Studies on the chemical reactivity of copper bleomycin. J Inorg Biochem 1982 Oct;17(2):75-94
Date
10/01/1982Pubmed ID
6184448DOI
10.1016/s0162-0134(00)80077-xScopus ID
2-s2.0-0020307487 (requires institutional sign-in at Scopus site) 20 CitationsAbstract
The copper(II) complex of the clinically used antitumor agent bleomycin (Blm) has cytotoxic as well as antitumor properties. To understand the relationship of the bleomycin ligand, copper bleomycin, and other possible metal complexes of this agent, kinetic studies of the formation of Cu(II)Blm, ligand substitution reactions of CuBlm with ethylenediaminetetraaletic acid, and the redox reaction of CuBlm with thiols have been completed and interpreted along with previous studies of the thermodynamic stability of Cu2+ with bleomycin. Cu(II)Bm is found to be kinetically and thermodynamically stable in ligand substitution processes and is only slowly reduced and dissociated by sulfhydryl reagents. The rate constant of reduction of the complex by 2-mercaptoethanol (2-ME) at pH 7.4 and 25 degrees C is 9.5 X 10(-3) M-1 sec-1, explaining the inhibition of Fe2+-dependent strand scission of DNA by Cu2+ in the presence of 2-ME. CuBlm forms in preference to Fe(II)Blm and cannot be reduced and dissociated rapidly enough by thiols to liberate Blm and form the reactive iron complex. In agreement with the observed chemical stability of CuBlm, it is also shown that the complex is stable in human plasma and in the presence of Ehrlich cells suspended in ascites fluid. Interestingly, little CuBlm enters these cells to carry out cytotoxic reactions. Finally, it is shown that both Cu2+ and Zn2+, at equivalent concentrations to Fe2+, effectively inhibit the strand scission of DNA by Fe(II)Blm plus oxygen. However, at substoichiometric amounts of Cu2+, the ferroxidase activity of Blm enables the drug to remain effective in the strand-scission reaction, despite the lowered Cu-free Blm/Fe2+ ratio. These results are discussed in light of the proposed mechanism of action of bleomycin.
Author List
Antholine WE, Solaiman D, Saryan LA, Petering DHMESH terms used to index this publication - Major topics in bold
AnimalsAntineoplastic Agents
Bleomycin
Carcinoma, Ehrlich Tumor
Chemical Phenomena
Chemistry
DNA
Humans
In Vitro Techniques
Kinetics
Ligands
Mice
Oxidation-Reduction
Sulfhydryl Compounds
