EFFECT OF CHELATING-AGENTS AND METAL-IONS ON DEGRADATION OF DNA BY BLEOMYCIN

被引:414
作者
SAUSVILLE, EA
PEISACH, J
HORWITZ, SB
机构
[1] YESHIVA UNIV,ALBERT EINSTEIN COLL MED,DEPT MOLEC PHARMACOL,BRONX,NY 10461
[2] YESHIVA UNIV,ALBERT EINSTEIN COLL MED,DEPT CELL BIOL,BRONX,NY 10461
[3] YESHIVA UNIV,ALBERT EINSTEIN COLL MED,DEPT MOLEC BIOL,BRONX,NY 10461
关键词
D O I
10.1021/bi00607a007
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The degradation of DNA by bleomycin was studied in the absence and in the presence of added reducing agents, including 2-mercaptoethanol, dithiothreitol, reduced nicotinamide adenine dinucleotide phosphate, H2O2, and ascorbate, and in the presence of a superoxide anion generating system consisting of xanthine oxidase and hypoxanthine. In all cases, breakage of DNA was inhibited by low concentrations of chelators; where examined in detail, deferoxamine mesylate was considerably more potent than (ethylenedinitrilo)tetraacetic acid. Iron was found to be present in significant quantities in all reaction mixtures. Thus, the pattern of inhibition observed is attributed to the involvement of contaminating iron in the degradation of DNA by bleomycin. Cu(II), Zn(II), and Co(II) inhibit degradation of DNA by bleomycin and Fe(II) in the absence of added reducing agents. A model is proposed in which the degradation of DNA in these systems is dependent on the oxidation of an Fe(II)-bleomycin-DNA complex. © 1978, American Chemical Society. All rights reserved.
引用
收藏
页码:2740 / 2746
页数:7
相关论文
共 47 条
[1]   BLEOMYCIN-INDUCED BREAKAGE OF CLOSED-CIRCULAR DNA [J].
BEARDEN, JC ;
LLOYD, RS ;
HAIDLE, CW .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1977, 75 (02) :442-448
[2]  
BLUM RH, 1973, CANCER, V31, P903, DOI 10.1002/1097-0142(197304)31:4<903::AID-CNCR2820310422>3.0.CO
[3]  
2-N
[5]   PROTON NUCLEAR MAGNETIC-RESONANCE STUDY OF BLEOMYCIN IN AQUEOUS-SOLUTION - ASSIGNMENT OF RESONANCES [J].
CHEN, DM ;
HAWKINS, BL ;
GLICKSON, JD .
BIOCHEMISTRY, 1977, 16 (12) :2731-2738
[6]   BLEOMYCIN-DNA INTERACTIONS - FLUORESCENCE AND PROTON MAGNETIC-RESONANCE STUDIES [J].
CHIEN, M ;
GROLLMAN, AP ;
HORWITZ, SB .
BIOCHEMISTRY, 1977, 16 (16) :3641-3647
[7]   MECHANISM OF DEGRADATION OF DNA BY STREPTONIGRIN [J].
CONE, R ;
HASAN, SK ;
LOWN, JW ;
MORGAN, AR .
CANADIAN JOURNAL OF BIOCHEMISTRY, 1976, 54 (03) :219-223
[8]  
EMERY T, 1971, ADV ENZYMOL RAMB, V35, P135
[9]   EVIDENCE FOR SUPEROXIDE-DEPENDENT REDUCTION OF FE-3+ AND ITS ROLE IN ENZYME-GENERATED HYDROXYL RADICAL FORMATION [J].
FONG, KL ;
MCCAY, PB ;
POYER, JL ;
MISRA, HP ;
KEELE, BB .
CHEMICO-BIOLOGICAL INTERACTIONS, 1976, 15 (01) :77-89
[10]   MECHANISM OF OXYGENATION OF FERROUS ION IN NEUTRAL SOLUTION [J].
GOTO, K ;
TAMURA, H ;
NAGAYAMA, M .
INORGANIC CHEMISTRY, 1970, 9 (04) :963-&