Biochemical, cellular, and pharmacological aspects of the multidrug transporter

被引:1773
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.
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页码:361 / 398
页数:38
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