Resistance to 5-fluorouracil

被引:96
|
作者
Mader, RM
Müller, M
Steger, GG
机构
[1] Univ Vienna, Sch Med, Dept Internal Med 1, Div Oncol, A-1090 Vienna, Austria
[2] Univ Vienna, Sch Med, Dept Clin Pharmacol, Div Oncol, A-1090 Vienna, Austria
来源
GENERAL PHARMACOLOGY | 1998年 / 31卷 / 05期
关键词
5-fluorouracil; resistance; metabolism RNA processing; apoptosis;
D O I
10.1016/S0306-3623(98)00191-8
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
1. Primary and secondary resistance to the widely used antimetabolite 5-fluorouracil (5-FU) are common phenomena in cancer chemotherapy. Because 5 FU still remains the agent of choice in the treatment of, for example, colorectal cancer, circumvention of resistance is of vital importance. 2. Resistance to fluoropyrimidines is a multifactorial event, which includes transport mechanisms, metabolism, molecular mechanisms, protection from apoptosis, and resistance via cell cycle kinetics. To date, the prediction of primary resistance to 5-FU in the clinic is limited to few studies focusing mainly on the key enzyme thymidylate synthase. To gain a deeper insight into the key events responsible for 5-FU resistance in vivo, the evaluation of additional parameters such as other (fluoro)pyrimidine converting enzymes, the mutational status of regulators of apoptosis, and tumour angiogenesis is currently under investigation. 3. Most studies on the circumvention of fluoropyrimidine resistance refer to preclinical investigations and were rarely confirmed in clinical trials. Although our understanding of resistance to 5-FU leaves many open questions, the fundamental insights accomplished during the last years provide a rational understanding to exceed the bounds of the actual therapeutic schedules. (C) 1998 Elsevier Science Inc.
引用
收藏
页码:661 / 666
页数:6
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