004) Curr Drug Metab , vol.5 , pp. 483-505
    • Luo, G.1    Guenthner, T.2    Gan, L.S.3    Humphreys, W.G.4
  • 61
    • 32244447844 scopus 로고    scopus 로고
    • Evaluation of human liver slices and reporter gene assays as systems for predicting the cytochrome p450 induction potential of drugs in vivo in humans
    • Persson K.P., Ekehed S., Otter C., Lutz E.S., McPheat J., Masimirembwa C.M., et al. Evaluation of human liver slices and reporter gene assays as systems for predicting the cytochrome p450 induction potential of drugs in vivo in humans. Pharm Res 23 (2006) 56-69
    • (2006) Pharm Res , vol.23 , pp. 56-69
    • Persson, K.P.1    Ekehed, S.2    Otter, C.3    Lutz, E.S.4    McPheat, J.5    Masimirembwa, C.M.6
  • 62
    • 22344439421 scopus 로고    scopus 로고
    • Identification of HMG-CoA reductase inhibitors as activators for human, mouse and rat constitutive androstane receptor
    • Kobayashi K., Yamanaka Y., Iwazaki N., Nakajo I., Hosokawa M., Negishi M., et al. Identification of HMG-CoA reductase inhibitors as activators for human, mouse and rat constitutive androstane receptor. Drug Metab Dispos 33 (2005) 924-929
    • (2005) Drug Metab Dispos , vol.33 , pp. 924-929
    • Kobayashi, K.1    Yamanaka, Y.2    Iwazaki, N.3    Nakajo, I.4    Hosokawa, M.5    Negishi, M.6
  • 64
    • 1342344703 scopus 로고    scopus 로고
    • Human PXR variants and their differential effects on the regulation of human UDP-glucuronosyltransferase gene expression
    • Gardner-Stephen D., Heydel J.M., Goyal A., Lu Y., Xie W., Lindblom T., et al. Human PXR variants and their differential effects on the regulation of human UDP-glucuronosyltransferase gene expression. Drug Metab Dispos 32 (2004) 340-347
    • (2004) Drug Metab Dispos , vol.32 , pp. 340-347
    • Gardner-Stephen, D.1    Heydel, J.M.2    Goyal, A.3    Lu, Y.4    Xie, W.5    Lindblom, T.6
  • 65
    • 0036021113 scopus 로고    scopus 로고
    • The drug efflux pump MRP2: regulation of expression in physiopathological situations and by endogenous and exogenous compounds
    • Payen L., Sparfel L., Courtois A., Vernhet L., Guillouzo A., and Fardel O. The drug efflux pump MRP2: regulation of expression in physiopathological situations and by endogenous and exogenous compounds. Cell Biol Toxicol 18 (2002) 221-233
    • (2002) Cell Biol Toxicol , vol.18 , pp. 221-233
    • Payen, L.1    Sparfel, L.2    Courtois, A.3    Vernhet, L.4    Guillouzo, A.5    Fardel, O.6
  • 66
    • 33644505139 scopus 로고    scopus 로고
    • Intestinal expression of P-glycoprotein (ABCB1), multidrug resistance associated protein 2 (ABCC2), and uridine diphosphate-glucuronosyltransferase 1A1 predicts the disposition and modulates the effects of the cholesterol absorption inhibitor ezetimibe in humans
    • Oswald S., Haenisch S., Fricke C., Sudhop T., Remmler C., Giessmann T., et al. Intestinal expression of P-glycoprotein (ABCB1), multidrug resistance associated protein 2 (ABCC2), and uridine diphosphate-glucuronosyltransferase 1A1 predicts the disposition and modulates the effects of the cholesterol absorption inhibitor ezetimibe in humans. Clin Pharmacol Ther 79 (2006) 206-217
    • (2006) Clin Pharmacol Ther , vol.79 , pp. 206-217
    • Oswald, S.1    Haenisch, S.2    Fricke, C.3    Sudhop, T.4    Remmler, C.5    Giessmann, T.6
  • 67
    • 0016245363 scopus 로고
    • Interaction of sodium warfarin and rifampin. Studies in man
    • O'Reilly R.A. Interaction of sodium warfarin and rifampin. Studies in man. Ann Intern Med 81 (1974) 337-340
    • (1974) Ann Intern Med , vol.81 , pp. 337-340
    • O'Reilly, R.A.1
  • 68
    • 0036194775 scopus 로고    scopus 로고
    • Intravenous cyclosporine-rifampin interaction in a pediatric bone marrow transplant recipient
    • Zelunka E.J. Intravenous cyclosporine-rifampin interaction in a pediatric bone marrow transplant recipient. Pharmacotherapy 22 (2002) 387-390
    • (2002) Pharmacotherapy , vol.22 , pp. 387-390
    • Zelunka, E.J.1
  • 69
    • 33644843888 scopus 로고    scopus 로고
    • Roles of rifampicin in drug-drug interactions: underlying molecular mechanisms involving the nuclear pregnane X receptor
    • Chen J., and Raymond K. Roles of rifampicin in drug-drug interactions: underlying molecular mechanisms involving the nuclear pregnane X receptor. Ann Clin Microbiol Antimicrob 5 (2006) 3
    • (2006) Ann Clin Microbiol Antimicrob , vol.5 , pp. 3
    • Chen, J.1    Raymond, K.2
  • 71
    • 0442313672 scopus 로고    scopus 로고
    • Effect of rifampicin on the pharmacokinetics of imatinib mesylate (Gleevec, STI571) in healthy subjects
    • Bolton A.E., Peng B., Hubert M., Krebs-Brown A., Capdeville R., Keller U., et al. Effect of rifampicin on the pharmacokinetics of imatinib mesylate (Gleevec, STI571) in healthy subjects. Cancer Chemother Pharmacol 53 (2004) 102-106
    • (2004) Cancer Chemother Pharmacol , vol.53 , pp. 102-106
    • Bolton, A.E.1    Peng, B.2    Hubert, M.3    Krebs-Brown, A.4    Capdeville, R.5    Keller, U.6
  • 73
    • 7044245637 scopus 로고    scopus 로고
    • The influence of St. John's wort on the pharmacokinetics and protein binding of imatinib mesylate
    • Smith P., Bullock J.M., Booker B.M., Haas C.E., Berenson C.S., and Jusko W.J. The influence of St. John's wort on the pharmacokinetics and protein binding of imatinib mesylate. Pharmacotherapy 24 (2004) 1508-1514
    • (2004) Pharmacotherapy , vol.24 , pp. 1508-1514
    • Smith, P.1    Bullock, J.M.2    Booker, B.M.3    Haas, C.E.4    Berenson, C.S.5    Jusko, W.J.6
  • 77
    • 0031801368 scopus 로고    scopus 로고
    • Phase I study of paclitaxel in patients with recurrent malignant glioma: a North American Brain Tumor Consortium report
    • Chang S.M., Kuhn J.G., Rizzo J., Robins H.I., Schold Jr. S.C., Spence A.M., et al. Phase I study of paclitaxel in patients with recurrent malignant glioma: a North American Brain Tumor Consortium report. J Clin Oncol 16 (1998) 2188-2194
    • (1998) J Clin Oncol , vol.16 , pp. 2188-2194
    • Chang, S.M.1    Kuhn, J.G.2    Rizzo, J.3    Robins, H.I.4    Schold Jr., S.C.5    Spence, A.M.6
  • 78
    • 0031924558 scopus 로고    scopus 로고
    • Phenytoin alters the disposition of topotecan and N-desmethyl topotecan in a patient with medulloblastoma
    • Zamboni W.C., Gajjar A.J., Heideman R.L., Beijnen J.H., Rosing H., Houghton P.J., et al. Phenytoin alters the disposition of topotecan and N-desmethyl topotecan in a patient with medulloblastoma. Clin Cancer Res 4 (1998) 783-789
    • (1998) Clin Cancer Res , vol.4 , pp. 783-789
    • Zamboni, W.C.1    Gajjar, A.J.2    Heideman, R.L.3    Beijnen, J.H.4    Rosing, H.5    Houghton, P.J.6
  • 79
    • 0034702552 scopus 로고    scopus 로고
    • Adverse effect of anticonvulsants on efficacy of chemotherapy for acute lymphoblastic leukaemia
    • Relling M.V., Pui C.H., Sandlund J.T., Rivera G.K., Hancock M.L., Boyett J.M., et al. Adverse effect of anticonvulsants on efficacy of chemotherapy for acute lymphoblastic leukaemia. Lancet 356 (2000) 285-290
    • (2000) Lancet , vol.356 , pp. 285-290
    • Relling, M.V.1    Pui, C.H.2    Sandlund, J.T.3    Rivera, G.K.4    Hancock, M.L.5    Boyett, J.M.6
  • 81
    • 0035810147 scopus 로고    scopus 로고
    • Efficacy and safety of a specific inhibitor of the BCR-ABL tyrosine kinase in chronic myeloid leukemia
    • Druker B.J., Talpaz M., Resta D.J., Peng B., Buchdunger E., Ford J.M., et al. Efficacy and safety of a specific inhibitor of the BCR-ABL tyrosine kinase in chronic myeloid leukemia. N Engl J Med 344 (2001) 1031-1037
    • (2001) N Engl J Med , vol.344 , pp. 1031-1037
    • Druker, B.J.1    Talpaz, M.2    Resta, D.J.3    Peng, B.4    Buchdunger, E.5    Ford, J.M.6
  • 82
    • 0344519717 scopus 로고    scopus 로고
    • Induction of cytochrome P450 3A by paclitaxel in mice: pivotal role of the nuclear xenobiotic receptor, pregnane X receptor
    • Nallani S.C., Goodwin B., Maglich J.M., Buckley D.J., Buckley A.R., and Desai P.B. Induction of cytochrome P450 3A by paclitaxel in mice: pivotal role of the nuclear xenobiotic receptor, pregnane X receptor. Drug Metab Dispos 31 (2003) 681-684
    • (2003) Drug Metab Dispos , vol.31 , pp. 681-684
    • Nallani, S.C.1    Goodwin, B.2    Maglich, J.M.3    Buckley, D.J.4    Buckley, A.R.5    Desai, P.B.6
  • 85
    • 4344581000 scopus 로고    scopus 로고
    • Differences in the induction of cytochrome P450 3A4 by taxane anticancer drugs, docetaxel and paclitaxel, assessed employing primary human hepatocytes
    • Nallani S.C., Goodwin B., Buckley A.R., Buckley D.J., and Desai P.B. Differences in the induction of cytochrome P450 3A4 by taxane anticancer drugs, docetaxel and paclitaxel, assessed employing primary human hepatocytes. Cancer Chemother Pharmacol 54 (2004) 219-229
    • (2004) Cancer Chemother Pharmacol , vol.54 , pp. 219-229
    • Nallani, S.C.1    Goodwin, B.2    Buckley, A.R.3    Buckley, D.J.4    Desai, P.B.5
  • 86
    • 24344454303 scopus 로고    scopus 로고
    • Activation of the steroid and xenobiotic receptor (human pregnane X receptor) by nontaxane microtubule-stabilizing agents
    • Mani S., Huang H., Sundarababu S., Liu W., Kalpana G., Smith A.B., et al. Activation of the steroid and xenobiotic receptor (human pregnane X receptor) by nontaxane microtubule-stabilizing agents. Clin Cancer Res 11 (2005) 6359-6369
    • (2005) Clin Cancer Res , vol.11 , pp. 6359-6369
    • Mani, S.1    Huang, H.2    Sundarababu, S.3    Liu, W.4    Kalpana, G.5    Smith, A.B.6
  • 87
    • 0031031421 scopus 로고    scopus 로고
    • Variable contribution of cytochromes P450 2D6, 2C9 and 3A4 to the 4-hydroxylation of tamoxifen by human liver microsomes
    • Crewe H.K., Ellis S.W., Lennard M.S., and Tucker G.T. Variable contribution of cytochromes P450 2D6, 2C9 and 3A4 to the 4-hydroxylation of tamoxifen by human liver microsomes. Biochem Pharmacol 53 (1997) 171-178
    • (1997) Biochem Pharmacol , vol.53 , pp. 171-178
    • Crewe, H.K.1    Ellis, S.W.2    Lennard, M.S.3    Tucker, G.T.4
  • 88
    • 0036239630 scopus 로고    scopus 로고
    • Induction of cytochrome P450 3A4 in primary human hepatocytes and activation of the human pregnane X receptor by tamoxifen and 4-hydroxytamoxifen
    • Desai P.B., Nallani S.C., Sane R.S., Moore L.B., Goodwin B.J., Buckley D.J., et al. Induction of cytochrome P450 3A4 in primary human hepatocytes and activation of the human pregnane X receptor by tamoxifen and 4-hydroxytamoxifen. Drug Metab Dispos 30 (2002) 608-612
    • (2002) Drug Metab Dispos , vol.30 , pp. 608-612
    • Desai, P.B.1    Nallani, S.C.2    Sane, R.S.3    Moore, L.B.4    Goodwin, B.J.5    Buckley, D.J.6
  • 89
    • 0035800525 scopus 로고    scopus 로고
    • Pharmacokinetics of anastrozole and tamoxifen alone, and in combination, during adjuvant endocrine therapy for early breast cancer in postmenopausal women: a sub-protocol of the 'Arimidex and tamoxifen alone or in combination' (ATAC) trial
    • Dowsett M., Cuzick J., Howell A., and Jackson I. Pharmacokinetics of anastrozole and tamoxifen alone, and in combination, during adjuvant endocrine therapy for early breast cancer in postmenopausal women: a sub-protocol of the 'Arimidex and tamoxifen alone or in combination' (ATAC) trial. Br J Cancer 85 (2001) 317-324
    • (2001) Br J Cancer , vol.85 , pp. 317-324
    • Dowsett, M.1    Cuzick, J.2    Howell, A.3    Jackson, I.4
  • 90
    • 0027369366 scopus 로고
    • Differential activation of cyclophosphamide and ifosphamide by cytochromes P-450 2B and 3A in human liver microsomes
    • Chang T.K., Weber G.F., Crespi C.L., and Waxman D.J. Differential activation of cyclophosphamide and ifosphamide by cytochromes P-450 2B and 3A in human liver microsomes. Cancer Res 53 (1993) 5629-5637
    • (1993) Cancer Res , vol.53 , pp. 5629-5637
    • Chang, T.K.1    Weber, G.F.2    Crespi, C.L.3    Waxman, D.J.4
  • 91
    • 0030951908 scopus 로고    scopus 로고
    • Enhanced cyclophosphamide and ifosfamide activation in primary human hepatocyte cultures: response to cytochrome P-450 inducers and autoinduction by oxazaphosphorines
    • Chang T.K., Yu L., Maurel P., and Waxman D.J. Enhanced cyclophosphamide and ifosfamide activation in primary human hepatocyte cultures: response to cytochrome P-450 inducers and autoinduction by oxazaphosphorines. Cancer Res 57 (1997) 1946-1954
    • (1997) Cancer Res , vol.57 , pp. 1946-1954
    • Chang, T.K.1    Yu, L.2    Maurel, P.3    Waxman, D.J.4
  • 92
    • 0035987892 scopus 로고    scopus 로고
    • The effect of cyclophosphamide with and without dexamethasone on cytochrome P450 3A4 and 2B6 in human hepatocytes
    • Lindley C., Hamilton G., McCune J.S., Faucette S., Shord S.S., Hawke R.L., et al. The effect of cyclophosphamide with and without dexamethasone on cytochrome P450 3A4 and 2B6 in human hepatocytes. Drug Metab Dispos 30 (2002) 814-822
    • (2002) Drug Metab Dispos , vol.30 , pp. 814-822
    • Lindley, C.1    Hamilton, G.2    McCune, J.S.3    Faucette, S.4    Shord, S.S.5    Hawke, R.L.6
  • 93
    • 34248517071 scopus 로고    scopus 로고
    • Mensah-Osman E. Ecteinascidin-743 is a potent inhibitor of P450 3A4 enzyme and accumulates cytoplasmic PXR to inhibit transcription of P450 3A4 and MDR1: Implications for the enhancement of cytotoxicity to chemotherapeutic agents in osteosarcoma. 2005 ASCO Annual Meeting; 2005.
  • 94
    • 0038380364 scopus 로고    scopus 로고
    • Overcoming multidrug drug resistance in P-glycoprotein/MDR1-overexpressing cell lines by ecteinascidin 743
    • Kanzaki A., Takebayashi Y., Ren X.Q., Miyashita H., Mori S., Akiyama S., et al. Overcoming multidrug drug resistance in P-glycoprotein/MDR1-overexpressing cell lines by ecteinascidin 743. Mol Cancer Ther 1 (2002) 1327-1334
    • (2002) Mol Cancer Ther , vol.1 , pp. 1327-1334
    • Kanzaki, A.1    Takebayashi, Y.2    Ren, X.Q.3    Miyashita, H.4    Mori, S.5    Akiyama, S.6
  • 95
    • 4444264038 scopus 로고    scopus 로고
    • PXR (NR1I2): splice variants in human tissues, including brain, and identification of neurosteroids and nicotine as PXR activators
    • Lamba V., Yasuda K., Lamba J.K., Assem M., Davila J., Strom S., et al. PXR (NR1I2): splice variants in human tissues, including brain, and identification of neurosteroids and nicotine as PXR activators. Toxicol Appl Pharmacol 199 (2004) 251-265
    • (2004) Toxicol Appl Pharmacol , vol.199 , pp. 251-265
    • Lamba, V.1    Yasuda, K.2    Lamba, J.K.3    Assem, M.4    Davila, J.5    Strom, S.6
  • 96
    • 0000631990 scopus 로고    scopus 로고
    • Total isothiocyanate contents in cooked vegetables frequently consumed in singapore
    • Jiao D.Y.M., Hankin J.H., Low S.H., and Chung F.L. Total isothiocyanate contents in cooked vegetables frequently consumed in singapore. J Agric Food Chem 46 (1998) 1055-1058
    • (1998) J Agric Food Chem , vol.46 , pp. 1055-1058
    • Jiao, D.Y.M.1    Hankin, J.H.2    Low, S.H.3    Chung, F.L.4
  • 97
    • 33845904129 scopus 로고    scopus 로고
    • The dietary isothiocyanate, sulforaphane is an antagonist of the human steroid and xenobiotic nuclear receptor (SXR)
    • Zhou C., Poulton E.J., Grun F., Bammler T.K., Blumberg B., Thummel K.E., et al. The dietary isothiocyanate, sulforaphane is an antagonist of the human steroid and xenobiotic nuclear receptor (SXR). Mol Pharmacol (2006)
    • (2006) Mol Pharmacol
    • Zhou, C.1    Poulton, E.J.2    Grun, F.3    Bammler, T.K.4    Blumberg, B.5    Thummel, K.E.6
  • 98
    • 0037031809 scopus 로고    scopus 로고
    • Putative role of the orphan nuclear receptor SXR (steroid and xenobiotic receptor) in the mechanism of CYP3A4 inhibition by xenobiotics
    • Takeshita A., Taguchi M., Koibuchi N., and Ozawa Y. Putative role of the orphan nuclear receptor SXR (steroid and xenobiotic receptor) in the mechanism of CYP3A4 inhibition by xenobiotics. J Biol Chem 277 (2002) 32453-32458
    • (2002) J Biol Chem , vol.277 , pp. 32453-32458
    • Takeshita, A.1    Taguchi, M.2    Koibuchi, N.3    Ozawa, Y.4
  • 99
    • 33846230463 scopus 로고    scopus 로고
    • Inhibition of drug metabolism by blocking the activation of nuclear receptors by ketoconazole
    • Huang H., Wang H., Sinz M., Zoeckler M., Staudinger J., Redinbo M.R., et al. Inhibition of drug metabolism by blocking the activation of nuclear receptors by ketoconazole. Oncogene 26 (2007) 258-268
    • (2007) Oncogene , vol.26 , pp. 258-268
    • Huang, H.1    Wang, H.2    Sinz, M.3    Zoeckler, M.4    Staudinger, J.5    Redinbo, M.R.6
  • 100
    • 0020554589 scopus 로고
    • Ketoconazole binds to glucocorticoid receptors and exhibits glucocorticoid antagonist activity in cultured cells
    • Loose D.S., Stover E.P., and Feldman D. Ketoconazole binds to glucocorticoid receptors and exhibits glucocorticoid antagonist activity in cultured cells. J Clin Invest 72 (1983) 404-408
    • (1983) J Clin Invest , vol.72 , pp. 404-408
    • Loose, D.S.1    Stover, E.P.2    Feldman, D.3
  • 101
    • 33745253791 scopus 로고    scopus 로고
    • Ketoconazole and miconazole are antagonists of the human glucocorticoid receptor: consequences on the expression and function of the constitutive androstane receptor and the pregnane X receptor
    • Duret C., Daujat-Chavanieu M., Pascussi J.M., Pichard-Garcia L., Balaguer P., Fabre J.M., et al. Ketoconazole and miconazole are antagonists of the human glucocorticoid receptor: consequences on the expression and function of the constitutive androstane receptor and the pregnane X receptor. Mol Pharmacol 70 (2006) 329-339
    • (2006) Mol Pharmacol , vol.70 , pp. 329-339
    • Duret, C.1    Daujat-Chavanieu, M.2    Pascussi, J.M.3    Pichard-Garcia, L.4    Balaguer, P.5    Fabre, J.M.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.