메뉴 건너뛰기




Volumn 9, Issue 7, 2003, Pages 2849-2855

Increased penetration of paclitaxel into the brain by inhibition of P-glycoprotein

Author keywords

[No Author keywords available]

Indexed keywords

CREMOPHOR; CYCLOSPORIN A; ELACRIDAR; GLYCOPROTEIN P; PACLITAXEL; PROTEIN INHIBITOR; VALSPODAR;

EID: 0037478891     PISSN: 10780432     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (241)

References (40)
  • 1
    • 0030588582 scopus 로고    scopus 로고
    • Reconstitution of the blood-brain barrier in cell culture for studies of drug transport and metabolism
    • De Boer, A. G., and Breimer, D. D. Reconstitution of the blood-brain barrier in cell culture for studies of drug transport and metabolism. Adv. Drug Delivery Rev., 22: 251-264, 1996.
    • (1996) Adv. Drug Delivery Rev. , vol.22 , pp. 251-264
    • De Boer, A.G.1    Breimer, D.D.2
  • 2
    • 0019124032 scopus 로고
    • Relationship of octanol/water partition coefficient and molecular weight to rat brain capillary permeability
    • Levin, V. A. Relationship of octanol/water partition coefficient and molecular weight to rat brain capillary permeability. J. Med. Chem., 23: 682-684, 1980.
    • (1980) J. Med. Chem. , vol.23 , pp. 682-684
    • Levin, V.A.1
  • 3
    • 0028158735 scopus 로고
    • A method to determine the ability of drugs to diffuse through the blood-brain barrier
    • Seelig, A., Gottschlich, R., and Devant, R. M. A method to determine the ability of drugs to diffuse through the blood-brain barrier. Proc. Natl. Acad. Sci. USA, 91: 68-72, 1994.
    • (1994) Proc. Natl. Acad. Sci. USA , vol.91 , pp. 68-72
    • Seelig, A.1    Gottschlich, R.2    Devant, R.M.3
  • 5
    • 0029770135 scopus 로고    scopus 로고
    • MDR1 P-glycoprotein is expressed by endothelial cells of newly formed capillaries in human gliomas but is not expressed in the neovasculature of other primary tumors
    • Toth, K., Vaughan, M. M., Peress, N. S., Slocum, H. K., and Rustum, Y. M. MDR1 P-glycoprotein is expressed by endothelial cells of newly formed capillaries in human gliomas but is not expressed in the neovasculature of other primary tumors. Am. J. Pathol., 149: 853-858, 1996.
    • (1996) Am. J. Pathol. , vol.149 , pp. 853-858
    • Toth, K.1    Vaughan, M.M.2    Peress, N.S.3    Slocum, H.K.4    Rustum, Y.M.5
  • 6
    • 0030823912 scopus 로고    scopus 로고
    • P-glycoprotein is strongly expressed in the luminal membranes of the endothelium of blood vessels in the brain
    • Beaulieu, E., Demeule, M., Ghitescu, L., and Beliveau, R. P-glycoprotein is strongly expressed in the luminal membranes of the endothelium of blood vessels in the brain. Biochem. J., 326: 539-544, 1997.
    • (1997) Biochem. J. , vol.326 , pp. 539-544
    • Beaulieu, E.1    Demeule, M.2    Ghitescu, L.3    Beliveau, R.4
  • 7
    • 0020578356 scopus 로고
    • Cell surface P-glycoprotein associated with multidrug resistance in mammalian cell lines
    • Kartner, N., Riordan, J. R., and Ling, V. Cell surface P-glycoprotein associated with multidrug resistance in mammalian cell lines. Science (Wash. DC), 221: 1285-1288, 1983.
    • (1983) Science (Wash. DC) , vol.221 , pp. 1285-1288
    • Kartner, N.1    Riordan, J.R.2    Ling, V.3
  • 8
    • 0025071180 scopus 로고
    • Expression of the multidrug resistance gene product (P-glycoprotein) in human normal and tumor tissues
    • Cordon-Cardo, C., O'Brien, J. P., Boccia, J., Casals, D., Bertino, J. R., and Melamed, M. R. Expression of the multidrug resistance gene product (P-glycoprotein) in human normal and tumor tissues. J. Histochem. Cytochem., 38: 1277-1287, 1990.
    • (1990) J. Histochem. Cytochem. , vol.38 , pp. 1277-1287
    • Cordon-Cardo, C.1    O'Brien, J.P.2    Boccia, J.3    Casals, D.4    Bertino, J.R.5    Melamed, M.R.6
  • 10
    • 0029892497 scopus 로고    scopus 로고
    • P-glycoprotein in the blood-brain barrier of mice influences the brain penetration and pharmacological activity of many drugs
    • Schinkel, A. H., Wagenaar, E., Mol, C. A. A. M., and van Deemter, L. P-glycoprotein in the blood-brain barrier of mice influences the brain penetration and pharmacological activity of many drugs. J. Clin. Investig., 97: 2517-2524, 1996.
    • (1996) J. Clin. Investig. , vol.97 , pp. 2517-2524
    • Schinkel, A.H.1    Wagenaar, E.2    Mol, C.A.A.M.3    Van Deemter, L.4
  • 12
    • 0030922974 scopus 로고    scopus 로고
    • Multidrug resistance-reversing agents increase vinblastine distribution in normal tissues expressing the P-glycoprotein but do not enhance drug penetration in brain and testis
    • Arboix, M., Paz, O. G., Colombo, T., and Dincalci, M. Multidrug resistance-reversing agents increase vinblastine distribution in normal tissues expressing the P-glycoprotein but do not enhance drug penetration in brain and testis. J. Pharmacol. Exp. Ther., 281: 1226-1230, 1997.
    • (1997) J. Pharmacol. Exp. Ther. , vol.281 , pp. 1226-1230
    • Arboix, M.1    Paz, O.G.2    Colombo, T.3    Dincalci, M.4
  • 13
    • 0030788302 scopus 로고    scopus 로고
    • New multidrug-resistance-reversing drugs, MS-209 and SDZ PSC 833
    • Naito, M., and Tsuruo, T. New multidrug-resistance-reversing drugs, MS-209 and SDZ PSC 833. Cancer Chemother. Pharmacol., 40: S20-S24, 1997.
    • (1997) Cancer Chemother. Pharmacol. , vol.40
    • Naito, M.1    Tsuruo, T.2
  • 14
    • 0027524642 scopus 로고
    • In vitro and in vivo reversal of multidrug resistance by GF120918, an acridonecarboxamide derivative
    • Hyafil, F., Vergely, C., Du Vignaud, P., and Grand-Perret, T. In vitro and in vivo reversal of multidrug resistance by GF120918, an acridonecarboxamide derivative. Cancer Res., 53: 4595-4602, 1993.
    • (1993) Cancer Res. , vol.53 , pp. 4595-4602
    • Hyafil, F.1    Vergely, C.2    Du Vignaud, P.3    Grand-Perret, T.4
  • 18
    • 0029616144 scopus 로고
    • Quantification of paclitaxel metabolites in human plasma by high-performance liquid chromatography
    • Huizing, M. T., Sparreboom, A., Rosing, H., van Tellingen, O., Pinedo, H. M., and Beijnen, J. H. Quantification of paclitaxel metabolites in human plasma by high-performance liquid chromatography. J. Chromatogr. B, 674: 261-268, 1995.
    • (1995) J. Chromatogr. B , vol.674 , pp. 261-268
    • Huizing, M.T.1    Sparreboom, A.2    Rosing, H.3    Van Tellingen, O.4    Pinedo, H.M.5    Beijnen, J.H.6
  • 20
    • 0035812216 scopus 로고    scopus 로고
    • Bioanalysis and preliminary pharmacokinetics of the acridonecarboxamide derivative GF120918 in plasma of mice and humans by ion-pairing reversed-phase high-performance liquid chromatography with fluorescence detection
    • Kemper, E. M., Jansen, B., Brouwer, K. R., Schellens, J. H. M., Beijnen, J. H., and van Tellingen, O. Bioanalysis and preliminary pharmacokinetics of the acridonecarboxamide derivative GF120918 in plasma of mice and humans by ion-pairing reversed-phase high-performance liquid chromatography with fluorescence detection. J. Chromatogr. B, 759: 135-143, 2001.
    • (2001) J. Chromatogr. B , vol.759 , pp. 135-143
    • Kemper, E.M.1    Jansen, B.2    Brouwer, K.R.3    Schellens, J.H.M.4    Beijnen, J.H.5    Van Tellingen, O.6
  • 21
    • 0029973751 scopus 로고    scopus 로고
    • Determination of polyoxyethyleneglycerol triricinoleate 35 (Cremophor EL) in plasma by pre-column derivatization and reversed-phase high-performance liquid chromatography
    • Sparreboom, A., van Tellingen, O., Huizing, M. T., Nooijen, W. J., and Beijnen, J. H. Determination of polyoxyethyleneglycerol triricinoleate 35 (Cremophor EL) in plasma by pre-column derivatization and reversed-phase high-performance liquid chromatography. J. Chromatogr. B, 681: 355-362, 1996.
    • (1996) J. Chromatogr. B , vol.681 , pp. 355-362
    • Sparreboom, A.1    Van Tellingen, O.2    Huizing, M.T.3    Nooijen, W.J.4    Beijnen, J.H.5
  • 23
    • 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, J. H., Borst, P., and Schinkel, A. H. Full blockade of intestinal P-glycoprotein and extensive inhibition of blood-brain barrier P-glycoprotein by oral treatment of mice with PSC833. J. Clin. Investig., 100: 2430-2436, 1997.
    • (1997) J. Clin. Investig. , vol.100 , pp. 2430-2436
    • Mayer, U.1    Wagenaar, E.2    Dorobek, B.3    Beijnen, J.H.4    Borst, P.5    Schinkel, A.H.6
  • 24
    • 0029836316 scopus 로고    scopus 로고
    • Role of P-glycoprotein in the blood-brain transport of colchicine and vinblastine
    • Drion, N., Lemaire, M., Lefauconnier, J. M., and Scherrmann, J. M. Role of P-glycoprotein in the blood-brain transport of colchicine and vinblastine. J. Neurochem., 67: 1688-1693, 1996.
    • (1996) J. Neurochem. , vol.67 , pp. 1688-1693
    • Drion, N.1    Lemaire, M.2    Lefauconnier, J.M.3    Scherrmann, J.M.4
  • 25
    • 0031946026 scopus 로고    scopus 로고
    • Effect of GF120918, a potent P-glycoprotein inhibitor, on morphine pharmacokinetics and pharmacodynamics in the rat
    • Letrent, S. P., Pollack, G. M., Brouwer, K. R., and Brouwer, K. L. R. Effect of GF120918, a potent P-glycoprotein inhibitor, on morphine pharmacokinetics and pharmacodynamics in the rat. Pharm. Res. (N. Y.), 15: 599-605, 1998.
    • (1998) Pharm. Res. (N. Y.) , vol.15 , pp. 599-605
    • Letrent, S.P.1    Pollack, G.M.2    Brouwer, K.R.3    Brouwer, K.L.R.4
  • 26
    • 0022495689 scopus 로고
    • Cyclosporin A corrects daunorubicin resistance in Ehrlich ascites carcinoma
    • Slater, L. M., Sweet, P., Stupecky, M., Wetzel, M. W., and Gupta, S. Cyclosporin A corrects daunorubicin resistance in Ehrlich ascites carcinoma. Br. J. Cancer, 54: 235-238, 1986.
    • (1986) Br. J. Cancer , vol.54 , pp. 235-238
    • Slater, L.M.1    Sweet, P.2    Stupecky, M.3    Wetzel, M.W.4    Gupta, S.5
  • 27
    • 0026453343 scopus 로고
    • Cyclosporin A potentiation of VP-16: Production of long-term survival in murine acute lymphatic leukemia
    • Slater, L. M., Cho, J., and Wetzel, M. Cyclosporin A potentiation of VP-16: production of long-term survival in murine acute lymphatic leukemia. Cancer Chemother. Pharmacol., 31: 53-56, 1992.
    • (1992) Cancer Chemother. Pharmacol. , vol.31 , pp. 53-56
    • Slater, L.M.1    Cho, J.2    Wetzel, M.3
  • 34
    • 0038582891 scopus 로고    scopus 로고
    • XR9576 (tariquidar), a potent and specific P-glycoprotein inhibitor, has minimal effects on the pharmacokinetics of paclitaxel, doxorubicin, and vinorelbine and can be administered with full-dose chemotherapy in patients with cancer
    • Boniface, G. R., Ferry, D., Atsmon, J., Inbar, M., van Tellingen, O., Abraham, J., Bates, S. E., Fojo, T., Thomas, H., Mould, G., Steiner, J., and Mellows, G. XR9576 (tariquidar), a potent and specific P-glycoprotein 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., 39: 2173, 2002.
    • (2002) Proc. Am. Soc. Clin. Oncol. , vol.39 , pp. 2173
    • Boniface, G.R.1    Ferry, D.2    Atsmon, J.3    Inbar, M.4    Van Tellingen, O.5    Abraham, J.6    Bates, S.E.7    Fojo, T.8    Thomas, H.9    Mould, G.10    Steiner, J.11    Mellows, G.12
  • 35
    • 0033993578 scopus 로고    scopus 로고
    • Phase I study of paclitaxel in combination with a multidrug resistance modulator, PSC 833 (Valspodar), in refractory malignancies
    • Fracasso, P. M., Westerveldt, P., Fears, C. A., Rosen, D. M., Zuhowski, E. G., Cazenave, L. A., Litchman, M., and Egorin, M. J. Phase I study of paclitaxel in combination with a multidrug resistance modulator, PSC 833 (Valspodar), in refractory malignancies. J. Clin. Oncol., 18: 1124-1135, 2000.
    • (2000) J. Clin. Oncol. , vol.18 , pp. 1124-1135
    • Fracasso, P.M.1    Westerveldt, P.2    Fears, C.A.3    Rosen, D.M.4    Zuhowski, E.G.5    Cazenave, L.A.6    Litchman, M.7    Egorin, M.J.8
  • 38
    • 0025325040 scopus 로고
    • Reversal of the multidrug resistance phenotype with cremophor EL, a common vehicle for water-insoluble vitamins and drugs
    • Woodcock, D. M., Jefferson, S., Linsenmeyer, M. E., Crowther, P. J., Chojnowski, G. M., Williams, B., and Bertoncello, I. Reversal of the multidrug resistance phenotype with cremophor EL, a common vehicle for water-insoluble vitamins and drugs. Cancer Res., 50: 4199-4203, 1990.
    • (1990) Cancer Res. , vol.50 , pp. 4199-4203
    • Woodcock, D.M.1    Jefferson, S.2    Linsenmeyer, M.E.3    Crowther, P.J.4    Chojnowski, G.M.5    Williams, B.6    Bertoncello, I.7
  • 40
    • 0029769055 scopus 로고    scopus 로고
    • Cremophor EL reversed multidrug resistance in vitro but not in tumor-bearing mouse models
    • Watanabe, T., Nakayama, Y., Naito, M., Ohhara, T., Itoh, Y., and Tsuruo, T. Cremophor EL reversed multidrug resistance in vitro but not in tumor-bearing mouse models. Anti-Cancer Drugs, 7: 825-832, 1996.
    • (1996) Anti-Cancer Drugs , vol.7 , pp. 825-832
    • Watanabe, T.1    Nakayama, Y.2    Naito, M.3    Ohhara, T.4    Itoh, Y.5    Tsuruo, T.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.