MODULATION OF EXPRESSION OF MULTIDRUG RESISTANCE GENE (MDR-1) BY ADRIAMYCIN

被引:26
作者
KATO, S
NISHIMURA, J
YUFU, Y
IDEGUCHI, H
UMEMURA, T
NAWATA, H
机构
[1] FUKUOKA UNIV,SCH MED,MED LAB,FUKUOKA 81401,JAPAN
[2] KYUSHU UNIV,SCH HLTH SCI,DEPT MET & MAT TECHNOL,FUKUOKA 812,JAPAN
关键词
MULTIDRUG RESISTANCE; MDR-1; P-GLYCOPROTEIN; ADRIAMYCIN;
D O I
10.1016/0014-5793(92)81269-R
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The acquired resistance to various drugs in cancer is mediated by P-glycoprotein (P-gp) which is encoded by the mdr-1 gene. An increased level of mdr-1/P-gp was demonstrated after chemotherapy administered to treat cancer in humans. To clarify the direct effect of anticancer drugs on mdr-1/P-gp expression, we investigated the change in transport of adriamycin (ADR), and the expression of the mdr-1 gene and P-gp in an ADR-treated, multidrug-resistant leukemic cell line (K562/ADR500). The addition of ADR induced the over-expression of mdr-1/P-gp, which led to a transient decrease in the intracellular accumulation of ADR although the difference was not statistically significant. A maximal effect was observed after 4 h incubation, returning to the baseline level after further incubation for 12-24 h. The phosphorylation of P-gp was inversely correlated with the levels of P-gp. These observations suggest that ADR itself modulates both the expression and function of P-gp. Determination of the optimal schedule for administering adriamycin is essential to achieving the optimal effect in treating cancer.
引用
收藏
页码:175 / 178
页数:4
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