ACTINOMYCIN-D CAUSES MULTIDRUG-RESISTANCE AND DIFFERENTIATION IN A HUMAN RHABDOMYOSARCOMA CELL-LINE

被引:0
作者
MELGUIZO, C
PRADOS, J
FERNANDEZ, JE
VELEZ, C
ALVAREZ, L
ARANEGA, A
机构
关键词
RHABDOMYOSARCOMA; MULTIDRUG RESISTANCE; ACTINOMYCIN-D; P-GLYCOPROTEIN; CELL DIFFERENTIATION;
D O I
暂无
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 emergence of drug-resistant tumor cells remains a major problem in cancer chemotherapy. Resistance to multiple unrelated antineoplastic drugs may be related, in part, to expression of the P-glycoprotein. The cell line RD, derived from an embryonic rhabdomyosarcoma tumor, was used as an in vitro model to examine the development of drug resistance. A cell line resistant to actinomycin D (RD-DAC) was developed by growing RD in increasing concentrations of the drug. The ID50 (concentration of drug needed to induce a 50% reduction in cell growth) of the resultant line to actinomycin D was more than 15 times that of the parental line. The resistant line was cross-resistant to vincristine and doxorubicin. Resistance to actinomycin D resulted in increased P-glycoprotein expression, which was associated with a change in desmin and vimentin expression. These results suggest that exposure to chemotherapeutic drugs can induce not only classical multidrug resistance, but also a process of cellular differentiation in rhabdomyosarcoma cells.
引用
收藏
页码:137 / 145
页数:9
相关论文
共 43 条
[41]  
WHITE L, 1989, CANCER, V63, P2103, DOI 10.1002/1097-0142(19890601)63:11<2103::AID-CNCR2820631106>3.0.CO
[42]  
2-N
[43]  
YU FL, 1990, BIOCHEM INT, V20, P807