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Volumn 7, Issue 4, 2007, Pages 447-459

Tariquidar (XR9576): A P-glycoprotein drug efflux pump inhibitor

Author keywords

MDR; Multidrug resistance; P glycoprotein; Tariquidar

Indexed keywords

ADENOSINE TRIPHOSPHATASE; ANTHRACYCLINE DERIVATIVE; ANTINEOPLASTIC AGENT; CARBOPLATIN; CYCLOSPORIN; CYTARABINE; CYTOTOXIC AGENT; DAUNORUBICIN; DEXNIGULDIPINE; DOCETAXEL; DOXORUBICIN; ETOPOSIDE; GEMTUZUMAB OZOGAMICIN; GLYCOPROTEIN P; GLYCOPROTEIN P INHIBITOR; LANIQUIDAR; MITOTANE; NAVELBINE; ONT 093; PACLITAXEL; PLACEBO; TAMOXIFEN; TARIQUIDAR; TAXANE DERIVATIVE; TRASTUZUMAB; UNCLASSIFIED DRUG; UNINDEXED DRUG; VALSPODAR; VINBLASTINE; VINCRISTINE; ZOSUQUIDAR;

EID: 34247646575     PISSN: 14737140     EISSN: 17448328     Source Type: Journal    
DOI: 10.1586/14737140.7.4.447     Document Type: Article
Times cited : (305)

References (106)
  • 1
    • 0036176510 scopus 로고    scopus 로고
    • Mechanisms of cancer drug resistance
    • Gottesman MM. Mechanisms of cancer drug resistance. Annu. Rev. Med. 53, 615-627 (2002).
    • (2002) Annu. Rev. Med , vol.53 , pp. 615-627
    • Gottesman, M.M.1
  • 2
    • 0038199888 scopus 로고    scopus 로고
    • Drug resistance in cancer: A multifactorial problem
    • 232C, 1769-1772
    • Mattern J. Drug resistance in cancer: a multifactorial problem. Anticancer Res. 23(2C), 1769-1772 (2003).
    • (2003) Anticancer Res
    • Mattern, J.1
  • 3
    • 27644575716 scopus 로고    scopus 로고
    • Drug resistance in cancer
    • Yague E, Raguz S. Drug resistance in cancer. Br. J. Cancer 93(9), 973-976 (2005).
    • (2005) Br. J. Cancer , vol.93 , Issue.9 , pp. 973-976
    • Yague, E.1    Raguz, S.2
  • 4
    • 0034917716 scopus 로고    scopus 로고
    • The human ATP-binding cassette (ABC) transporter superfamily
    • Dean M, Rzhetsky A, Allikmets R. The human ATP-binding cassette (ABC) transporter superfamily. Genome Res. 11(7), 1156-1166 (2001).
    • (2001) Genome Res , vol.11 , Issue.7 , pp. 1156-1166
    • Dean, M.1    Rzhetsky, A.2    Allikmets, R.3
  • 5
    • 33745748312 scopus 로고    scopus 로고
    • The functions and structure of ABC transporters: Implications for the design of new inhibitors of Pgp and MRP1 to control multidrug resistance (MDR)
    • Teodori E, Dei S, Martelli C, Scapecchi S, Gualtieri F. The functions and structure of ABC transporters: implications for the design of new inhibitors of Pgp and MRP1 to control multidrug resistance (MDR). Curr. Drug Targets 7(7), 893-909 (2006).
    • (2006) Curr. Drug Targets , vol.7 , Issue.7 , pp. 893-909
    • Teodori, E.1    Dei, S.2    Martelli, C.3    Scapecchi, S.4    Gualtieri, F.5
  • 6
    • 33749488939 scopus 로고    scopus 로고
    • Human multidrug resistance ABCB and ABCG transporters: Participation in a chemoimmunity defense system
    • Sarkadi B, Homolya L, Szakacs G, Varadi A. Human multidrug resistance ABCB and ABCG transporters: participation in a chemoimmunity defense system. Physiol. Rev. 86(4), 1179-1236 (2006).
    • (2006) Physiol. Rev , vol.86 , Issue.4 , pp. 1179-1236
    • Sarkadi, B.1    Homolya, L.2    Szakacs, G.3    Varadi, A.4
  • 7
    • 33645830172 scopus 로고
    • A surface glycoprotein modulating drug permeability in Chinese hamster ovary cell mutants
    • Juliano RL, Ling V. A surface glycoprotein modulating drug permeability in Chinese hamster ovary cell mutants. Biochim. Biopbys. Acta 455(1), 152-62 (1976).
    • (1976) Biochim. Biopbys. Acta , vol.455 , Issue.1 , pp. 152-162
    • Juliano, R.L.1    Ling, V.2
  • 9
    • 0030986845 scopus 로고    scopus 로고
    • Expression of drug resistance proteins in breast cancer, in relation to chemotherapy
    • Linn SC, Pinedo HM, van Ark-Otte J et al. Expression of drug resistance proteins in breast cancer, in relation to chemotherapy. Int. J. Cancer 71(5), 787-795 (1997).
    • (1997) Int. J. Cancer , vol.71 , Issue.5 , pp. 787-795
    • Linn, S.C.1    Pinedo, H.M.2    van Ark-Otte, J.3
  • 10
    • 0024460547 scopus 로고
    • Expression of a drug resistance gene in human neuroblastoma cell lines: Modulation by retinoic acid-induced differentiation
    • Bates SE, Mickley LA, Chen YN et al. Expression of a drug resistance gene in human neuroblastoma cell lines: modulation by retinoic acid-induced differentiation. Mol. Cell. Biol. 9(10), 4337-4344 (1989).
    • (1989) Mol. Cell. Biol , vol.9 , Issue.10 , pp. 4337-4344
    • Bates, S.E.1    Mickley, L.A.2    Chen, Y.N.3
  • 11
  • 13
    • 0034092081 scopus 로고    scopus 로고
    • Incidence of P-glycoprotein overexpression and multidrug resistance (MDR) reversal in adult soft tissue sarcoma
    • Coley HM, Verrill MW, Gregson SE, Odell DE, Fisher C, Judson IR. Incidence of P-glycoprotein overexpression and multidrug resistance (MDR) reversal in adult soft tissue sarcoma. Eur. J. Cancer 36(7), 881-888 (2000).
    • (2000) Eur. J. Cancer , vol.36 , Issue.7 , pp. 881-888
    • Coley, H.M.1    Verrill, M.W.2    Gregson, S.E.3    Odell, D.E.4    Fisher, C.5    Judson, I.R.6
  • 14
    • 13444252391 scopus 로고    scopus 로고
    • MDR1 and MRP1 gene expression are independent predictors for treatment outcome in adult acute myeloid leukaemia
    • Schaich M, Soucek S, Thiede C, Ehninger G, Illmer T. MDR1 and MRP1 gene expression are independent predictors for treatment outcome in adult acute myeloid leukaemia. Br. J. Haematol. 128(3), 324-332 (2005).
    • (2005) Br. J. Haematol , vol.128 , Issue.3 , pp. 324-332
    • Schaich, M.1    Soucek, S.2    Thiede, C.3    Ehninger, G.4    Illmer, T.5
  • 15
    • 6444245006 scopus 로고    scopus 로고
    • CD56 and PGP expression in acute myeloid leukemia: Impact on clinical outcome
    • Raspadori D, Damiani D, Michieli M et al. CD56 and PGP expression in acute myeloid leukemia: impact on clinical outcome. Haematologica 87(11), 1135-1140 (2002).
    • (2002) Haematologica , vol.87 , Issue.11 , pp. 1135-1140
    • Raspadori, D.1    Damiani, D.2    Michieli, M.3
  • 16
    • 0031731764 scopus 로고    scopus 로고
    • P-glycoprotein expression and prognostic value in acute myeloid leukemia
    • Senent L, Jarque I, Martin G et al. P-glycoprotein expression and prognostic value in acute myeloid leukemia. Haematologica 83(9), 783-787 (1998).
    • (1998) Haematologica , vol.83 , Issue.9 , pp. 783-787
    • Senent, L.1    Jarque, I.2    Martin, G.3
  • 17
    • 0031052883 scopus 로고    scopus 로고
    • Multidrug resistance gene expression in acute myeloid leukemia: Major prognosis significance for in vivo drug resistance to induction treatment
    • Hunault M, Zhou D, Delmer A et al. Multidrug resistance gene expression in acute myeloid leukemia: major prognosis significance for in vivo drug resistance to induction treatment. Ann. Hematol. 74(2), 65-71 (1997).
    • (1997) Ann. Hematol , vol.74 , Issue.2 , pp. 65-71
    • Hunault, M.1    Zhou, D.2    Delmer, A.3
  • 18
    • 0030729284 scopus 로고    scopus 로고
    • MDR 1 expression is an independent prognostic factor for response and survival in de novo acute myeloid leukaemia
    • van den Heuvel-Eibrink MM, van der Holt B, te Bockhorst PA et al. MDR 1 expression is an independent prognostic factor for response and survival in de novo acute myeloid leukaemia. Br. J. Haematol. 99(1), 76-83 (1997).
    • (1997) Br. J. Haematol , vol.99 , Issue.1 , pp. 76-83
    • van den Heuvel-Eibrink, M.M.1    van der Holt, B.2    te Bockhorst, P.A.3
  • 19
    • 0035383769 scopus 로고    scopus 로고
    • MDR1 gene-related clonal selection and P-glycoprotein function and expression in relapsed or refractory acute myeloid leukemia
    • van den Heuvel-Eibrink MM, Wiemer EA, de Boevere MJ et al. MDR1 gene-related clonal selection and P-glycoprotein function and expression in relapsed or refractory acute myeloid leukemia. Blood 97(11), 3605-3611 (2001).
    • (2001) Blood , vol.97 , Issue.11 , pp. 3605-3611
    • van den Heuvel-Eibrink, M.M.1    Wiemer, E.A.2    de Boevere, M.J.3
  • 20
    • 0028244591 scopus 로고
    • P-glycoprotein expression on acute myeloid leukaemia blast cells at diagnosis predicts response to chemotherapy and survival
    • Wood P, Burgess R, MacGregor A, Yin JA. P-glycoprotein expression on acute myeloid leukaemia blast cells at diagnosis predicts response to chemotherapy and survival. Br J. Haematol., 87(3), 509-514 (1994).
    • (1994) Br J. Haematol , vol.87 , Issue.3 , pp. 509-514
    • Wood, P.1    Burgess, R.2    MacGregor, A.3    Yin, J.A.4
  • 21
    • 0035992274 scopus 로고    scopus 로고
    • P-glycoprotein in acute myeloid leukaemia: Therapeutic implications of its association with both a multidrug-resistant and an apoptosis-resistant phenotype
    • Pallis M, Turzanski J, Higashi Y, Russell N. P-glycoprotein in acute myeloid leukaemia: therapeutic implications of its association with both a multidrug-resistant and an apoptosis-resistant phenotype. Leuk. Lymphoma 43(6), 1221-1228 (2002).
    • (2002) Leuk. Lymphoma , vol.43 , Issue.6 , pp. 1221-1228
    • Pallis, M.1    Turzanski, J.2    Higashi, Y.3    Russell, N.4
  • 22
    • 0030058445 scopus 로고    scopus 로고
    • Role of multidrug resistance and its pharmacological modulation in acute myeloid leukemia
    • List AF. Role of multidrug resistance and its pharmacological modulation in acute myeloid leukemia. Leukemia 10(6), 937-942 (1996).
    • (1996) Leukemia , vol.10 , Issue.6 , pp. 937-942
    • List, A.F.1
  • 23
    • 0034009217 scopus 로고    scopus 로고
    • Novel mechanisms of drug resistance in leukemia
    • Ross DD. Novel mechanisms of drug resistance in leukemia. Leukemia 14(3), 467-473 (2000).
    • (2000) Leukemia , vol.14 , Issue.3 , pp. 467-473
    • Ross, D.D.1
  • 24
    • 0344393732 scopus 로고    scopus 로고
    • Strategies for reversing drug resistance
    • Fojo T, Bates S. Strategies for reversing drug resistance. Oncogene 22(47), 7512-7523 (2003).
    • (2003) Oncogene , vol.22 , Issue.47 , pp. 7512-7523
    • Fojo, T.1    Bates, S.2
  • 25
    • 0036355399 scopus 로고    scopus 로고
    • Reversal of multidrug resistance: Lessons from clinical oncology
    • Discussion 102, 80-85
    • Bates SF, Chen C, Robey R, Kang M, Figg WD, Fojo T. Reversal of multidrug resistance: lessons from clinical oncology. Novartis Found. Symp. 243, 83-96; Discussion 102, 80-85 (2002).
    • (2002) Novartis Found. Symp , vol.243 , pp. 83-96
    • Bates, S.F.1    Chen, C.2    Robey, R.3    Kang, M.4    Figg, W.D.5    Fojo, T.6
  • 26
    • 0025007511 scopus 로고
    • Pharmacology of drugs that alter multidrug resistance in cancer
    • Ford JM, Hait WN. Pharmacology of drugs that alter multidrug resistance in cancer. Pharmacol. Rev. 42(3), 155-199 (1990).
    • (1990) Pharmacol. Rev , vol.42 , Issue.3 , pp. 155-199
    • Ford, J.M.1    Hait, W.N.2
  • 27
    • 0345411341 scopus 로고    scopus 로고
    • P-glycoprotein and cytochrome P-450 3A inhibition: Dissociation of inhibitory potencies
    • Wandel C, Kim RB, Kajiji S, Guengerich P, Wilkinson GR, Wood AJ. P-glycoprotein and cytochrome P-450 3A inhibition: dissociation of inhibitory potencies. Cancer Res. 59(16), 3944-3948 (1999).
    • (1999) Cancer Res , vol.59 , Issue.16 , pp. 3944-3948
    • Wandel, C.1    Kim, R.B.2    Kajiji, S.3    Guengerich, P.4    Wilkinson, G.R.5    Wood, A.J.6
  • 28
    • 0345084436 scopus 로고    scopus 로고
    • The multidrug resistance modulator valspodar (PSC 833) is metabolized by human cytochrome P450 3A. Implications for drug-drug interactions and pharmacological activity of the main metabolite
    • Fischer V, Rodriguez-Gascon A, Heitz F et al. The multidrug resistance modulator valspodar (PSC 833) is metabolized by human cytochrome P450 3A. Implications for drug-drug interactions and pharmacological activity of the main metabolite. Drug Metab. Dispos. 26(8), 802-811 (1998).
    • (1998) Drug Metab. Dispos , vol.26 , Issue.8 , pp. 802-811
    • Fischer, V.1    Rodriguez-Gascon, A.2    Heitz, F.3
  • 29
    • 0030069632 scopus 로고    scopus 로고
    • Phase I study of etoposide with SDZ PSC 833 as a modulator of multidrug resistance in patients with cancer
    • Boote DJ, Dennis IF, Twentyman PR et al. Phase I study of etoposide with SDZ PSC 833 as a modulator of multidrug resistance in patients with cancer. J. Clin. Oncol. 14(2), 610-618 (1996).
    • (1996) J. Clin. Oncol , vol.14 , Issue.2 , pp. 610-618
    • Boote, D.J.1    Dennis, I.F.2    Twentyman, P.R.3
  • 30
    • 0037358040 scopus 로고    scopus 로고
    • Overcoming multidrug resistance in cancer an update on the clinical strategy of inhibiting p-glycoprotein
    • Thomas H, Coley HM. Overcoming multidrug resistance in cancer an update on the clinical strategy of inhibiting p-glycoprotein. Cancer Control 10(2), 159-165 (2003).
    • (2003) Cancer Control , vol.10 , Issue.2 , pp. 159-165
    • Thomas, H.1    Coley, H.M.2
  • 31
    • 0032881342 scopus 로고    scopus 로고
    • The molecular interaction of the high affinity reversal agent XR9576 with P-glycoprotein
    • Martin C, Berridge G, Mistry P, Higgins C, Charlton P, Callaghan R. The molecular interaction of the high affinity reversal agent XR9576 with P-glycoprotein. Br. J Pharmacol. 128(2), 403-411 (1999).
    • (1999) Br. J Pharmacol , vol.128 , Issue.2 , pp. 403-411
    • Martin, C.1    Berridge, G.2    Mistry, P.3    Higgins, C.4    Charlton, P.5    Callaghan, R.6
  • 32
    • 0033593855 scopus 로고    scopus 로고
    • Reversal of P-glycoprotein mediated multidrug resistance by novel anthranilamide derivatives
    • Roe M, Folkes A, Ashworth P et al. Reversal of P-glycoprotein mediated multidrug resistance by novel anthranilamide derivatives. Bioorg. Med. Chem. Lett. 9(4), 595-600 (1999).
    • (1999) Bioorg. Med. Chem. Lett , vol.9 , Issue.4 , pp. 595-600
    • Roe, M.1    Folkes, A.2    Ashworth, P.3
  • 33
    • 31044448979 scopus 로고    scopus 로고
    • Structute-activity relationships of a series of tariquidar analogs as multidrug resistance modulators
    • Globisch C, Pajeva IK, Wiese M. Structute-activity relationships of a series of tariquidar analogs as multidrug resistance modulators. Bioorg. Med. Chem. 14(5), 1588-1598 (2006).
    • (2006) Bioorg. Med. Chem , vol.14 , Issue.5 , pp. 1588-1598
    • Globisch, C.1    Pajeva, I.K.2    Wiese, M.3
  • 34
    • 0035863315 scopus 로고    scopus 로고
    • In vitro and in vivo reversal of P-glycoprotein-mediated multidrug resistance by a novel potent modulator, XR9576
    • Mistry P, Stewart AJ, Dangerfield W et al. In vitro and in vivo reversal of P-glycoprotein-mediated multidrug resistance by a novel potent modulator, XR9576. Cancer Res. 61(2), 749-758 (2001).
    • (2001) Cancer Res , vol.61 , Issue.2 , pp. 749-758
    • Mistry, P.1    Stewart, A.J.2    Dangerfield, W.3
  • 35
    • 1242338943 scopus 로고    scopus 로고
    • Inhibition of P-glycoprotein function by XR9576 in a solid tumour model can restore anticancer drug efficacy
    • Walker J, Martin C, Callaghan R. Inhibition of P-glycoprotein function by XR9576 in a solid tumour model can restore anticancer drug efficacy. Eur. J. Cancer 40(4), 594-605 (2004).
    • (2004) Eur. J. Cancer , vol.40 , Issue.4 , pp. 594-605
    • Walker, J.1    Martin, C.2    Callaghan, R.3
  • 36
    • 1242293677 scopus 로고    scopus 로고
    • Pheophorbide A is a specific probe for ABCG2 function and inhibition
    • Robey RW, Steadman K, Polgar O et al. Pheophorbide A is a specific probe for ABCG2 function and inhibition. Cancer Res. 64(4), 1242-1246 (2004).
    • (2004) Cancer Res , vol.64 , Issue.4 , pp. 1242-1246
    • Robey, R.W.1    Steadman, K.2    Polgar, O.3
  • 37
    • 0032960840 scopus 로고    scopus 로고
    • + cells as a surrogate marker for reversal of P-glycoprotein-mediated drug efflux by PSC 833
    • + cells as a surrogate marker for reversal of P-glycoprotein-mediated drug efflux by PSC 833. Blood 93(1), 306-314 (1999).
    • (1999) Blood , vol.93 , Issue.1 , pp. 306-314
    • Robey, R.1    Bakke, S.2    Stein, W.3
  • 39
    • 0012923995 scopus 로고    scopus 로고
    • Phase I study of the novel P-glycoprotein antagonist, XR9576, in combination with vinorelbine
    • Abstract 287
    • Abraham J, Edgerly M, Wilson R et al. Phase I study of the novel P-glycoprotein antagonist, XR9576, in combination with vinorelbine. Proc. Am. Soc. Clin. Oncol. 20, 73A (2001) (Abstract 287).
    • (2001) Proc. Am. Soc. Clin. Oncol , vol.20
    • Abraham, J.1    Edgerly, M.2    Wilson, R.3
  • 40
    • 34247561734 scopus 로고    scopus 로고
    • Pediatric Phase I trial and pharmcokinetic study of the P-glycoprotien inhibitor, tariquidar, in combination with doxorubicin, vinorelbine, or docetaxel
    • Abstract 8541
    • Fox E, Widemann BC, Chen CC et al. Pediatric Phase I trial and pharmcokinetic study of the P-glycoprotien inhibitor, tariquidar, in combination with doxorubicin, vinorelbine, or docetaxel. Proc. Am. Soc. Clin. Oncol. 22(Suppl. 14), S809 (2004) (Abstract 8541).
    • (2004) Proc. Am. Soc. Clin. Oncol , vol.22 , Issue.SUPPL. 14
    • Fox, E.1    Widemann, B.C.2    Chen, C.C.3
  • 42
    • 0037316891 scopus 로고    scopus 로고
    • 99mTc-sestamibi accumulation in normal liver and drug-resistant tumors after the administration of the glycoprotein inhibitor, XR9576
    • 99mTc-sestamibi accumulation in normal liver and drug-resistant tumors after the administration of the glycoprotein inhibitor, XR9576. Clin. Cancer Res. 9(2) 650-656 (2003).
    • (2003) Clin. Cancer Res , vol.9 , Issue.2 , pp. 650-656
    • Agrawal, M.1    Abraham, J.2    Balis, F.M.3
  • 43
    • 0038582891 scopus 로고    scopus 로고
    • XR9576 (tariquidar) a potent and specific P-glycoprotien inhibitor has minimal effects on the pharmacokinetics of paclitaxel, doxorubicin, and vinorelbine, and can be administered with full-dose chemotherapy in patients with cancer
    • Abstract 2173
    • Boniface G. Ferry D, Atsmon J et al. XR9576 (tariquidar) a potent and specific P-glycoprotien inhibitor has minimal effects on the pharmacokinetics of paclitaxel, doxorubicin, and vinorelbine, and can be administered with full-dose chemotherapy in patients with cancer. Proc. Am. Soc. Clin. Oncol. 24, 90B (2002) (Abstract 2173).
    • (2002) Proc. Am. Soc. Clin. Oncol , vol.24
    • Boniface, G.1    Ferry, D.2    Atsmon, J.3
  • 44
    • 23644452472 scopus 로고    scopus 로고
    • Phase II study of tariquidar, a selective P-glycoprotein inhibitor, in patients with chemotherapy-resistant, advanced breast carcinoma
    • Pusztal L, Wagner P, Ibrahim N et al. Phase II study of tariquidar, a selective P-glycoprotein inhibitor, in patients with chemotherapy-resistant, advanced breast carcinoma. Cancer 104(4), 682-691 (2005).
    • (2005) Cancer , vol.104 , Issue.4 , pp. 682-691
    • Pusztal, L.1    Wagner, P.2    Ibrahim, N.3
  • 45
    • 33745746815 scopus 로고    scopus 로고
    • Pharmacological strategies for overcoming multidrug resistance
    • Nobili S, Landini I, Giglioni B, Mini E. Pharmacological strategies for overcoming multidrug resistance. Curr. Drug Targets 7(7), 861-879 (2006).
    • (2006) Curr. Drug Targets , vol.7 , Issue.7 , pp. 861-879
    • Nobili, S.1    Landini, I.2    Giglioni, B.3    Mini, E.4
  • 46
    • 0034006531 scopus 로고    scopus 로고
    • The orally administered P-glycoprotein inhibitor R101933 does not alter the plasma pharmacokinetics of docetaxel
    • van Zuylen L, Sparreboom A, van der Gaast A et al. The orally administered P-glycoprotein inhibitor R101933 does not alter the plasma pharmacokinetics of docetaxel. Clin. Cancer Res. 6(4), 1365-1371 (2000).
    • (2000) Clin. Cancer Res , vol.6 , Issue.4 , pp. 1365-1371
    • van Zuylen, L.1    Sparreboom, A.2    van der Gaast, A.3
  • 48
    • 11244321887 scopus 로고    scopus 로고
    • Oral bioavailability of docetaxel in combination with OC144-093 (ONT-093)
    • Kuppens IE, Bosch TM, van Maanen MJ et al. Oral bioavailability of docetaxel in combination with OC144-093 (ONT-093). Cancer Chemother. Pharmacol. 55(1), 72-78 (2005).
    • (2005) Cancer Chemother. Pharmacol , vol.55 , Issue.1 , pp. 72-78
    • Kuppens, I.E.1    Bosch, T.M.2    van Maanen, M.J.3
  • 49
    • 0036829187 scopus 로고    scopus 로고
    • Low systemic exposure of oral docetaxel in mice resulting from extensive first-pass metabolism is boosted by ritonavir
    • Bardelmeijer HA, Ouwehand M, Buckle T et al. Low systemic exposure of oral docetaxel in mice resulting from extensive first-pass metabolism is boosted by ritonavir. Cancer Res. 62(21), 6158-6164 (2002).
    • (2002) Cancer Res , vol.62 , Issue.21 , pp. 6158-6164
    • Bardelmeijer, H.A.1    Ouwehand, M.2    Buckle, T.3
  • 50
    • 2542479863 scopus 로고    scopus 로고
    • A Phase I trial of a potent P-glycoprotein inhibitor, zosuquidar trihydrochloride (LY335979), administered intravenously in combination with doxorubicin in patients with advanced malignancy
    • Sandler A, Gordon M, De Alwis DP et al. A Phase I trial of a potent P-glycoprotein inhibitor, zosuquidar trihydrochloride (LY335979), administered intravenously in combination with doxorubicin in patients with advanced malignancy. Clin. Cancer Res. 10(10), 3265-3272 (2004).
    • (2004) Clin. Cancer Res , vol.10 , Issue.10 , pp. 3265-3272
    • Sandler, A.1    Gordon, M.2    De Alwis, D.P.3
  • 51
    • 0035883604 scopus 로고    scopus 로고
    • A Phase I study of infusional vinblastine in combination with the P-glycoprotein antagonist PSC 833 (valspodar)
    • Bates S, Kang M, Meadows B et al. A Phase I study of infusional vinblastine in combination with the P-glycoprotein antagonist PSC 833 (valspodar). Cancer 92(6), 1577-1590 (2001).
    • (2001) Cancer , vol.92 , Issue.6 , pp. 1577-1590
    • Bates, S.1    Kang, M.2    Meadows, B.3
  • 52
    • 0035001004 scopus 로고    scopus 로고
    • Combined action of PSC 833 (Valspodar), a novel MDR reversing agent, with mitoxantrone, etoposide and cytarabine in poor-prognosis acute myeloid leukemia
    • Visani G, Milligan D, Leoni F et al. Combined action of PSC 833 (Valspodar), a novel MDR reversing agent, with mitoxantrone, etoposide and cytarabine in poor-prognosis acute myeloid leukemia. Leukemia 15(5), 764-771 (2001).
    • (2001) Leukemia , vol.15 , Issue.5 , pp. 764-771
    • Visani, G.1    Milligan, D.2    Leoni, F.3
  • 53
    • 28444497756 scopus 로고    scopus 로고
    • A Phase I trial of liposomal doxorubicin, paclitaxel and valspodar (PSC-833), an inhibitor of multidrug resistance
    • Advani R, Lum BL, Fisher GA et al. A Phase I trial of liposomal doxorubicin, paclitaxel and valspodar (PSC-833), an inhibitor of multidrug resistance. Ann. Oncol. 16(12), 1968-1973 (2005).
    • (2005) Ann. Oncol , vol.16 , Issue.12 , pp. 1968-1973
    • Advani, R.1    Lum, B.L.2    Fisher, G.A.3
  • 54
    • 23044500423 scopus 로고    scopus 로고
    • Phase I study of pegylated liposomal doxorubicin and the multidrug-resistance modulator, valspodar
    • Fracasso PM, Blum KA, Ma MK et al. Phase I study of pegylated liposomal doxorubicin and the multidrug-resistance modulator, valspodar. Br. J. Cancer 93(1), 46-53 (2005).
    • (2005) Br. J. Cancer , vol.93 , Issue.1 , pp. 46-53
    • Fracasso, P.M.1    Blum, K.A.2    Ma, M.K.3
  • 55
    • 30944456274 scopus 로고    scopus 로고
    • Tamoxifen paradoxically decreases paclitaxel deposition into cerebrospinal fluid of brain tumor patients
    • Chen J, Balmaceda C, Bruce JN et al. Tamoxifen paradoxically decreases paclitaxel deposition into cerebrospinal fluid of brain tumor patients. J. Neurooncol. 76(1), 85-92 (2006).
    • (2006) J. Neurooncol , vol.76 , Issue.1 , pp. 85-92
    • Chen, J.1    Balmaceda, C.2    Bruce, J.N.3
  • 56
    • 0031581672 scopus 로고    scopus 로고
    • Phase I and pharmacokinetic study of the P-glycoprotein modulator dexniguldipine-HCL
    • Nuessler V, Scheulen ME, Oberneder R et al. Phase I and pharmacokinetic study of the P-glycoprotein modulator dexniguldipine-HCL. Eur. J. Med. Res. 2(2), 55-61 (1997).
    • (1997) Eur. J. Med. Res , vol.2 , Issue.2 , pp. 55-61
    • Nuessler, V.1    Scheulen, M.E.2    Oberneder, R.3
  • 57
    • 0036895024 scopus 로고    scopus 로고
    • A Phase I trial of a potent P-glycoprotein inhibitor, Zosuquidar.3HCl trihydrochloride (LY335979), administered orally in combination with doxorubicin in patients with advanced malignancies
    • Rubin EH, de Alwis DP, Pouliquen I et al. A Phase I trial of a potent P-glycoprotein inhibitor, Zosuquidar.3HCl trihydrochloride (LY335979), administered orally in combination with doxorubicin in patients with advanced malignancies. Clin. Cancer Res. 8(12), 3710-3717 (2002).
    • (2002) Clin. Cancer Res , vol.8 , Issue.12 , pp. 3710-3717
    • Rubin, E.H.1    de Alwis, D.P.2    Pouliquen, I.3
  • 58
    • 21244504196 scopus 로고    scopus 로고
    • Phase I study of the multidrug resistance inhibitor zosuquidar administered in combination with vinorelbine in patients with advanced solid tumours
    • Le LH, Moore MJ, Siu LL et al. Phase I study of the multidrug resistance inhibitor zosuquidar administered in combination with vinorelbine in patients with advanced solid tumours. Cancer Chemother. Pharmacol. 56(2), 154-160 (2005).
    • (2005) Cancer Chemother. Pharmacol , vol.56 , Issue.2 , pp. 154-160
    • LH, L.1    Moore, M.J.2    Siu, L.L.3
  • 59
    • 3242781758 scopus 로고    scopus 로고
    • Clinical effects and P-glycoprotein inhibition in patients with acute myeloid leukemia treated with zosuquidar trihydrochloride, daunorubicin, and cytarabine
    • Gerrand G, Payne E, Baker RJ et al. Clinical effects and P-glycoprotein inhibition in patients with acute myeloid leukemia treated with zosuquidar trihydrochloride, daunorubicin, and cytarabine. Haematologica 89, 782-790 (2004).
    • (2004) Haematologica , vol.89 , pp. 782-790
    • Gerrand, G.1    Payne, E.2    Baker, R.J.3
  • 60
    • 1842457644 scopus 로고    scopus 로고
    • Mitoxantrone, etoposide, and cytarabine with or without valspodar in patients with relapsed or refractory acute myeloid leukemia and high-risk myelodysplastic syndrome: A Phase III trial (E2995)
    • Greenberg PL, Lee SJ, Advani R et al. Mitoxantrone, etoposide, and cytarabine with or without valspodar in patients with relapsed or refractory acute myeloid leukemia and high-risk myelodysplastic syndrome: a Phase III trial (E2995). J. Clin. Oncol. 22(6), 1078-1086 (2004).
    • (2004) J. Clin. Oncol , vol.22 , Issue.6 , pp. 1078-1086
    • Greenberg, P.L.1    Lee, S.J.2    Advani, R.3
  • 61
    • 0035253714 scopus 로고    scopus 로고
    • Phase I study of infusional paclitaxel in combination with the P-glycoprotein antagonist PSC 833
    • Chico I, Kang MH, Bergan R et al. Phase I study of infusional paclitaxel in combination with the P-glycoprotein antagonist PSC 833. J. Clin. Oncol. 19(3), 832-842 (2001).
    • (2001) J. Clin. Oncol , vol.19 , Issue.3 , pp. 832-842
    • Chico, I.1    Kang, M.H.2    Bergan, R.3
  • 62
    • 0035876393 scopus 로고    scopus 로고
    • Phase II study of paclitaxel and valspodar (PSC 833) in refractory ovarian carcinoma: A gynecologic oncology group study
    • Fracasso PM, Brady MF, Moore DH et al. Phase II study of paclitaxel and valspodar (PSC 833) in refractory ovarian carcinoma: a gynecologic oncology group study. J. Clin. Oncol. 19(12), 2975-2982 (2001).
    • (2001) J. Clin. Oncol , vol.19 , Issue.12 , pp. 2975-2982
    • Fracasso, P.M.1    Brady, M.F.2    Moore, D.H.3
  • 63
    • 0037194348 scopus 로고    scopus 로고
    • Protein expression profiles indicative for drug resistance of non-small cell lung cancer
    • Volm M, Koomagi R, Mattern J, Efferth T. Protein expression profiles indicative for drug resistance of non-small cell lung cancer. Br. J. Cancer 87(3), 251-257 (2002).
    • (2002) Br. J. Cancer , vol.87 , Issue.3 , pp. 251-257
    • Volm, M.1    Koomagi, R.2    Mattern, J.3    Efferth, T.4
  • 64
    • 21044442673 scopus 로고    scopus 로고
    • Multidrug resistance markers P-glycoprotein, multidrug resistance protein 1, and lung resistance protein in non-small cell lung cancer: Prognostic implications
    • Berger W, Setinek U, Hollaus P et al. Multidrug resistance markers P-glycoprotein, multidrug resistance protein 1, and lung resistance protein in non-small cell lung cancer: prognostic implications. J. Cancer Res. Clin. Oncol. 131(6), 355-363 (2005).
    • (2005) J. Cancer Res. Clin. Oncol , vol.131 , Issue.6 , pp. 355-363
    • Berger, W.1    Setinek, U.2    Hollaus, P.3
  • 65
    • 0031044681 scopus 로고    scopus 로고
    • The clinical role of MDR1 gene expression in human lung cancer, 171B, 721-724
    • Oka M, Fukuda M, Sakamoto A et al. The clinical role of MDR1 gene expression in human lung cancer. Anticancer Res. 17(1B), 721-724 (1997).
    • (1997) Anticancer Res
    • Oka, M.1    Fukuda, M.2    Sakamoto, A.3
  • 66
    • 0026589781 scopus 로고
    • Study of multidrug resistance (MdrI) gene in non-small-cell lung cancer
    • Shin HJ, Lee JS, Hong WK, Shin DM. Study of multidrug resistance (MdrI) gene in non-small-cell lung cancer. Anticancer Res. 12(2), 367-370 (1992).
    • (1992) Anticancer Res , vol.12 , Issue.2 , pp. 367-370
    • Shin, H.J.1    Lee, J.S.2    Hong, W.K.3    Shin, D.M.4
  • 67
    • 0028020860 scopus 로고
    • Quinidine as a resistance modulator of epirubicin in advanced breast cancer: Mature results of a placebo-controlled randomized triat
    • Wishart GC, Bissett D, Paul J et al. Quinidine as a resistance modulator of epirubicin in advanced breast cancer: mature results of a placebo-controlled randomized triat. J. Clin. Oncol. 12(9), 1771-1777 (1994).
    • (1994) J. Clin. Oncol , vol.12 , Issue.9 , pp. 1771-1777
    • Wishart, G.C.1    Bissett, D.2    Paul, J.3
  • 68
    • 7344227279 scopus 로고    scopus 로고
    • Quinine improves the results of intensive chemotherapy in myelodysplastic syndromes expressing P glycoprotein: Results of a randomized study
    • Wattel E, Solary E, Hecquet B et al. Quinine improves the results of intensive chemotherapy in myelodysplastic syndromes expressing P glycoprotein: results of a randomized study. Br. J. Haematol. 102(4), 1015-1024 (1998).
    • (1998) Br. J. Haematol , vol.102 , Issue.4 , pp. 1015-1024
    • Wattel, E.1    Solary, E.2    Hecquet, B.3
  • 69
    • 0032619948 scopus 로고    scopus 로고
    • Quinine improves results of intensive chemotherapy (IC) in myelodysplastic syndromes (MDS) expressing P-glycoprotein (PGP). Updated results of a randomized study. Groupe Francais des Myelodysplasies (GFM) and Groupe GOELAMS
    • Wattel E, Solary E, Hecquet B et al. Quinine improves results of intensive chemotherapy (IC) in myelodysplastic syndromes (MDS) expressing P-glycoprotein (PGP). Updated results of a randomized study. Groupe Francais des Myelodysplasies (GFM) and Groupe GOELAMS. Adv. Exp. Med. Biol. 457, 35-46 (1999).
    • (1999) Adv. Exp. Med. Biol , vol.457 , pp. 35-46
    • Wattel, E.1    Solary, E.2    Hecquet, B.3
  • 70
    • 9444257012 scopus 로고    scopus 로고
    • Combination of quinine as a potential reversing agent with mitoxantrone and cytarabine for the treatment of acute leukemias: A randomized multicenter study
    • Solary E, Witz B, Caillot D et al. Combination of quinine as a potential reversing agent with mitoxantrone and cytarabine for the treatment of acute leukemias: a randomized multicenter study. Blood 88(4), 1198-1205 (1996).
    • (1996) Blood , vol.88 , Issue.4 , pp. 1198-1205
    • Solary, E.1    Witz, B.2    Caillot, D.3
  • 71
    • 0043240289 scopus 로고    scopus 로고
    • Quinine as a multidrug resistance inhibitor: A Phase 3 multicentric randomized study in adult de novo acute myelogenous leukemia
    • Solary E, Drenou B, Campos L et al. Quinine as a multidrug resistance inhibitor: a Phase 3 multicentric randomized study in adult de novo acute myelogenous leukemia. Blood 102(4), 1202-1210 (2003).
    • (2003) Blood , vol.102 , Issue.4 , pp. 1202-1210
    • Solary, E.1    Drenou, B.2    Campos, L.3
  • 72
    • 0031963639 scopus 로고    scopus 로고
    • Results of a Phase III double blind placebo controlled trial of megestrol acetate modulation of P-glycoprotein mediated drug resistance in the first line management of small cell lung carcinoma
    • Wood L. Results of a Phase III double blind placebo controlled trial of megestrol acetate modulation of P-glycoprotein mediated drug resistance in the first line management of small cell lung carcinoma. Br. J. Cancer 77, 627-631 (1998).
    • (1998) Br. J. Cancer , vol.77 , pp. 627-631
    • Wood, L.1
  • 73
    • 0027256051 scopus 로고
    • Oral verapamil with chemotherapy for advanced non-small cell lung cancer: A randomised study
    • Millward MJ, Cantwell BM, Munro NC, Robinson A, Corris PA, Harris AL. Oral verapamil with chemotherapy for advanced non-small cell lung cancer: a randomised study. Br. J. Cancer 67(5), 1031-1035 (1993).
    • (1993) Br. J. Cancer , vol.67 , Issue.5 , pp. 1031-1035
    • Millward, M.J.1    Cantwell, B.M.2    Munro, N.C.3    Robinson, A.4    Corris, P.A.5    Harris, A.L.6
  • 74
    • 0027375301 scopus 로고
    • A randomised clinical study of verapamil in addition to combination chemotherapy in small cell lung cancer. West of Scotland Lung Cancer Research Group, and the Aberdeen Oncology Group
    • Milroy R. A randomised clinical study of verapamil in addition to combination chemotherapy in small cell lung cancer. West of Scotland Lung Cancer Research Group, and the Aberdeen Oncology Group. Br. J. Cancer 68(4), 813-818 (1993).
    • (1993) Br. J. Cancer , vol.68 , Issue.4 , pp. 813-818
    • Milroy, R.1
  • 75
    • 0028816350 scopus 로고
    • A Phase III randomized study of oral verapamil as a chemosensitizer to reverse drug resistance in patients with refractory myeloma. A Southwest Oncology Group study
    • Dalton WS, Crowley JJ, Salmon SS et al. A Phase III randomized study of oral verapamil as a chemosensitizer to reverse drug resistance in patients with refractory myeloma. A Southwest Oncology Group study. Cancer 75(3), 815-820 (1995).
    • (1995) Cancer , vol.75 , Issue.3 , pp. 815-820
    • Dalton, W.S.1    Crowley, J.J.2    Salmon, S.S.3
  • 76
    • 0033635917 scopus 로고    scopus 로고
    • Verapamil increases the survival of patients with anthracycline-resistant metastatic breast carcinoma
    • Belpomme D, Gauthier S, Pujade-Lauraine E et al. Verapamil increases the survival of patients with anthracycline-resistant metastatic breast carcinoma. Ann. Oncol. 11(11), 1471-1476 (2000).
    • (2000) Ann. Oncol , vol.11 , Issue.11 , pp. 1471-1476
    • Belpomme, D.1    Gauthier, S.2    Pujade-Lauraine, E.3
  • 77
    • 0034988112 scopus 로고    scopus 로고
    • Comparison of 'sequential' versus 'standard' chemotherapy as re-induction treatment, with or without cyclosporine, in refractory/relapsed acute myeloid leukaemia (AML): Results of the UK Medical Research Council AML-R trial
    • Liu Yin JA, Wheatley K, Rees JK, Burnett AK. Comparison of 'sequential' versus 'standard' chemotherapy as re-induction treatment, with or without cyclosporine, in refractory/relapsed acute myeloid leukaemia (AML): results of the UK Medical Research Council AML-R trial. Br. J. Haematol. 113(3), 713-726 (2001).
    • (2001) Br. J. Haematol , vol.113 , Issue.3 , pp. 713-726
    • Liu Yin, J.A.1    Wheatley, K.2    Rees, J.K.3    Burnett, A.K.4
  • 78
    • 0035760302 scopus 로고    scopus 로고
    • Benefit of cyclosporine modulation of drug resistance in patients with poor-risk acute myeloid leukemia: A Southwest Oncology Group study
    • List AF, Kopecky KJ, Willman CL et al. Benefit of cyclosporine modulation of drug resistance in patients with poor-risk acute myeloid leukemia: a Southwest Oncology Group study. Blood 98(12), 3212-3220 (2001).
    • (2001) Blood , vol.98 , Issue.12 , pp. 3212-3220
    • List, A.F.1    Kopecky, K.J.2    Willman, C.L.3
  • 79
    • 0035051187 scopus 로고    scopus 로고
    • MDR-1 expression and deletions of chromosomes 7 and 5(Q) separately indicate adverse prognosis in AML
    • Baldus C, Fietz T, Rieder H, Schwartz S, Thiel E, Knauf W. MDR-1 expression and deletions of chromosomes 7 and 5(Q) separately indicate adverse prognosis in AML. Leuk. Lymphoma 40(5-6), 613-623 (2001).
    • (2001) Leuk. Lymphoma , vol.40 , Issue.5-6 , pp. 613-623
    • Baldus, C.1    Fietz, T.2    Rieder, H.3    Schwartz, S.4    Thiel, E.5    Knauf, W.6
  • 80
    • 27144508406 scopus 로고    scopus 로고
    • The value of the MDR1 reversal agent PSC-933 in addition to daunorubicin and cytarabine in the treatment of elderly patients with previously untreated acute myeloid leukemia (AML), in relation to MDR1 status at diagnosis
    • van der Holt B, Lowenberg B, Burnett AK et al. The value of the MDR1 reversal agent PSC-933 in addition to daunorubicin and cytarabine in the treatment of elderly patients with previously untreated acute myeloid leukemia (AML), in relation to MDR1 status at diagnosis. Blood 106(8), 2646-2654 (2005).
    • (2005) Blood , vol.106 , Issue.8 , pp. 2646-2654
    • van der Holt, B.1    Lowenberg, B.2    Burnett, A.K.3
  • 81
    • 0037103189 scopus 로고    scopus 로고
    • Phase 3 study of the multidrug resistance modulator PSC-833 in previously untreated patients 60 years of age and older with acute myeloid leukemia: Cancer and Leukemia Group B Study 9720
    • Baer MR, George SL, Dodge RK et al. Phase 3 study of the multidrug resistance modulator PSC-833 in previously untreated patients 60 years of age and older with acute myeloid leukemia: Cancer and Leukemia Group B Study 9720. Blood 100(4), 1224-1232 (2002).
    • (2002) Blood , vol.100 , Issue.4 , pp. 1224-1232
    • Baer, M.R.1    George, S.L.2    Dodge, R.K.3
  • 82
    • 16544385074 scopus 로고    scopus 로고
    • Dose escalation studies of cytarabine, daunorubicin, and etoposide with and without multidrug resistance modulation with PSC-833 in untreated adults with acute myeloid leukemia younger than 60 years: Final induction results of Cancer and Leukemia Group B Study 9621
    • Kolitz JE, George SL, Dodge RK et al. Dose escalation studies of cytarabine, daunorubicin, and etoposide with and without multidrug resistance modulation with PSC-833 in untreated adults with acute myeloid leukemia younger than 60 years: final induction results of Cancer and Leukemia Group B Study 9621. J. Clin. Oncol, 22(21), 4290-4301 (2004).
    • (2004) J. Clin. Oncol , vol.22 , Issue.21 , pp. 4290-4301
    • Kolitz, J.E.1    George, S.L.2    Dodge, R.K.3
  • 83
    • 0003360972 scopus 로고    scopus 로고
    • A Phase 3 study of PSC833 in combination with paclitaxel and carboplatin alone in patients with stage IV or suboptimally debulked stage III epithelial ovarian cancer or primary cancer of the peritoneum
    • Abstract 806
    • Joly F et al. A Phase 3 study of PSC833 in combination with paclitaxel and carboplatin alone in patients with stage IV or suboptimally debulked stage III epithelial ovarian cancer or primary cancer of the peritoneum. Proc. Am. Soc. Clin. Oncol., 21, (2002) (Abstract 806).
    • (2002) Proc. Am. Soc. Clin. Oncol , vol.21
    • Joly, F.1
  • 84
  • 85
    • 0036569569 scopus 로고    scopus 로고
    • A Phase II trial of combination chemotherapy and surgical resection for the treatment of metastatic adrenocortical carcinoma: Continuous infusion doxorubicin, vincristine, and etoposide with daily mitotane as a P-glycoprotein antagonist
    • Abraham J, Bakke S, Rutt A et al. A Phase II trial of combination chemotherapy and surgical resection for the treatment of metastatic adrenocortical carcinoma: continuous infusion doxorubicin, vincristine, and etoposide with daily mitotane as a P-glycoprotein antagonist. Cancer 94(9), 2333-2343 (2002).
    • (2002) Cancer , vol.94 , Issue.9 , pp. 2333-2343
    • Abraham, J.1    Bakke, S.2    Rutt, A.3
  • 86
    • 0037478891 scopus 로고    scopus 로고
    • Increased penetration of paclitaxel into the brain by inhibition of P-Glycoprotein
    • Kemper EM, van Zandbergen AE, Cleypool C et al. Increased penetration of paclitaxel into the brain by inhibition of P-Glycoprotein. Clin. Cancer Res. 9(7), 2849-2855 (2003).
    • (2003) Clin. Cancer Res , vol.9 , Issue.7 , pp. 2849-2855
    • Kemper, E.M.1    van Zandbergen, A.E.2    Cleypool, C.3
  • 87
    • 0442313667 scopus 로고    scopus 로고
    • The influence of the P-glycoprotein inhibitor zosuquidar trihydrochloride (LY335979) on the brain penetration of paclitaxel in mice
    • Kemper EM, Cleypool C, Boogerd W, Beijnen JH, van Tellingen O. The influence of the P-glycoprotein inhibitor zosuquidar trihydrochloride (LY335979) on the brain penetration of paclitaxel in mice. Cancer Chemother. Pharmacol. 53(2), 173-178 (2004).
    • (2004) Cancer Chemother. Pharmacol , vol.53 , Issue.2 , pp. 173-178
    • Kemper, E.M.1    Cleypool, C.2    Boogerd, W.3    Beijnen, J.H.4    van Tellingen, O.5
  • 88
    • 0029836316 scopus 로고    scopus 로고
    • Role of P-glycoprotein in the blood-brain transport of colchicine and vinblastine
    • Drion N, Lemaire M, Lefauconnier JM, Scherrmann JM. Role of P-glycoprotein in the blood-brain transport of colchicine and vinblastine. J. Neurochem. 67(4), 1688-1693 (1996).
    • (1996) J. Neurochem , vol.67 , Issue.4 , pp. 1688-1693
    • Drion, N.1    Lemaire, M.2    Lefauconnier, J.M.3    Scherrmann, J.M.4
  • 89
    • 0033977493 scopus 로고    scopus 로고
    • Effect of P-glycoprotein modulation with cyclosporin A on cerebrospinal fluid penetration of doxorubicin in non-human primates
    • Warren KE, Patel MC, McCully CM, Montuenga LM, Balis FM. Effect of P-glycoprotein modulation with cyclosporin A on cerebrospinal fluid penetration of doxorubicin in non-human primates. Cancer Chemother. Pharmacol. 45(3), 207-212 (2000).
    • (2000) Cancer Chemother. Pharmacol , vol.45 , Issue.3 , pp. 207-212
    • Warren, K.E.1    Patel, M.C.2    McCully, C.M.3    Montuenga, L.M.4    Balis, F.M.5
  • 90
    • 0031907402 scopus 로고    scopus 로고
    • Modulation of doxorubicin concentration by cyclosporin A in brain and testicular barrier tissues expressing P-glycoprotein in rats
    • Hughes CS, Vaden SL, Manaugh CA, Price GS, Hudson LC. Modulation of doxorubicin concentration by cyclosporin A in brain and testicular barrier tissues expressing P-glycoprotein in rats. J. Neurooncol. 37(1), 45-54 (1998).
    • (1998) J. Neurooncol , vol.37 , Issue.1 , pp. 45-54
    • Hughes, C.S.1    Vaden, S.L.2    Manaugh, C.A.3    Price, G.S.4    Hudson, L.C.5
  • 91
    • 0036128985 scopus 로고    scopus 로고
    • Role of multidrug transporters in pharmacoresistance to antiepileptic drugs
    • Loscher W, Potschka H. Role of multidrug transporters in pharmacoresistance to antiepileptic drugs. J. Pharmacol. Exp. Ther. 301(1), 7-14 (2002).
    • (2002) J. Pharmacol. Exp. Ther , vol.301 , Issue.1 , pp. 7-14
    • Loscher, W.1    Potschka, H.2
  • 92
    • 0037178642 scopus 로고    scopus 로고
    • P-glycoprotein-mediated efflux of phenobarbital, lamotrigine, and felbamate at the blood-brain barrier: Evidence from microdialysis experiments in rats
    • Potschka H, Fedrowitz M, Loscher W. P-glycoprotein-mediated efflux of phenobarbital, lamotrigine, and felbamate at the blood-brain barrier: evidence from microdialysis experiments in rats. Neurosci. Lett. 327(3), 173-176 (2002).
    • (2002) Neurosci. Lett , vol.327 , Issue.3 , pp. 173-176
    • Potschka, H.1    Fedrowitz, M.2    Loscher, W.3
  • 93
    • 0037148065 scopus 로고    scopus 로고
    • A comparison of extracellular levels of phenytoin in amygdala and hippocampus of kindled and non-kindled rats
    • Potschka H, Loscher W. A comparison of extracellular levels of phenytoin in amygdala and hippocampus of kindled and non-kindled rats. Neuroreport 13(1), 167-171 (2002).
    • (2002) Neuroreport , vol.13 , Issue.1 , pp. 167-171
    • Potschka, H.1    Loscher, W.2
  • 94
    • 33645513798 scopus 로고    scopus 로고
    • Inhibition of the multidrug transporter P-glycoprotein improves seizure control in phenytoin-treated chronic epileptic rats
    • van Vliet EA, van Schaik R, Edelbroek PM et al. Inhibition of the multidrug transporter P-glycoprotein improves seizure control in phenytoin-treated chronic epileptic rats. Epilepsia 47(4), 672-680 (2006).
    • (2006) Epilepsia , vol.47 , Issue.4 , pp. 672-680
    • van Vliet, E.A.1    van Schaik, R.2    Edelbroek, P.M.3
  • 95
    • 33748792802 scopus 로고    scopus 로고
    • The multidrug transporter hypothesis of drug resistance in epilepsy: Proof-of-principle in a rat model of temporal lobe epilepsy
    • Brandt C, Bethmann K, Gastens AM, Loscher W. The multidrug transporter hypothesis of drug resistance in epilepsy: proof-of-principle in a rat model of temporal lobe epilepsy. Neurobiol. Dis. 24(1), 202-211 (2006).
    • (2006) Neurobiol. Dis , vol.24 , Issue.1 , pp. 202-211
    • Brandt, C.1    Bethmann, K.2    Gastens, A.M.3    Loscher, W.4
  • 96
    • 0034121122 scopus 로고    scopus 로고
    • Pharmacological inhibition of P-glycoprotein transport enhances the distribution of HIV-1 protease inhibitors into brain and testes
    • Choo EF, Leake B, Wandel C et al. Pharmacological inhibition of P-glycoprotein transport enhances the distribution of HIV-1 protease inhibitors into brain and testes. Drug Metab. Dispos. 28(6), 655-660 (2000).
    • (2000) Drug Metab. Dispos , vol.28 , Issue.6 , pp. 655-660
    • Choo, E.F.1    Leake, B.2    Wandel, C.3
  • 97
    • 0037372771 scopus 로고    scopus 로고
    • Effect of efflux inhibition on brain uptake of itraconazole in mice infected with Cryptococcus neoformans
    • Imbert F, Jardin M, Fernandez C et al. Effect of efflux inhibition on brain uptake of itraconazole in mice infected with Cryptococcus neoformans. Drug Metab. Dispos. 31(3), 319-325 (2003).
    • (2003) Drug Metab. Dispos , vol.31 , Issue.3 , pp. 319-325
    • Imbert, F.1    Jardin, M.2    Fernandez, C.3
  • 98
    • 0035984821 scopus 로고    scopus 로고
    • GF120918, a P-glycoprotein modulator, increases the concentration of unbound amprenavir in the central nervous system in rats
    • Edwards JE, Brouwer KR, McNamara PJ. GF120918, a P-glycoprotein modulator, increases the concentration of unbound amprenavir in the central nervous system in rats. Antimicrob. Agents Chemother. 46(7), 2284-2286 (2002).
    • (2002) Antimicrob. Agents Chemother , vol.46 , Issue.7 , pp. 2284-2286
    • Edwards, J.E.1    Brouwer, K.R.2    McNamara, P.J.3
  • 99
    • 0036237761 scopus 로고    scopus 로고
    • Effects of a P-glycoprotein inhibitor on brain and plasma concentrations of anti-human immunodeficiency virus drugs administered in combination in rats
    • Savolainen J, Edwards JE, Morgan ME, McNamara PJ, Anderson BD. Effects of a P-glycoprotein inhibitor on brain and plasma concentrations of anti-human immunodeficiency virus drugs administered in combination in rats. Drug Metab. Dispos. 30(5), 479-482 (2002).
    • (2002) Drug Metab. Dispos , vol.30 , Issue.5 , pp. 479-482
    • Savolainen, J.1    Edwards, J.E.2    Morgan, M.E.3    McNamara, P.J.4    Anderson, B.D.5
  • 100
    • 0033833430 scopus 로고    scopus 로고
    • Increased drug delivery to the brain by P-glycoprotein inhibition
    • Sadeque AJ, Wandel C, He H, Shah S, Wood AJ. Increased drug delivery to the brain by P-glycoprotein inhibition. Clin. Pharmacol. Ther. 68(3), 231-237 (2000).
    • (2000) Clin. Pharmacol. Ther , vol.68 , Issue.3 , pp. 231-237
    • Sadeque, A.J.1    Wandel, C.2    He, H.3    Shah, S.4    Wood, A.J.5
  • 101
    • 33646790191 scopus 로고    scopus 로고
    • Differential in vivo sensitivity to inhibition of P-glycoprotein located in lymphocytes, testes, and the blood-brain barrier
    • Choo EF, Kurnik D, Muszkat M et al. Differential in vivo sensitivity to inhibition of P-glycoprotein located in lymphocytes, testes, and the blood-brain barrier. J. Pharmacol Exp. Ther. 317(3), 1012-1018 (2006).
    • (2006) J. Pharmacol Exp. Ther , vol.317 , Issue.3 , pp. 1012-1018
    • Choo, E.F.1    Kurnik, D.2    Muszkat, M.3
  • 102
    • 0036799701 scopus 로고    scopus 로고
    • Increased CNS uptake and enhanced antinociception of morphine-6-glucuronide in rats after inhibition of P-glycoprotein
    • Lotsch J. Schmidt R, Vetter G et al. Increased CNS uptake and enhanced antinociception of morphine-6-glucuronide in rats after inhibition of P-glycoprotein. J. Neurochem. 83(2), 241-248 (2002).
    • (2002) J. Neurochem , vol.83 , Issue.2 , pp. 241-248
    • Lotsch, J.1    Schmidt, R.2    Vetter, G.3
  • 103
    • 0030781139 scopus 로고    scopus 로고
    • Full blockade of intestinal P-glycoprotein and extensive inhibition of blood-brain barrier P-glycoprotein by oral treatment of mice with PSC833
    • Mayer U, Wagenaar E, Dorobek B. Beijnen JH, Borst P, Schinkel AH. Full blockade of intestinal P-glycoprotein and extensive inhibition of blood-brain barrier P-glycoprotein by oral treatment of mice with PSC833. J. Clin. Invest. 100(10), 2430-2436 (1997).
    • (1997) J. Clin. Invest , vol.100 , Issue.10 , pp. 2430-2436
    • Mayer, U.1    Wagenaar, E.2    Dorobek, B.3    Beijnen, J.H.4    Borst, P.5    Schinkel, A.H.6
  • 105
    • 0035017246 scopus 로고    scopus 로고
    • Multidrug resistance P-glycoprotein hampers the access of cortisol but not of corticosterone to mouse and human brain
    • Karssen AM, Meijer OC, van der Sandt IC et al. Multidrug resistance P-glycoprotein hampers the access of cortisol but not of corticosterone to mouse and human brain. Endocrinology 142(6), 2686-2694 (2001).
    • (2001) Endocrinology , vol.142 , Issue.6 , pp. 2686-2694
    • Karssen, A.M.1    Meijer, O.C.2    van der Sandt, I.C.3
  • 106
    • 33750824249 scopus 로고    scopus 로고
    • Determinants of drug brain uptake in a rat model of seizure-associated malformations of cortical development
    • Marchi N, Guiso G, Caccia S et al. Determinants of drug brain uptake in a rat model of seizure-associated malformations of cortical development. Neurobiol. Dis. 24(3), 429-442 (2006).
    • (2006) Neurobiol. Dis , vol.24 , Issue.3 , pp. 429-442
    • Marchi, N.1    Guiso, G.2    Caccia, S.3


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