A critical evaluation of the mechanisms of action proposed for the antitumor effects of the anthracycline antibiotics Adriamycin and daunorubicin

被引:1815
作者
Gewirtz, DA [1 ]
机构
[1] Virginia Commonwealth Univ, Med Coll Virginia, Dept Pharmacol Toxicol & Med, Richmond, VA 23298 USA
关键词
Adriamycin (doxorubicin); daunomycin (daunorubicin); free radical mechanisms; inhibition of topoisomerase II; DNA biosynthesis;
D O I
10.1016/S0006-2952(98)00307-4
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The mechanisms responsible for the antiproliferative and cytotoxic effects of the anthracycline antibiotics doxorubicin (Adriamycin(R)) and daunorubicin (daunomycin) have been the subject of considerable controversy. This commentary addresses the potential role of DNA synthesis inhibition, free radical formation and lipid peroxidation, DNA binding and alkylation, DNA cross-linking, interference with DNA strand separation and helicase activity, direct membrane effects, and the initiation of DNA damage via the inhibition of topoisomerase II in the interaction of these drugs with the tumor cell. One premise underlying this analysis is that only studies utilizing drug concentrations that reflect the plasma levels in the patient after either bolus administration or continuous infusion are considered to reflect the basis for drug action in the clinic. The role of free radicals in anthracycline cardiotoxicity is also discussed. (C) 1999 Elsevier Science Inc.
引用
收藏
页码:727 / 741
页数:15
相关论文
共 199 条
[1]  
ABDELLA BRJ, 1995, ENV HLTH PERSPECT, V64, P3
[2]  
[Anonymous], CANC CHEMOTHERAPY BI
[3]   PROTECTIVE ROLE OF THE GLUTATHIONE REDOX CYCLE AGAINST ADRIAMYCIN-MEDIATED TOXICITY IN ISOLATED HEPATOCYTES [J].
BABSON, JR ;
ABELL, NS ;
REED, DJ .
BIOCHEMICAL PHARMACOLOGY, 1981, 30 (16) :2299-2304
[4]   Anthracycline antibiotic blockade of SV40 T antigen helicase action [J].
Bachur, NR ;
Lun, L ;
Sun, PM ;
Trubey, CM ;
Elliott, EE ;
Egorin, MJ ;
Malkas, L ;
Hickey, R .
BIOCHEMICAL PHARMACOLOGY, 1998, 55 (07) :1025-1034
[5]  
BACHUR NR, 1992, MOL PHARMACOL, V41, P993
[6]  
BACHUR NR, 1977, MOL PHARMACOL, V13, P901
[7]  
BACHUR NR, 1978, CANCER RES, V38, P1745
[8]  
BACHUR NR, 1993, MOL PHARMACOL, V44, P1064
[9]   LIPID-PEROXIDATION, PHOSPHOINOSITIDE TURNOVER AND PROTEIN-KINASE-C ACTIVATION IN HUMAN PLATELETS TREATED WITH ANTHRACYCLINES AND THEIR COMPLEXES WITH FE(III) [J].
BANFI, P ;
PAROLINI, O ;
LANZI, C ;
GAMBETTA, RA .
BIOCHEMICAL PHARMACOLOGY, 1992, 43 (07) :1521-1527
[10]   DEOXYRIBOSE BREAKDOWN BY THE ADRIAMYCIN SEMI-QUINONE AND H2O2 - EVIDENCE FOR HYDROXYL RADICAL PARTICIPATION [J].
BATES, DA ;
WINTERBOURN, CC .
FEBS LETTERS, 1982, 145 (01) :137-142