P-GLYCOPROTEIN-MEDIATED MULTIDRUG RESISTANCE AND CYTOTOXIC EFFECTOR-CELLS

被引:0
作者
SAVAS, B [1 ]
COLE, SPC [1 ]
AKOGLU, TF [1 ]
PROSS, HF [1 ]
机构
[1] QUEENS UNIV,DEPT MICROBIOL & IMMUNOL,KINGSTON K7L 3N6,ONTARIO,CANADA
关键词
MULTIDRUG RESISTANCE; P-GLYCOPROTEIN; NATURAL KILLER CELLS; LYMPHOKINE-ACTIVATED KILLER CELLS; CHEMOSENSITIZERS;
D O I
暂无
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Multidrug resistance (MDR) is one of the major obstacles to successful cancer chemotherapy. MDR is a complex and multifactorial phenomenon. One important and common mechanism used by cancer cells as a defense against cytotoxic drugs is a 170-kD plasma membrane glycoprotein, P-glycoprotein (P-gp). P-gp confers resistance by actively pumping cytotoxic drugs out of cancer cells. Paradoxically, P-gp overexpression on tumor cells is frequently associated with enhanced susceptibility to lymphokine-activated killer cell activity. This enhanced susceptibility is not observed with P-gp- MDR cells, nor is susceptibility to natural killer cells increased. The physiologic, evolutionary and immunologic concepts with regard to the P-gp and the possible intervention of the function of the P-gp in cancer therapy are reviewed.
引用
收藏
页码:177 / 192
页数:16
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