Biochemical, cellular, and pharmacological aspects of the multidrug transporter

被引:1789
作者
Ambudkar, SV [1 ]
Dey, S
Hrycyna, CA
Ramachandra, M
Pastan, I
Gottesman, MM
机构
[1] NCI, Cell Biol Lab, Div Basic Sci, NIH, Bethesda, MD 20892 USA
[2] NCI, Mol Biol Lab, Div Basic Sci, NIH, Bethesda, MD 20892 USA
关键词
multidrug resistance; P-glycoprotein; drug transport; ATP hydrolysis; cancer chemotherapy; chemosensitizer;
D O I
10.1146/annurev.pharmtox.39.1.361
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Considerable evidence has accumulated indicating that the multidrug transporter or P-glycoprotein plays a role in the development of simultaneous resistance to multiple cytotoxic drugs in cancer cells. In recent years, various approaches such as mutational analyses and biochemical and pharmacological characterization have yielded significant information about the relationship of structure and function of P-glycoprotein. However, there is still considerable controversy about the mechanism of action of this efflux pump and its function in normal cells. This review summarizes current research on the structure-function analysis of P-glycoprotein, its mechanism of action, and facts and speculations about ifs normal physiological role.
引用
收藏
页码:361 / 398
页数:38
相关论文
共 169 条
[41]   Functional reconstitution of P-glycoprotein reveals an apparent near stoichiometric drug transport to ATP hydrolysis [J].
Eytan, GD ;
Regev, R ;
Assaraf, YG .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (06) :3172-3178
[42]   Experimental reversal of P-glycoprotein-mediated multidrug resistance by pharmacological chemosensitisers [J].
Ford, JM .
EUROPEAN JOURNAL OF CANCER, 1996, 32A (06) :991-1001
[43]  
FORD JM, 1990, PHARMACOL REV, V42, P155
[44]  
FORD JM, 1990, CANCER RES, V50, P1748
[45]  
FORD JM, 1989, MOL PHARMACOL, V35, P105
[46]   EXPRESSION OF A HUMAN MULTIDRUG RESISTANCE CDNA (MDR1) IN THE BONE-MARROW OF TRANSGENIC MICE - RESISTANCE TO DAUNOMYCIN-INDUCED LEUKOPENIA [J].
GALSKI, H ;
SULLIVAN, M ;
WILLINGHAM, MC ;
CHIN, KV ;
GOTTESMAN, MM ;
PASTAN, I ;
MERLINO, GT .
MOLECULAR AND CELLULAR BIOLOGY, 1989, 9 (10) :4357-4363
[47]   KT-5720 REVERSES MULTIDRUG-RESISTANCE IN VARIANT S49 MOUSE LYMPHOMA-CELLS TRANSDUCED WITH THE HUMAN MDR1 CDNA AND IN HUMAN MULTIDRUG-RESISTANT CARCINOMA-CELLS [J].
GALSKI, H ;
LAZAROVICI, P ;
GOTTESMAN, MM ;
MURAKATA, C ;
MATSUDA, Y ;
HOCHMAN, J .
EUROPEAN JOURNAL OF CANCER, 1995, 31A (03) :380-388
[48]   Competitive and non-competitive inhibition of the multidrug-resistance-associated P-glycoprotein ATPase - Further experimental evidence for a multisite model [J].
Garrigos, M ;
Mir, LM ;
Orlowski, S .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1997, 244 (02) :664-673
[49]   P-glycoprotein - A mediator of multidrug resistance in tumour cells [J].
Germann, UA .
EUROPEAN JOURNAL OF CANCER, 1996, 32A (06) :927-944
[50]   Characterization of phosphorylation-defective mutants of human P-glycoprotein expressed in mammalian cells [J].
Germann, UA ;
Chambers, TC ;
Ambudkar, SV ;
Licht, T ;
Cardarelli, CO ;
Pastan, I ;
Gottesman, MM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (03) :1708-1716