메뉴 건너뛰기




Volumn 51, Issue 8, 2005, Pages 1374-1381

Contribution of CYP3A5 to the in vitro hepatic clearance of tacrolimus

Author keywords

[No Author keywords available]

Indexed keywords

13 O NORTACROLIMUS; COMPLEMENTARY DNA; CYTOCHROME P450 3A; CYTOCHROME P450 3A4; CYTOCHROME P450 3A5; CYTOCHROME P450 3A7; DRUG METABOLITE; RECOMBINANT ENZYME; TACROLIMUS; UNCLASSIFIED DRUG;

EID: 23044476217     PISSN: 00099147     EISSN: None     Source Type: Journal    
DOI: 10.1373/clinchem.2005.050047     Document Type: Article
Times cited : (195)

References (49)
  • 1
    • 0023639234 scopus 로고
    • Discovery of FK-506, a novel immunosuppressant isolated from Streptomyces tsukubaensis
    • Goto T, Kino T, Hatanaka H, Nishiyama M, Okuhara M, Kohsaka M, et al. Discovery of FK-506, a novel immunosuppressant isolated from Streptomyces tsukubaensis. Transplant Proc 1987;19:4-8.
    • (1987) Transplant Proc , vol.19 , pp. 4-8
    • Goto, T.1    Kino, T.2    Hatanaka, H.3    Nishiyama, M.4    Okuhara, M.5    Kohsaka, M.6
  • 2
    • 0036380025 scopus 로고    scopus 로고
    • Mechanisms of clinically relevant drug interactions associated with tacrolimus
    • Christians U, Jacobsen W, Benet LZ, Lampen A. Mechanisms of clinically relevant drug interactions associated with tacrolimus. Clin Pharmacokinet 2002;41:813-51.
    • (2002) Clin Pharmacokinet , vol.41 , pp. 813-851
    • Christians, U.1    Jacobsen, W.2    Benet, L.Z.3    Lampen, A.4
  • 3
    • 0032128129 scopus 로고    scopus 로고
    • Therapeutic drug monitoring of cyclosporine and tacrolimus. Update on Lake Louise Consensus Conference on cyclosporin and tacrolimus
    • Oellerich M, Armstrong VW, Schutz E, Shaw LM. Therapeutic drug monitoring of cyclosporine and tacrolimus. Update on Lake Louise Consensus Conference on cyclosporin and tacrolimus. Clin Biochem 1998;31:309-16.
    • (1998) Clin Biochem , vol.31 , pp. 309-316
    • Oellerich, M.1    Armstrong, V.W.2    Schutz, E.3    Shaw, L.M.4
  • 5
    • 0026040922 scopus 로고
    • Isolation and mass spectrometric identification of five metabolites of FK-506, a novel macrolide immunosuppressive agent, from human plasma
    • Lhoest G, Wallemacq P, Verbeeck R. Isolation and mass spectrometric identification of five metabolites of FK-506, a novel macrolide immunosuppressive agent, from human plasma. Pharm Acta Helv 1991;66:302-6.
    • (1991) Pharm Acta Helv , vol.66 , pp. 302-306
    • Lhoest, G.1    Wallemacq, P.2    Verbeeck, R.3
  • 6
    • 0026662551 scopus 로고
    • Cytochrome P-450 3A enzymes are responsible for biotransformation of FK506 and rapamycin in man and rat
    • Sattler M, Guengerich FP, Yun CH, Christians U, Sewing KF. Cytochrome P-450 3A enzymes are responsible for biotransformation of FK506 and rapamycin in man and rat. Drug Metab Dispos 1992;20:753-61.
    • (1992) Drug Metab Dispos , vol.20 , pp. 753-761
    • Sattler, M.1    Guengerich, F.P.2    Yun, C.H.3    Christians, U.4    Sewing, K.F.5
  • 7
    • 0026681640 scopus 로고
    • In vitro metabolism of FK-506 in rat, rabbit, and human liver microsomes: Identification of a major metabolite and of cytochrome P450 3A as the major enzymes responsible for its metabolism
    • Vincent SH, Karanam BV, Painter SK, Chiu SH. In vitro metabolism of FK-506 in rat, rabbit, and human liver microsomes: identification of a major metabolite and of cytochrome P450 3A as the major enzymes responsible for its metabolism. Arch Biochem Biophys 1992;294:454-60.
    • (1992) Arch Biochem Biophys , vol.294 , pp. 454-460
    • Vincent, S.H.1    Karanam, B.V.2    Painter, S.K.3    Chiu, S.H.4
  • 8
    • 0028349192 scopus 로고
    • 15-Desmethyl FK-506 and 15,31-desmethyl FK-506 from human liver microsomes: Isolation, identification (by fast atom bombardment mass spectrometry and NMR), and evaluation of in vitro immunosuppressive activity
    • Lhoest GJ, Maton N, Latinne D, Laurent A, Verbeeck RK. 15-Desmethyl FK-506 and 15,31-desmethyl FK-506 from human liver microsomes: isolation, identification (by fast atom bombardment mass spectrometry and NMR), and evaluation of in vitro immunosuppressive activity. Clin Chem 1994;40:740-4.
    • (1994) Clin Chem , vol.40 , pp. 740-744
    • Lhoest, G.J.1    Maton, N.2    Latinne, D.3    Laurent, A.4    Verbeeck, R.K.5
  • 9
    • 0028295725 scopus 로고
    • Metabolism of FK506, a potent immunosuppressive agent, by cytochrome P450 3A enzymes in rat, dog and human liver microsomes
    • Shiraga T, Matsuda H, Nagase K, Iwasaki K, Noda K, Yamazaki H, et al. Metabolism of FK506, a potent immunosuppressive agent, by cytochrome P450 3A enzymes in rat, dog and human liver microsomes. Biochem Pharmacol 1994;47:727-35.
    • (1994) Biochem Pharmacol , vol.47 , pp. 727-735
    • Shiraga, T.1    Matsuda, H.2    Nagase, K.3    Iwasaki, K.4    Noda, K.5    Yamazaki, H.6
  • 10
    • 0027994206 scopus 로고
    • FK 506 metabolism in human liver microsomes: Investigation of the involvement of cytochrome P450 isozymes other than CYP3A4
    • Karanam BV, Vincent SH, Newton DJ, Wang RW, Chiu SH. FK 506 metabolism in human liver microsomes: investigation of the involvement of cytochrome P450 isozymes other than CYP3A4. Drug Metab Dispos 1994;22:811-4.
    • (1994) Drug Metab Dispos , vol.22 , pp. 811-814
    • Karanam, B.V.1    Vincent, S.H.2    Newton, D.J.3    Wang, R.W.4    Chiu, S.H.5
  • 11
    • 0029560982 scopus 로고
    • Metabolism of the immunosuppressant tacrolimus in the small intestine: Cytochrome P450, drug interactions, and interindividual variability
    • Lampen A, Christians U, Guengerich FP, Watkins PB, Kolars JC, Bader A, et al. Metabolism of the immunosuppressant tacrolimus in the small intestine: cytochrome P450, drug interactions, and interindividual variability. Drug Metab Dispos 1995;23:1315-24.
    • (1995) Drug Metab Dispos , vol.23 , pp. 1315-1324
    • Lampen, A.1    Christians, U.2    Guengerich, F.P.3    Watkins, P.B.4    Kolars, J.C.5    Bader, A.6
  • 13
    • 0035071598 scopus 로고    scopus 로고
    • Sequence diversity in CYP3A promoters and characterization of the genetic basis of polymorphic CYP3A5 expression
    • Kuehl P, Zhang J, Lin Y, Lamba J, Assem M, Schuetz J, et al. Sequence diversity in CYP3A promoters and characterization of the genetic basis of polymorphic CYP3A5 expression. Nat Genet 2001;27:383-91.
    • (2001) Nat Genet , vol.27 , pp. 383-391
    • Kuehl, P.1    Zhang, J.2    Lin, Y.3    Lamba, J.4    Assem, M.5    Schuetz, J.6
  • 14
    • 12144286933 scopus 로고    scopus 로고
    • The effect of CYP3A5 and MDR1 (ABCB1) polymorphisms on cyclosporine and tacrolimus dose requirements and trough blood levels in stable renal transplant patients
    • Haufroid V, Mourad M, Van Kerchkove V, Wawrzyniak J, De Meyer M, Eddour DC, et al. The effect of CYP3A5 and MDR1 (ABCB1) polymorphisms on cyclosporine and tacrolimus dose requirements and trough blood levels in stable renal transplant patients. Pharmacogenetics 2004;14:147-54.
    • (2004) Pharmacogenetics , vol.14 , pp. 147-154
    • Haufroid, V.1    Mourad, M.2    Van Kerchkove, V.3    Wawrzyniak, J.4    De Meyer, M.5    Eddour, D.C.6
  • 15
    • 0037115210 scopus 로고    scopus 로고
    • Tacrolimus pharmacogenetics: Polymorphisms associated with expression of cytochrome p4503A5 and P-glycoprotein correlate with dose requirement
    • MacPhee IA, Fredericks S, Tai T, Syrris P, Carter ND, Johnston A, et al. Tacrolimus pharmacogenetics: polymorphisms associated with expression of cytochrome p4503A5 and P-glycoprotein correlate with dose requirement. Transplantation 2002;74:1486-9.
    • (2002) Transplantation , vol.74 , pp. 1486-1489
    • MacPhee, I.A.1    Fredericks, S.2    Tai, T.3    Syrris, P.4    Carter, N.D.5    Johnston, A.6
  • 16
    • 0041831261 scopus 로고    scopus 로고
    • Genetic polymorphisms of the CYP3A4, CYP3A5, and MDR-1 genes and pharmacokinetics of the calcineurin inhibitors cyclosporine and tacrolimus
    • Hesselink DA, van Schaik RH, van der Heiden IP, van Dam T, van der Werf M, Weimar W, et al. Genetic polymorphisms of the CYP3A4, CYP3A5, and MDR-1 genes and pharmacokinetics of the calcineurin inhibitors cyclosporine and tacrolimus. Clin Pharmacol Ther 2003;74:245-54.
    • (2003) Clin Pharmacol Ther , vol.74 , pp. 245-254
    • Hesselink, D.A.1    Van Schaik, R.H.2    Van Der Heiden, I.P.3    Van Dam, T.4    Van Der Werf, M.5    Weimar, W.6
  • 17
    • 0242332169 scopus 로고    scopus 로고
    • Impact of cytochrome p450 3A5 genetic polymorphism on tacrolimus closes and concentration-to-dose ratio in renal transplant recipients
    • Thervet E, Anglicheau D, King B, Schlageter MH, Cassinat B, Beaune P, et al. Impact of cytochrome p450 3A5 genetic polymorphism on tacrolimus closes and concentration-to-dose ratio in renal transplant recipients. Transplantation 2003;76:1233-5.
    • (2003) Transplantation , vol.76 , pp. 1233-1235
    • Thervet, E.1    Anglicheau, D.2    King, B.3    Schlageter, M.H.4    Cassinat, B.5    Beaune, P.6
  • 18
    • 0037693831 scopus 로고    scopus 로고
    • Tacrolimus dosing in pediatric heart transplant patients is related to CYP3A5 and MDR1 gene polymorphisms
    • Zheng H, Webber S, Zetivi A, Schuetz E, Zhang J, Bowman P, ,et al. Tacrolimus dosing in pediatric heart transplant patients is related to CYP3A5 and MDR1 gene polymorphisms. Am J Transplant 2003;3:477-83.
    • (2003) Am J Transplant , vol.3 , pp. 477-483
    • Zheng, H.1    Webber, S.2    Zetivi, A.3    Schuetz, E.4    Zhang, J.5    Bowman, P.6
  • 19
    • 9144245517 scopus 로고    scopus 로고
    • Tacrolimus dosing in adult lung transplant patients is related to cytochrome P4503A5 gene polymorphism
    • Zheng H, Zeevi A, Schuetz E, Lamba J, McCurry K, Griffith BP, et al. Tacrolimus dosing in adult lung transplant patients is related to cytochrome P4503A5 gene polymorphism. J Clin Pharmacol 2004;44:135-40.
    • (2004) J Clin Pharmacol , vol.44 , pp. 135-140
    • Zheng, H.1    Zeevi, A.2    Schuetz, E.3    Lamba, J.4    McCurry, K.5    Griffith, B.P.6
  • 21
    • 14044278166 scopus 로고    scopus 로고
    • Tacrolimus pharmacogenetics: The CYP3A5*1 allele predicts low dose-normalized tacrolimus blood concentrations in whites and South Asians
    • Macphee IA, Fredericks S, Mohamed M, Moreton M, Carter ND, Johnston A, et al. Tacrolimus pharmacogenetics: the CYP3A5*1 allele predicts low dose-normalized tacrolimus blood concentrations in whites and South Asians. Transplantation 2005;79:499-502.
    • (2005) Transplantation , vol.79 , pp. 499-502
    • Macphee, I.A.1    Fredericks, S.2    Mohamed, M.3    Moreton, M.4    Carter, N.D.5    Johnston, A.6
  • 22
    • 1642329997 scopus 로고    scopus 로고
    • A genetic test for immunosuppressant dose selection?
    • Thummel KE. A genetic test for immunosuppressant dose selection? Pharmacogenetics 2004;14:145-6.
    • (2004) Pharmacogenetics , vol.14 , pp. 145-146
    • Thummel, K.E.1
  • 23
    • 2942588886 scopus 로고    scopus 로고
    • The influence of pharmacogenetics on the time to achieve target tacrolimus concentrations after kidney transplantation
    • MacPhee IA, Fredericks S, Tai T, Syrris P, Carter ND, Johnston A, et al. The influence of pharmacogenetics on the time to achieve target tacrolimus concentrations after kidney transplantation. Am J Transplant 2004;4:914-9.
    • (2004) Am J Transplant , vol.4 , pp. 914-919
    • MacPhee, I.A.1    Fredericks, S.2    Tai, T.3    Syrris, P.4    Carter, N.D.5    Johnston, A.6
  • 24
    • 4644231469 scopus 로고    scopus 로고
    • The induction of cytochrome P450 3A5 (CYP3A5) in the human liver and intestine is mediated by the xenobiotic sensors pregnane X receptor (PXR) and constitutively activated receptor (CAR)
    • Burk O, Koch I, Raucy J, Mustert E, Eichelbaum M, Brockmoller J, et al. The induction of cytochrome P450 3A5 (CYP3A5) in the human liver and intestine is mediated by the xenobiotic sensors pregnane X receptor (PXR) and constitutively activated receptor (CAR). J Biol Chem 2004;279:38379-85.
    • (2004) J Biol Chem , vol.279 , pp. 38379-38385
    • Burk, O.1    Koch, I.2    Raucy, J.3    Mustert, E.4    Eichelbaum, M.5    Brockmoller, J.6
  • 26
    • 0030933378 scopus 로고    scopus 로고
    • Functional properties of CYP2D6 1 (wild-type) and CYP2D6 7 (His324Pro) expressed by recombinant baculovirus in insect cells
    • Evert B, Eichelbaum M, Haubruck H, Zanger UM. Functional properties of CYP2D6 1 (wild-type) and CYP2D6 7 (His324Pro) expressed by recombinant baculovirus in insect cells. Naunyn Schmiedebergs Arch Pharmacol 1997;355:309-18.
    • (1997) Naunyn Schmiedebergs Arch Pharmacol , vol.355 , pp. 309-318
    • Evert, B.1    Eichelbaum, M.2    Haubruck, H.3    Zanger, U.M.4
  • 27
    • 0033674502 scopus 로고    scopus 로고
    • Comparison between cytochrome P450 (CYP) content and relative activity approaches to scaling from cDNA-expressed CYPs to human liver microsomes: Ratios of accessory proteins as sources of discrepancies between the approaches
    • Venkatakrishnan K, von Moltke LL, Court MH, Harmatz JS, Crespi CL, Greenblatt DJ. Comparison between cytochrome P450 (CYP) content and relative activity approaches to scaling from cDNA-expressed CYPs to human liver microsomes: ratios of accessory proteins as sources of discrepancies between the approaches. Drug Metab Dispos 2000;28:1493-504.
    • (2000) Drug Metab Dispos , vol.28 , pp. 1493-1504
    • Venkatakrishnan, K.1    Von Moltke, L.L.2    Court, M.H.3    Harmatz, J.S.4    Crespi, C.L.5    Greenblatt, D.J.6
  • 28
    • 0028342648 scopus 로고
    • Utility of in vitro drug metabolism data in predicting in vivo metabolic clearance
    • Houston JB, Utility of in vitro drug metabolism data in predicting in vivo metabolic clearance. Biochem Pharmacol 1994;47:1469-79.
    • (1994) Biochem Pharmacol , vol.47 , pp. 1469-1479
    • Houston, J.B.1
  • 29
    • 0035079928 scopus 로고    scopus 로고
    • Application of the relative activity factor approach in scaling from heterologously expressed cytochromes p450 to human liver microsomes studies on amitriptyline as a model substrate
    • Venkatakrishnan K, von Moltke LL, Greenblatt DJ. Application of the relative activity factor approach in scaling from heterologously expressed cytochromes p450 to human liver microsomes studies on amitriptyline as a model substrate. J Pharmacol Exp Ther 2001;297:326-37.
    • (2001) J Pharmacol Exp Ther , vol.297 , pp. 326-337
    • Venkatakrishnan, K.1    Von Moltke, L.L.2    Greenblatt, D.J.3
  • 30
    • 0032995197 scopus 로고    scopus 로고
    • Microsomal prediction of in vivo clearance of CYP2C9 substrates in humans
    • Carlile DJ, Hakooz N, Bayliss MK, Houston JB. Microsomal prediction of in vivo clearance of CYP2C9 substrates in humans. Br J Clin Pharmacol 1999;47:625-35.
    • (1999) Br J Clin Pharmacol , vol.47 , pp. 625-635
    • Carlile, D.J.1    Hakooz, N.2    Bayliss, M.K.3    Houston, J.B.4
  • 33
    • 0032733974 scopus 로고    scopus 로고
    • Prediction of human clearance of twenty-nine drugs from hepatic microsomal intrinsic clearance data: An examination of in vitro half-life approach and nonspecific binding to microsomes
    • Obach RS. Prediction of human clearance of twenty-nine drugs from hepatic microsomal intrinsic clearance data: an examination of in vitro half-life approach and nonspecific binding to microsomes. Drug Metab Dispos 1999;27:1350-9.
    • (1999) Drug Metab Dispos , vol.27 , pp. 1350-1359
    • Obach, R.S.1
  • 34
    • 0017603437 scopus 로고
    • Hepatic clearance of drugs. I. Theoretical considerations of a "well-stirred "model and a "parallel tube" model. Influence of hepatic blood flow, plasma and blood cell binding, and the hepatocellular enzymatic activity on hepatic drug clearance
    • Pang KS, Rowland M. Hepatic clearance of drugs. I. Theoretical considerations of a "well-stirred "model and a "parallel tube" model. Influence of hepatic blood flow, plasma and blood cell binding, and the hepatocellular enzymatic activity on hepatic drug clearance. J Pharmacokinet Biopharm 1977;5:625-53.
    • (1977) J Pharmacokinet Biopharm , vol.5 , pp. 625-653
    • Pang, K.S.1    Rowland, M.2
  • 35
    • 0016566218 scopus 로고
    • Commentary: A physiological approach to hepatic drug clearance
    • Wilkinson GR, Shand DG. Commentary: a physiological approach to hepatic drug clearance. Clin Pharmacol Ther 1975;18:377-90.
    • (1975) Clin Pharmacol Ther , vol.18 , pp. 377-390
    • Wilkinson, G.R.1    Shand, D.G.2
  • 37
    • 0028912205 scopus 로고
    • Expression of cytochrome P450 3A5 in Escherichia coli: Effects of 5′ modification, purification, spectral characterization, reconstitution conditions, and catalytic activities
    • Gillam EM, Quo Z, Ueng YF, Yamazaki H, Cock I, Reilly PE, et al. Expression of cytochrome P450 3A5 in Escherichia coli: effects of 5′ modification, purification, spectral characterization, reconstitution conditions, and catalytic activities. Arch Biochem Biophys 1995;317:374-84.
    • (1995) Arch Biochem Biophys , vol.317 , pp. 374-384
    • Gillam, E.M.1    Quo, Z.2    Ueng, Y.F.3    Yamazaki, H.4    Cock, I.5    Reilly, P.E.6
  • 39
  • 40
    • 0037025341 scopus 로고    scopus 로고
    • Molecular mechanisms of polymorphic CYP3A7 expression in adult human liver and intestine
    • Burk O, Tegude H, Koch I, Mustert E, Wolbold R, Glaeser H, et al. Molecular mechanisms of polymorphic CYP3A7 expression in adult human liver and intestine. J Biol Chem 2002;277: 24280-8.
    • (2002) J Biol Chem , vol.277 , pp. 24280-24288
    • Burk, O.1    Tegude, H.2    Koch, I.3    Mustert, E.4    Wolbold, R.5    Glaeser, H.6
  • 41
    • 4644263308 scopus 로고    scopus 로고
    • CYP3A5 Contributes significantly to CYP3A-mediated drug oxidations in liver microsomes from Japanese s
    • Yamaori S, Yamazaki H, Iwano S, Kiyotani K, Matsumura K, Honda G, et al. CYP3A5 Contributes significantly to CYP3A-mediated drug oxidations in liver microsomes from Japanese s. Drug Metab Pharmacokinet 2004;19:120-9.
    • (2004) Drug Metab Pharmacokinet , vol.19 , pp. 120-129
    • Yamaori, S.1    Yamazaki, H.2    Iwano, S.3    Kiyotani, K.4    Matsumura, K.5    Honda, G.6
  • 42
    • 0036893593 scopus 로고    scopus 로고
    • Evaluation of cytochrome P450 probe substrates commonly used by the pharmaceutical industry to study in vitro drug interactions
    • Yuan R, Madani S, Wei XX, Reynolds K, Huang SM. Evaluation of cytochrome P450 probe substrates commonly used by the pharmaceutical industry to study in vitro drug interactions. Drug Metab - Dispos 2002;30:1311-9.
    • (2002) Drug Metab - Dispos , vol.30 , pp. 1311-1319
    • Yuan, R.1    Madani, S.2    Wei, X.X.3    Reynolds, K.4    Huang, S.M.5
  • 44
    • 0036707616 scopus 로고    scopus 로고
    • Differential oxidation of mifepristone by cytochromes P450 3A4 and 3A5: Selective inactivation of P450 3A4
    • Khan KK, He YQ, Correia MA, Halpert JR. Differential oxidation of mifepristone by cytochromes P450 3A4 and 3A5: selective inactivation of P450 3A4. Drug Metab Dispos 2002;30:985-90.
    • (2002) Drug Metab Dispos , vol.30 , pp. 985-990
    • Khan, K.K.1    He, Y.Q.2    Correia, M.A.3    Halpert, J.R.4
  • 45
    • 7044272257 scopus 로고    scopus 로고
    • Influence of CYP3A5 and MDR1 (ABCB1) polymorphisms on the pharmacokinetics of tacrolimus in renal transplant recipients
    • Tsuchiya N, Satoh S, Tada H, Li Z, Ohyama C, Sato K, et al. Influence of CYP3A5 and MDR1 (ABCB1) polymorphisms on the pharmacokinetics of tacrolimus in renal transplant recipients. Transplantation 2004;78:1182-7.
    • (2004) Transplantation , vol.78 , pp. 1182-1187
    • Tsuchiya, N.1    Satoh, S.2    Tada, H.3    Li, Z.4    Ohyama, C.5    Sato, K.6
  • 46
    • 3242779991 scopus 로고    scopus 로고
    • CYP3A5*1-carrying graft liver reduces the concentration/oral dose ratio of tacrolimus in recipients of living-donor liver transplantation
    • Goto M, Masuda S, Kiuchi T, Ogura Y, Oike F, Okuda M, Tanaka K, et al. CYP3A5*1-carrying graft liver reduces the concentration/oral dose ratio of tacrolimus in recipients of living-donor liver transplantation, Pharmacogenetics 2004;14:471-8.
    • (2004) Pharmacogenetics , vol.14 , pp. 471-478
    • Goto, M.1    Masuda, S.2    Kiuchi, T.3    Ogura, Y.4    Oike, F.5    Okuda, M.6    Tanaka, K.7
  • 47
    • 0035805536 scopus 로고    scopus 로고
    • Nuclear receptor response elements mediate induction of intestinal MDR1 by rifampin
    • Geick A, Eichelbaum M, Burk O. Nuclear receptor response elements mediate induction of intestinal MDR1 by rifampin, J Biol Chem 2001;276:14581-7.
    • (2001) J Biol Chem , vol.276 , pp. 14581-14587
    • Geick, A.1    Eichelbaum, M.2    Burk, O.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.