Pharmacokinetic resistance to imatinib mesylate - Role of the ABC drug pumps ABCG2 (BCRP) and ABCB1 (MDR1) in the oral bioavailability of imatinib

被引:91
作者
Burger, H [1 ]
Nooter, K [1 ]
机构
[1] Erasmus MC, Josephine Nefkens Inst, Dept Med Oncol, NL-3000 DR Rotterdam, Netherlands
关键词
imatinib mesylate; pharmacokinetic resistance; gleevec; oral bioavailability; ABC transporters; caco-2; cells;
D O I
10.4161/cc.3.12.1331
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Imatinib mesylate is a selective tyrosine kinase inhibitor that is successfully used in the treatment of chronic myeloid leukaemias and gastrointestinal stromal tumours. The drug is taken orally on a daily basis in order to suppress tumour growth. Unfortunately, the vast majority of patients will eventually progress while on therapy. It is generally thought that this acquired unresponsiveness is due to gene amplification or somatic mutations in the drug's target genes. However, we have now evidence, based on several in vitro and in vivo observations suggesting that pharmacokinetic resistance may also play a definitive role in the ultimate resistance of patients on chronic imatinib. Our findings may have serious implications for the chronic imatinib treatment of cancer patients.
引用
收藏
页码:1502 / 1505
页数:4
相关论文
共 28 条
  • [1] Buchdunger E, 2000, J PHARMACOL EXP THER, V295, P139
  • [2] Imatinib mesylate (STI571) is a substrate for the breast cancer resistance protein (BCRP)/ABCG2 drug pump
    Burger, H
    van Tol, H
    Boersma, AWM
    Brok, M
    Wiemer, EAC
    Stoler, G
    Nooter, K
    [J]. BLOOD, 2004, 104 (09) : 2940 - 2942
  • [3] A missense mutation in KIT kinase domain 1 correlates with imatinib resistance in gastrointestinal stromal tumors
    Chen, LL
    Trent, JC
    Wu, EF
    Fuller, GN
    Ramdas, L
    Zhang, W
    Raymond, AK
    Prieto, VG
    Oyedeji, CO
    Hunt, KK
    Pollock, RE
    Feig, BW
    Hayes, KJ
    Choi, H
    Macapinlac, HA
    Hittelman, W
    Velasco, MA
    Patel, S
    Burgess, MA
    Benjamin, RS
    Frazier, ML
    [J]. CANCER RESEARCH, 2004, 64 (17) : 5913 - 5919
  • [4] EXPRESSION OF THE MULTIDRUG RESISTANCE GENE-PRODUCT (P-GLYCOPROTEIN) IN HUMAN NORMAL AND TUMOR-TISSUES
    CORDONCARDO, C
    OBRIEN, JP
    BOCCIA, J
    CASALS, D
    BERTINO, JR
    MELAMED, MR
    [J]. JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 1990, 38 (09) : 1277 - 1287
  • [5] Distribution of STI-571 to the brain is limited by P-glycoprotein-mediated efflux
    Dai, HQ
    Marbach, P
    Lemaire, M
    Hayes, M
    Elmquist, WF
    [J]. JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2003, 304 (03) : 1085 - 1092
  • [6] Use of c-KIT/PDGFRA mutational analysis to predict the clinical response to imatinib in patients with advanced gastrointestinal stromal tumours entered on phase I and II studies of the EORTC Soft Tissue and Bone Sarcoma Group
    Debiec-Rychter, M
    Dumez, H
    Judson, I
    Wasag, B
    Verweij, J
    Brown, M
    Dimitrijevic, S
    Sciot, R
    Stul, M
    Vranck, H
    Scurr, M
    Hagemeijer, A
    Van Glabbeke, M
    van Oosterom, AT
    [J]. EUROPEAN JOURNAL OF CANCER, 2004, 40 (05) : 689 - 695
  • [7] Efficacy and safety of imatinib mesylate in advanced gastrointestinal stromal tumors
    Demetri, GD
    von Mehren, M
    Blanke, CD
    Van den Abbeele, AD
    Eisenberg, B
    Roberts, PJ
    Heinrich, MC
    Tuveson, DA
    Singer, S
    Janicek, M
    Fletcher, JA
    Silverman, SG
    Silberman, SL
    Capdeville, R
    Kiese, B
    Peng, B
    Dimitrijevic, S
    Druker, BJ
    Corless, C
    Fletcher, CDM
    Joensuu, H
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2002, 347 (07) : 472 - 480
  • [8] Multidrug resistance mediated by the breast cancer resistance protein BCRP (ABCG2)
    Doyle, LA
    Ross, DD
    [J]. ONCOGENE, 2003, 22 (47) : 7340 - 7358
  • [9] Activity of a specific inhibitor of the BCR-ABL tyrosine kinase in the blast crisis of chronic myeloid leukemia and acute lymphoblastic leukemia with the philadelphia chromosome.
    Druker, BJ
    Sawyers, CL
    Kantarjian, H
    Resta, DJ
    Reese, SF
    Ford, JM
    Capdeville, R
    Talpaz, M
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2001, 344 (14) : 1038 - 1042
  • [10] Efficacy and safety of a specific inhibitor of the BCR-ABL tyrosine kinase in chronic myeloid leukemia.
    Druker, BJ
    Talpaz, M
    Resta, DJ
    Peng, B
    Buchdunger, E
    Ford, JM
    Lydon, NB
    Kantarjian, H
    Capdeville, R
    Ohno-Jones, S
    Sawyers, CL
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2001, 344 (14) : 1031 - 1037