MULTIDRUG-RESISTANCE IN CANCER-CHEMOTHERAPY

被引:66
作者
PATEL, NH
ROTHENBERG, ML
机构
[1] UNIV TEXAS,HLTH SCI CTR,DIV ONCOL,SAN ANTONIO,TX 78284
[2] UNIV TEXAS,HLTH SCI CTR,CLIN PHARM PROGRAM,SAN ANTONIO,TX 78284
关键词
MULTIDRUG RESISTANCE; P-GLYCOPROTEIN; CHEMOTHERAPY;
D O I
10.1007/BF00873229
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Resistance to chemotherapy is the single most important reason for treatment failure in cancer patients. Over the past 15 years, we have gained significant insight into one of the mechanisms responsible for this process: multidrug resistance (MDR). Far from being a phenomenon limited to the laboratory, multidrug resistance has been identified in a wide variety of newly diagnosed and recurrent human tumors. A number of compounds can block p-glycoprotein and overcome MDR in vitro and in vivo. Current strategies to block MDR are discussed in this review. Future research in this area will focus on the identification of more selective and potent MDR reversing agents and the development of entirely new approaches to overcoming multidrug resistance such as monoclonal antibodies, immunotoxins, and gene therapy.
引用
收藏
页码:1 / 13
页数:13
相关论文
共 103 条
[51]  
KELLEN JA, 1991, ANTICANCER RES, V11, P1243
[52]  
KESSEL D, 1968, CANCER RES, V28, P938
[53]   THE DIRECT ACTIVATION OF HUMAN MULTIDRUG RESISTANCE GENE (MDR1) BY ANTICANCER AGENTS [J].
KOHNO, K ;
SATO, S ;
TAKANO, H ;
MATSUO, K ;
KUWANO, M .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1989, 165 (03) :1415-1421
[54]  
KUWAZURU Y, 1990, BLOOD, V76, P2065
[55]  
LENHERT M, 1991, BLOOD, V77, P348
[56]  
LING V, 1992, CANCER-AM CANCER SOC, V69, P2603, DOI 10.1002/1097-0142(19920515)69:10<2603::AID-CNCR2820691034>3.0.CO
[57]  
2-E
[58]   PHASE-I/II TRIAL OF CYCLOSPORINE AS A CHEMOTHERAPY-RESISTANCE MODIFIER IN ACUTE-LEUKEMIA [J].
LIST, AF ;
SPIER, C ;
GREER, J ;
WOLFF, S ;
HUTTER, J ;
DORR, R ;
SALMON, S ;
FUTSCHER, B ;
BAIER, M ;
DALTON, W .
JOURNAL OF CLINICAL ONCOLOGY, 1993, 11 (09) :1652-1660
[59]  
LIZARD G, 1992, EUR UROL S1, V2, P39
[60]   ALTERATION OF ETOPOSIDE PHARMACOKINETICS AND PHARMACODYNAMICS BY CYCLOSPORINE IN A PHASE-I TRIAL TO MODULATE MULTIDRUG RESISTANCE [J].
LUM, BL ;
KAUBISCH, S ;
YAHANDA, AM ;
ADLER, KM ;
JEW, L ;
EHSAN, MN ;
BROPHY, NA ;
HALSEY, J ;
GOSLAND, MP ;
SIKIC, BI .
JOURNAL OF CLINICAL ONCOLOGY, 1992, 10 (10) :1635-1642