Nucleoside transport and its significance for anticancer drug resistance

被引:132
作者
Mackey, JR
Baldwin, SA
Young, JD
Cass, CE
机构
[1] Univ Alberta, Dept Oncol, Edmonton, AB T6G 1Z2, Canada
[2] Cross Canc Inst, Edmonton, AB T6G 1Z2, Canada
[3] Univ Leeds, Sch Biochem & Mol Biol, Leeds LS2 9JT, W Yorkshire, England
[4] Univ Alberta, Dept Physiol, Edmonton, AB T6G 1Z2, Canada
基金
英国医学研究理事会; 英国惠康基金;
关键词
D O I
10.1016/S1368-7646(98)80047-2
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
This article discusses the role of nucleoside transport processes in the cytotoxicity of clinically important anticancer nucleosides. This article summarizes recent advances in the molecular biology of nucleoside transport proteins, review the current state of knowledge of the transportability of therapeutically useful anticancer nucleosides, and provide an overview of the role of nucleoside transport deficiency as a mechanism of resistance to nucleoside cytotoxicity are summarized. Several strategies for utilization of nucleoside transport processes to improve the therapeutic index of anticancer therapies, including the use of nucleoside-transport inhibitors to modulate toxicity of both nucleoside and nonnucleoside antimetabolite drugs are also presented.
引用
收藏
页码:310 / 324
页数:15
相关论文
共 128 条
[1]   PROTECTION AGAINST FLUDARABINE NEUROTOXICITY IN LEUKEMIC MICE BY THE NUCLEOSIDE TRANSPORT INHIBITOR NITROBENZYLTHIOINOSINE [J].
ADJEI, AA ;
DAGNINO, L ;
WONG, MMY ;
PATERSON, ARP .
CANCER CHEMOTHERAPY AND PHARMACOLOGY, 1992, 31 (01) :71-75
[2]  
ALESSISEVERINI S, 1995, LEUKEMIA, V9, P1674
[3]   Sensitization of hematopoietic stem and progenitor cells to trimetrexate using nucleoside transport inhibitors [J].
Allay, JA ;
Spencer, HT ;
Wilkinson, SL ;
Belt, JA ;
Blakley, RL ;
Sorrentino, BP .
BLOOD, 1997, 90 (09) :3546-3554
[4]  
ALLEGRA CJ, 1997, CANC PRINCIPLES PRAC, V1, P490
[5]   Nucleoside transport inhibition by draflazine in unstable coronary disease [J].
Andersen, K ;
Dellborg, M ;
Swedberg, K .
EUROPEAN JOURNAL OF CLINICAL PHARMACOLOGY, 1996, 51 (01) :7-13
[6]  
ARONOW B, 1985, J BIOL CHEM, V260, P6274
[7]  
AVERY TL, 1989, CANCER RES, V49, P4972
[8]  
AVRAMIS VI, 1982, CANCER RES, V42, P2587
[9]   A PHASE-I TRIAL OF 5-FLUOROURACIL, LEUCOVORIN, AND DIPYRIDAMOLE GIVEN BY CONCURRENT 120-H CONTINUOUS INFUSIONS [J].
BAILEY, H ;
WILDING, G ;
TUTSCH, KD ;
ARZOOMANIAN, RZ ;
ALBERTI, D ;
TOMBES, MB ;
GREM, JL ;
SPRIGGS, DR .
CANCER CHEMOTHERAPY AND PHARMACOLOGY, 1992, 30 (04) :297-302
[10]   2'-DEOXY-2'-METHYLENECYTIDINE AND 2'-DEOXY-2',2'-DIFLUOROCYTIDINE 5'-DIPHOSPHATES - POTENT MECHANISM-BASED INHIBITORS OF RIBONUCLEOTIDE REDUCTASE [J].
BAKER, CH ;
BANZON, J ;
BOLLINGER, JM ;
STUBBE, J ;
SAMANO, V ;
ROBINS, MJ ;
LIPPERT, B ;
JARVI, E ;
RESVICK, R .
JOURNAL OF MEDICINAL CHEMISTRY, 1991, 34 (06) :1879-1884