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Topoisomerase I inhibitors and drug resistance
被引:14
|作者:
Parchment, RE
Pessina, A
机构:
[1] Univ Milan, Inst Microbiol, I-20133 Milan, Italy
[2] Wayne State Univ, Barbara Ann Karmanos Canc Inst, Div Hematol Oncol, Detroit, MI USA
关键词:
camptothecin;
drug resistance;
topo I inhibitors;
topoisomerase I;
D O I:
10.1023/A:1008008719699
中图分类号:
Q81 [生物工程学(生物技术)];
Q93 [微生物学];
学科分类号:
071005 ;
0836 ;
090102 ;
100705 ;
摘要:
DNA topoisomerase I is a nuclear enzyme which catalyzes the conversion of the DNA topology by introducing single-strand breaks into the DNA molecule. This enzyme represents a novel and distinct molecule target for cancer therapy by antitopoisomerase drugs belonging to the campthotecin series of antineoplastics. As many tumors can acquire resistance to drug treatment and become refractary to the chemotherapy it is very important to investigate the mechanisms involved in such a drug resistance for circumventing the phenomenon. This article describes the role of topoisomerase I in cell functions and the methods used to assess its in vitro catalytic activity. It reviews the mechanisms of cytotoxicity of the most specific antitopoisomerase I drugs by considering also the phenomenon of drug resistance. Some factors useful to drive the future perspectives in the development of new topoisomerase I inhibitors are also evidenced and discussed.
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页码:149 / 164
页数:16
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