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Volumn 86, Issue 7, 2013, Pages 904-913

Human ABCB1 (P-glycoprotein) and ABCG2 mediate resistance to BI 2536, a potent and selective inhibitor of Polo-like kinase 1

Author keywords

ABC transporter; BI 2536; Multidrug resistance; Polo like kinase 1

Indexed keywords

4 (8 CYCLOPENTYL 7 ETHYL 5,6,7,8 TETRAHYDRO 5 METHYL 6 OXO 2 PTERIDINYLAMINO) 3 METHOXY N (1 METHYL 4 PIPERIDINYL)BENZAMIDE; ABC TRANSPORTER A1; ABC TRANSPORTER G1; ADENOSINE TRIPHOSPHATASE; BREAST CANCER RESISTANCE PROTEIN; LAPATINIB; MULTIDRUG RESISTANCE PROTEIN 1; NILOTINIB; POLO LIKE KINASE 1;

EID: 84884704883     PISSN: 00062952     EISSN: 18732968     Source Type: Journal    
DOI: 10.1016/j.bcp.2013.08.004     Document Type: Article
Times cited : (34)

References (47)
  • 1
    • 43049151493 scopus 로고    scopus 로고
    • Polo on the Rise-from Mitotic Entry to Cytokinesis with Plk1
    • DOI 10.1016/j.devcel.2008.04.014, PII S1534580708001779
    • M. Petronczki, P. Lenart, and J.M. Peters Polo on the rise-from mitotic entry to cytokinesis with Plk1 Dev Cell 14 2008 646 659 (Pubitemid 351622626)
    • (2008) Developmental Cell , vol.14 , Issue.5 , pp. 646-659
    • Petronczki, M.1    Lenart, P.2    Peters, J.-M.3
  • 2
    • 18344366048 scopus 로고    scopus 로고
    • Getting in and out of mitosis with Polo-like kinase-1
    • DOI 10.1038/sj.onc.1208617
    • M.A. van Vugt, and R.H. Medema Getting in and out of mitosis with Polo-like kinase-1 Oncogene 24 2005 2844 2859 (Pubitemid 40638094)
    • (2005) Oncogene , vol.24 , Issue.17 , pp. 2844-2859
    • Van Vugt, M.A.T.M.1    Medema, R.H.2
  • 3
    • 33846523617 scopus 로고    scopus 로고
    • Targeted anti-mitotic therapies: Can we improve on tubulin agents?
    • DOI 10.1038/nrc2049, PII NRC2049
    • J.R. Jackson, D.R. Patrick, M.M. Dar, and P.S. Huang Targeted anti-mitotic therapies: can we improve on tubulin agents Nat Rev Cancer 7 2007 107 117 (Pubitemid 46160987)
    • (2007) Nature Reviews Cancer , vol.7 , Issue.2 , pp. 107-117
    • Jackson, J.R.1    Patrick, D.R.2    Dar, M.M.3    Huang, P.S.4
  • 4
    • 0035826154 scopus 로고    scopus 로고
    • Polo-like kinase 1 phosphorylates cyclin B1 and targets it to the nucleus during prophase
    • DOI 10.1038/35065617
    • F. Toyoshima-Morimoto, E. Taniguchi, N. Shinya, A. Iwamatsu, and E. Nishida Polo-like kinase 1 phosphorylates cyclin B1 and targets it to the nucleus during prophase Nature 410 2001 215 220 (Pubitemid 32216594)
    • (2001) Nature , vol.410 , Issue.6825 , pp. 215-220
    • Toyoshima-Morimoto, F.1    Taniguchi, E.2    Shinya, N.3    Iwamatsu, A.4    Nishida, E.5
  • 5
    • 0030462914 scopus 로고    scopus 로고
    • Antibody microinjection reveals an essential role for human polo-like kinase 1 (Plk1) in the functional maturation of mitotic centrosomes
    • DOI 10.1083/jcb.135.6.1701
    • H.A. Lane, and E.A. Nigg Antibody microinjection reveals an essential role for human Polo-like kinase 1 (Plk1) in the functional maturation of mitotic centrosomes J Cell Biol 135 1996 1701 1713 (Pubitemid 27036434)
    • (1996) Journal of Cell Biology , vol.135 , Issue.6 , pp. 1701-1713
    • Lane, H.A.1    Nigg, E.A.2
  • 7
    • 33746869956 scopus 로고    scopus 로고
    • Polo-like kinase 1: Target and regulator of anaphase-promoting complex/cyclosome-dependent proteolysis
    • DOI 10.1158/0008-5472.CAN-06-0358
    • F. Eckerdt, and K. Strebhardt Polo-like kinase 1: target and regulator of anaphase-promoting complex/cyclosome-dependent proteolysis Cancer Res 66 2006 6895 6898 (Pubitemid 44197661)
    • (2006) Cancer Research , vol.66 , Issue.14 , pp. 6895-6898
    • Eckerdt, F.1    Strebhardt, K.2
  • 9
    • 33645316142 scopus 로고    scopus 로고
    • Targeting Polo-like kinase 1 for cancer therapy
    • K. Strebhardt, and A. Ullrich Targeting Polo-like kinase 1 for cancer therapy Nat Rev Cancer 6 2006 321 330
    • (2006) Nat Rev Cancer , vol.6 , pp. 321-330
    • Strebhardt, K.1    Ullrich, A.2
  • 10
    • 62449333305 scopus 로고    scopus 로고
    • Identification of Polo-like kinase 1 as a potential therapeutic target in anaplastic thyroid carcinoma
    • T.C. Nappi, P. Salerno, H. Zitzelsberger, F. Carlomagno, G. Salvatore, and M. Santoro Identification of Polo-like kinase 1 as a potential therapeutic target in anaplastic thyroid carcinoma Cancer Res 69 2009 1916 1923
    • (2009) Cancer Res , vol.69 , pp. 1916-1923
    • Nappi, T.C.1    Salerno, P.2    Zitzelsberger, H.3    Carlomagno, F.4    Salvatore, G.5    Santoro, M.6
  • 11
    • 70149106223 scopus 로고    scopus 로고
    • Polo-like kinase 1 is overexpressed in acute myeloid leukemia and its inhibition preferentially targets the proliferation of leukemic cells
    • A.G. Renner, C. Dos Santos, C. Recher, C. Bailly, L. Creancier, and A. Kruczynski Polo-like kinase 1 is overexpressed in acute myeloid leukemia and its inhibition preferentially targets the proliferation of leukemic cells Blood 114 2009 659 662
    • (2009) Blood , vol.114 , pp. 659-662
    • Renner, A.G.1    Dos Santos, C.2    Recher, C.3    Bailly, C.4    Creancier, L.5    Kruczynski, A.6
  • 12
    • 76749159360 scopus 로고    scopus 로고
    • Polo-like kinase 1 (Plk1) as a novel drug target in chronic myeloid leukemia: Overriding imatinib resistance with the Plk1 inhibitor BI 2536
    • K.V. Gleixner, V. Ferenc, B. Peter, A. Gruze, R.A. Meyer, and E. Hadzijusufovic Polo-like kinase 1 (Plk1) as a novel drug target in chronic myeloid leukemia: overriding imatinib resistance with the Plk1 inhibitor BI 2536 Cancer Res 70 2010 1513 1523
    • (2010) Cancer Res , vol.70 , pp. 1513-1523
    • Gleixner, K.V.1    Ferenc, V.2    Peter, B.3    Gruze, A.4    Meyer, R.A.5    Hadzijusufovic, E.6
  • 13
    • 84872519414 scopus 로고    scopus 로고
    • Polo-like kinase 1: A potential therapeutic option in combination with conventional chemotherapy for the management of patients with triple-negative breast cancer
    • V. Maire, F. Nemati, M. Richardson, A. Vincent-Salomon, B. Tesson, and G. Rigaill Polo-like kinase 1: a potential therapeutic option in combination with conventional chemotherapy for the management of patients with triple-negative breast cancer Cancer Res 73 2013 813 823
    • (2013) Cancer Res , vol.73 , pp. 813-823
    • Maire, V.1    Nemati, F.2    Richardson, M.3    Vincent-Salomon, A.4    Tesson, B.5    Rigaill, G.6
  • 15
    • 79951955579 scopus 로고    scopus 로고
    • The Polo-like kinase inhibitor BI 2536 exhibits potent activity against malignant plasma cells and represents a novel therapy in multiple myeloma
    • H.J. Stewart, L. Kishikova, F.L. Powell, S.P. Wheatley, and T.J. Chevassut The Polo-like kinase inhibitor BI 2536 exhibits potent activity against malignant plasma cells and represents a novel therapy in multiple myeloma Exp Hematol 39 2011 330 338
    • (2011) Exp Hematol , vol.39 , pp. 330-338
    • Stewart, H.J.1    Kishikova, L.2    Powell, F.L.3    Wheatley, S.P.4    Chevassut, T.J.5
  • 16
    • 79955068894 scopus 로고    scopus 로고
    • Inhibition of Polo-like kinase 1 leads to the suppression of osteosarcoma cell growth in vitro and in vivo
    • X. Liu, E. Choy, D. Harmon, S. Yang, C. Yang, and H. Mankin Inhibition of Polo-like kinase 1 leads to the suppression of osteosarcoma cell growth in vitro and in vivo Anticancer Drugs 22 2011 444 453
    • (2011) Anticancer Drugs , vol.22 , pp. 444-453
    • Liu, X.1    Choy, E.2    Harmon, D.3    Yang, S.4    Yang, C.5    Mankin, H.6
  • 19
    • 84857680603 scopus 로고    scopus 로고
    • Polo-like kinase 1 (PLK1) inhibition suppresses cell growth and enhances radiation sensitivity in medulloblastoma cells
    • P.S. Harris, S. Venkataraman, I. Alimova, D.K. Birks, A.M. Donson, and J. Knipstein Polo-like kinase 1 (PLK1) inhibition suppresses cell growth and enhances radiation sensitivity in medulloblastoma cells BMC Cancer 12 2012 80
    • (2012) BMC Cancer , vol.12 , pp. 80
    • Harris, P.S.1    Venkataraman, S.2    Alimova, I.3    Birks, D.K.4    Donson, A.M.5    Knipstein, J.6
  • 20
    • 33749010621 scopus 로고    scopus 로고
    • A phase I pharmacokinetic study of HMN-214, a novel oral stilbene derivative with polo-like kinase-1-interacting properties, in patients with advanced solid tumors
    • DOI 10.1158/1078-0432.CCR-06-0214
    • L.L. Garland, C. Taylor, D.L. Pilkington, J.L. Cohen, and D.D. Von Hoff A phase I pharmacokinetic study of HMN-214, a novel oral stilbene derivative with Polo-like kinase-1-interacting properties, in patients with advanced solid tumors Clin Cancer Res 12 2006 5182 5189 (Pubitemid 44453347)
    • (2006) Clinical Cancer Research , vol.12 , Issue.17 , pp. 5182-5189
    • Garland, L.L.1    Taylor, C.2    Pilkington, D.L.3    Cohen, J.L.4    Von Hoff, D.D.5
  • 21
    • 57149119488 scopus 로고    scopus 로고
    • Phase i study of on 01910.Na, a novel modulator of the Polo-like kinase 1 pathway, in adult patients with solid tumors
    • A. Jimeno, J. Li, W.A. Messersmith, D. Laheru, M.A. Rudek, and M. Maniar Phase I study of ON 01910.Na, a novel modulator of the Polo-like kinase 1 pathway, in adult patients with solid tumors J Clin Oncol 26 2008 5504 5510
    • (2008) J Clin Oncol , vol.26 , pp. 5504-5510
    • Jimeno, A.1    Li, J.2    Messersmith, W.A.3    Laheru, D.4    Rudek, M.A.5    Maniar, M.6
  • 22
    • 79956014825 scopus 로고    scopus 로고
    • Phase i study of GSK461364, a specific and competitive Polo-like kinase 1 inhibitor, in patients with advanced solid malignancies
    • D. Olmos, D. Barker, R. Sharma, A.T. Brunetto, T.A. Yap, and A.B. Taegtmeyer Phase I study of GSK461364, a specific and competitive Polo-like kinase 1 inhibitor, in patients with advanced solid malignancies Clin Cancer Res 17 2011 3420 3430
    • (2011) Clin Cancer Res , vol.17 , pp. 3420-3430
    • Olmos, D.1    Barker, D.2    Sharma, R.3    Brunetto, A.T.4    Yap, T.A.5    Taegtmeyer, A.B.6
  • 23
    • 33846931644 scopus 로고    scopus 로고
    • The small-molecule inhibitor BI 2536 reveals novel insights into mitotic roles of Polo-like kinase 1
    • P. Lenart, M. Petronczki, M. Steegmaier, B. Di Fiore, J.J. Lipp, and M. Hoffmann The small-molecule inhibitor BI 2536 reveals novel insights into mitotic roles of Polo-like kinase 1 Curr Biol 17 2007 304 315
    • (2007) Curr Biol , vol.17 , pp. 304-315
    • Lenart, P.1    Petronczki, M.2    Steegmaier, M.3    Di Fiore, B.4    Lipp, J.J.5    Hoffmann, M.6
  • 25
    • 84861681511 scopus 로고    scopus 로고
    • Reduced efficacy of the Plk1 inhibitor BI 2536 on the progression of hepatocellular carcinoma due to low intratumoral drug levels
    • J. Haupenthal, V. Bihrer, H. Korkusuz, O. Kollmar, C. Schmithals, and S. Kriener Reduced efficacy of the Plk1 inhibitor BI 2536 on the progression of hepatocellular carcinoma due to low intratumoral drug levels Neoplasia 14 2012 410 419
    • (2012) Neoplasia , vol.14 , pp. 410-419
    • Haupenthal, J.1    Bihrer, V.2    Korkusuz, H.3    Kollmar, O.4    Schmithals, C.5    Kriener, S.6
  • 26
    • 73949135792 scopus 로고    scopus 로고
    • Mechanisms of multidrug resistance in cancer
    • J.P. Gillet, and M.M. Gottesman Mechanisms of multidrug resistance in cancer Methods Mol Biol 596 2010 47 76
    • (2010) Methods Mol Biol , vol.596 , pp. 47-76
    • Gillet, J.P.1    Gottesman, M.M.2
  • 27
    • 82955229539 scopus 로고    scopus 로고
    • The emergence of drug transporter-mediated multidrug resistance to cancer chemotherapy
    • C.P. Wu, C.H. Hsieh, and Y.S. Wu The emergence of drug transporter-mediated multidrug resistance to cancer chemotherapy Mol Pharm 8 2011 1996 2011
    • (2011) Mol Pharm , vol.8 , pp. 1996-2011
    • Wu, C.P.1    Hsieh, C.H.2    Wu, Y.S.3
  • 28
    • 79961072419 scopus 로고    scopus 로고
    • Synthesis and characterization of a BODIPY conjugate of the BCR-ABL kinase inhibitor Tasigna (nilotinib): Evidence for transport of Tasigna and its fluorescent derivative by ABC drug transporters
    • S. Shukla, A.P. Skoumbourdis, M.J. Walsh, A.M. Hartz, K.L. Fung, and C.P. Wu Synthesis and characterization of a BODIPY conjugate of the BCR-ABL kinase inhibitor Tasigna (nilotinib): evidence for transport of Tasigna and its fluorescent derivative by ABC drug transporters Mol Pharm 8 2011 1292 1302
    • (2011) Mol Pharm , vol.8 , pp. 1292-1302
    • Shukla, S.1    Skoumbourdis, A.P.2    Walsh, M.J.3    Hartz, A.M.4    Fung, K.L.5    Wu, C.P.6
  • 29
    • 84872679733 scopus 로고    scopus 로고
    • Overexpression of ATP-binding cassette transporter ABCG2 as a potential mechanism of acquired resistance to vemurafenib in BRAF(V600E) mutant cancer cells
    • C.P. Wu, H.M. Sim, Y.H. Huang, Y.C. Liu, S.H. Hsiao, and H.W. Cheng Overexpression of ATP-binding cassette transporter ABCG2 as a potential mechanism of acquired resistance to vemurafenib in BRAF(V600E) mutant cancer cells Biochem Pharmacol 85 2013 325 334
    • (2013) Biochem Pharmacol , vol.85 , pp. 325-334
    • Wu, C.P.1    Sim, H.M.2    Huang, Y.H.3    Liu, Y.C.4    Hsiao, S.H.5    Cheng, H.W.6
  • 30
    • 79955104632 scopus 로고    scopus 로고
    • Tyrosine kinase inhibitors as modulators of ATP binding cassette multidrug transporters: Substrates, chemosensitizers or inducers of acquired multidrug resistance
    • A. Brozik, C. Hegedus, Z. Erdei, T. Hegedus, C. Ozvegy-Laczka, and G. Szakacs Tyrosine kinase inhibitors as modulators of ATP binding cassette multidrug transporters: substrates, chemosensitizers or inducers of acquired multidrug resistance Expert Opin Drug Metab Toxicol 7 2011 623 642
    • (2011) Expert Opin Drug Metab Toxicol , vol.7 , pp. 623-642
    • Brozik, A.1    Hegedus, C.2    Erdei, Z.3    Hegedus, T.4    Ozvegy-Laczka, C.5    Szakacs, G.6
  • 33
    • 0022457103 scopus 로고
    • Human multidrug-resistant cell lines: Increased mdr1 expression can precede gene amplification
    • D.W. Shen, A. Fojo, J.E. Chin, I.B. Roninson, N. Richert, and I. Pastan Human multidrug-resistant cell lines: increased mdr1 expression can precede gene amplification Science 232 1986 643 645 (Pubitemid 16061975)
    • (1986) Science , vol.232 , Issue.4750 , pp. 643-645
    • Shen, D.-W.1    Fojo, A.2    Chin, J.E.3
  • 34
    • 0026473238 scopus 로고
    • Identification of residues in the first cytoplasmic loop of P-glycoprotein involved in the function of chimeric human MDR1-MDR2 transporters
    • S.J. Currier, S.E. Kane, M.C. Willingham, C.O. Cardarelli, I. Pastan, and M.M. Gottesman Identification of residues in the first cytoplasmic loop of P-glycoprotein involved in the function of chimeric human MDR1-MDR2 transporters J Biol Chem 267 1992 25153 25159
    • (1992) J Biol Chem , vol.267 , pp. 25153-25159
    • Currier, S.J.1    Kane, S.E.2    Willingham, M.C.3    Cardarelli, C.O.4    Pastan, I.5    Gottesman, M.M.6
  • 35
    • 0034142125 scopus 로고    scopus 로고
    • Functional characterization of glycosylation-deficient human P- glycoprotein using a vaccinia virus expression system
    • DOI 10.1007/s002320001020
    • J.J. Gribar, M. Ramachandra, C.A. Hrycyna, S. Dey, and S.V. Ambudkar Functional characterization of glycosylation-deficient human P-glycoprotein using a vaccinia virus expression system J Membr Biol 173 2000 203 214 (Pubitemid 30100212)
    • (2000) Journal of Membrane Biology , vol.173 , Issue.3 , pp. 203-214
    • Gribar, J.J.1    Ramachandra, M.2    Hrycyna, C.A.3    Dey, S.4    Ambudkar, S.V.5
  • 36
    • 0032321894 scopus 로고    scopus 로고
    • Drug-stimulatable ATPase activity in crude membranes of human MDR1- transfected mammalian cells
    • DOI 10.1016/S0076-6879(98)92039-0
    • S.V. Ambudkar Drug-stimulatable ATPase activity in crude membranes of human MDR1-transfected mammalian cells Methods Enzymol 292 1998 504 514 (Pubitemid 29343911)
    • (1998) Methods in Enzymology , vol.292 , pp. 504-514
    • Ambudkar, S.V.1
  • 37
    • 37549027669 scopus 로고    scopus 로고
    • Evidence for dual mode of action of a thiosemicarbazone, NSC73306: A potent substrate of the multidrug resistance linked ABCG2 transporter
    • C.P. Wu, S. Shukla, A.M. Calcagno, M.D. Hall, M.M. Gottesman, and S.V. Ambudkar Evidence for dual mode of action of a thiosemicarbazone, NSC73306: a potent substrate of the multidrug resistance linked ABCG2 transporter Mol Cancer Ther 6 2007 3287 3296
    • (2007) Mol Cancer Ther , vol.6 , pp. 3287-3296
    • Wu, C.P.1    Shukla, S.2    Calcagno, A.M.3    Hall, M.D.4    Gottesman, M.M.5    Ambudkar, S.V.6
  • 38
    • 84867572279 scopus 로고    scopus 로고
    • Downregulation of mdr1 and abcg2 genes is a mechanism of inhibition of efflux pumps mediated by polymeric amphiphiles
    • M.L. Cuestas, A.I. Castillo, A. Sosnik, and V.L. Mathet Downregulation of mdr1 and abcg2 genes is a mechanism of inhibition of efflux pumps mediated by polymeric amphiphiles Bioorg Med Chem Lett 22 2012 6577 6579
    • (2012) Bioorg Med Chem Lett , vol.22 , pp. 6577-6579
    • Cuestas, M.L.1    Castillo, A.I.2    Sosnik, A.3    Mathet, V.L.4
  • 40
    • 84872675468 scopus 로고    scopus 로고
    • The Pim kinase inhibitor SGI-1776 decreases cell surface expression of P-glycoprotein (ABCB1) and breast cancer resistance protein (ABCG2) and drug transport by Pim-1-dependent and -independent mechanisms
    • K. Natarajan, J. Bhullar, S. Shukla, M. Burcu, Z.S. Chen, and S.V. Ambudkar The Pim kinase inhibitor SGI-1776 decreases cell surface expression of P-glycoprotein (ABCB1) and breast cancer resistance protein (ABCG2) and drug transport by Pim-1-dependent and -independent mechanisms Biochem Pharmacol 85 2013 514 524
    • (2013) Biochem Pharmacol , vol.85 , pp. 514-524
    • Natarajan, K.1    Bhullar, J.2    Shukla, S.3    Burcu, M.4    Chen, Z.S.5    Ambudkar, S.V.6
  • 41
    • 54249157033 scopus 로고    scopus 로고
    • Lapatinib (Tykerb, GW572016) reverses multidrug resistance in cancer cells by inhibiting the activity of ATP-binding cassette subfamily B member 1 and G member 2
    • C.L. Dai, A.K. Tiwari, C.P. Wu, X.D. Su, S.R. Wang, and D.G. Liu Lapatinib (Tykerb, GW572016) reverses multidrug resistance in cancer cells by inhibiting the activity of ATP-binding cassette subfamily B member 1 and G member 2 Cancer Res 68 2008 7905 7914
    • (2008) Cancer Res , vol.68 , pp. 7905-7914
    • Dai, C.L.1    Tiwari, A.K.2    Wu, C.P.3    Su, X.D.4    Wang, S.R.5    Liu, D.G.6
  • 42
    • 84862811607 scopus 로고    scopus 로고
    • Tyrosine kinase inhibitors as modulators of ABC transporter-mediated drug resistance
    • S. Shukla, Z.S. Chen, and S.V. Ambudkar Tyrosine kinase inhibitors as modulators of ABC transporter-mediated drug resistance Drug Resist Updat 15 2012 70 80
    • (2012) Drug Resist Updat , vol.15 , pp. 70-80
    • Shukla, S.1    Chen, Z.S.2    Ambudkar, S.V.3
  • 43
    • 13244271313 scopus 로고    scopus 로고
    • Polo-like kinases (Plks) and cancer
    • DOI 10.1038/sj.onc.1208272
    • N. Takai, R. Hamanaka, J. Yoshimatsu, and I. Miyakawa Polo-like kinases (Plks) and cancer Oncogene 24 2005 287 291 (Pubitemid 40188609)
    • (2005) Oncogene , vol.24 , Issue.2 , pp. 287-291
    • Takai, N.1    Hamanaka, R.2    Yoshimatsu, J.3    Miyakawa, I.4
  • 44
    • 84876055711 scopus 로고    scopus 로고
    • Screening compounds with a novel high-throughput ABCB1-mediated efflux assay identifies drugs with known therapeutic targets at risk for multidrug resistance interference
    • M.R. Ansbro, S. Shukla, S.V. Ambudkar, S.H. Yuspa, and L. Li Screening compounds with a novel high-throughput ABCB1-mediated efflux assay identifies drugs with known therapeutic targets at risk for multidrug resistance interference PLoS One 8 2013 e60334
    • (2013) PLoS One , vol.8 , pp. 60334
    • Ansbro, M.R.1    Shukla, S.2    Ambudkar, S.V.3    Yuspa, S.H.4    Li, L.5
  • 45
    • 0030868612 scopus 로고    scopus 로고
    • Relation between the turnover number for vinblastine transport and for vinblastine-stimulated ATP hydrolysis by human P-glycoprotein
    • DOI 10.1074/jbc.272.34.21160
    • S.V. Ambudkar, C.O. Cardarelli, I. Pashinsky, and W.D. Stein Relation between the turnover number for vinblastine transport and for vinblastine-stimulated ATP hydrolysis by human P-glycoprotein J Biol Chem 272 1997 21160 21166 (Pubitemid 27373976)
    • (1997) Journal of Biological Chemistry , vol.272 , Issue.34 , pp. 21160-21166
    • Ambudkar, S.V.1    Cardarelli, C.O.2    Pashinsky, I.3    Stein, W.D.4
  • 46
    • 33646424730 scopus 로고    scopus 로고
    • Selective toxicity of NSC73306 in MDR1-positive cells as a new strategy to circumvent multidrug resistance in cancer
    • J.A. Ludwig, G. Szakacs, S.E. Martin, B.F. Chu, C. Cardarelli, and Z.E. Sauna Selective toxicity of NSC73306 in MDR1-positive cells as a new strategy to circumvent multidrug resistance in cancer Cancer Res 66 2006 4808 4815
    • (2006) Cancer Res , vol.66 , pp. 4808-4815
    • Ludwig, J.A.1    Szakacs, G.2    Martin, S.E.3    Chu, B.F.4    Cardarelli, C.5    Sauna, Z.E.6
  • 47
    • 79953324568 scopus 로고    scopus 로고
    • Improving cancer chemotherapy with modulators of ABC drug transporters
    • S. Shukla, S. Ohnuma, and S.V. Ambudkar Improving cancer chemotherapy with modulators of ABC drug transporters Curr Drug Targets 12 2011 621 630
    • (2011) Curr Drug Targets , vol.12 , pp. 621-630
    • Shukla, S.1    Ohnuma, S.2    Ambudkar, S.V.3


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