apoptosis;
camptothecins;
cleavable complex;
DNA damage;
topoisomerase I;
D O I:
10.1517/14728222.12.10.1243
中图分类号:
R9 [药学];
学科分类号:
1007 ;
摘要:
Background: Topoisomerase I is required for DNA relaxation during critical cellular functions. The identification of camptothecins as specific enzyme inhibitors and their clinical efficacy have stimulated extensive efforts to exploit topoisomerase I as a tumor target and explain the putative mechanisms of antitumor-specific action. Objective: This review provides an overview of the recent achievements in the development of topoisomerase I inhibitors and in the explanation of the biological pathways involved in tumor response. Results/conclusion: In spite of the difficulty to identify novel topoisomerase I inhibitors with improved pharmacological properties, a growing body of evidence supports the possibility of optimizing the therapeutic profile of available agents. The explanation of defense mechanisms and the molecular determinants of tumor cell response is expected to provide a basis for the design of combination approaches for optimization of topoisomerase I inhibitors-based therapy.
机构:
Univ Lille Nord de France, Ctr Oscar Lambret, INSERM, U837, F-59020 Lille, FranceUniv Lille Nord de France, Ctr Oscar Lambret, INSERM, U837, F-59020 Lille, France
机构:
Univ Med & Dent New Jersey, Robert Wood Johnson Med Sch, Dept Mol & Cellular Pharmacol, Canc Inst New Jersey, New Brunswick, NJ 08901 USAUniv Med & Dent New Jersey, Robert Wood Johnson Med Sch, Dept Mol & Cellular Pharmacol, Canc Inst New Jersey, New Brunswick, NJ 08901 USA
Rasheed, ZA
Rubin, EH
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机构:
Univ Med & Dent New Jersey, Robert Wood Johnson Med Sch, Dept Mol & Cellular Pharmacol, Canc Inst New Jersey, New Brunswick, NJ 08901 USAUniv Med & Dent New Jersey, Robert Wood Johnson Med Sch, Dept Mol & Cellular Pharmacol, Canc Inst New Jersey, New Brunswick, NJ 08901 USA