Carcinogenesis, Vol 19, 147-155, Copyright © 1998 by Oxford University Press
M Gamberini, MR Cidade, LA Valotta, MC Armelin and LC Leite
Several hydrazine derivatives (HD) tested so far have pharmacological
activities, but many also have toxic side effects, including
carcinogenesis. Their toxicity has been ascribed to carbocations (via
formation of azoxy intermediates), alkyl radicals or reactive oxygen
species. Cytotoxicity and transformation by carbocations is widely
accepted, but the role of alkyl radicals is still questioned. We have
investigated the cytotoxicity of HD to mouse fibroblasts in three
activation systems in which enhanced alkyl radical formation is
demonstrated by electron spin resonance/spin-trapping. Cytotoxicity was
assayed by inhibition of [3H-methyl]thymidine uptake into DNA of Balb/c 3T3
and/or Myc 9E fibroblasts (normal Balb/c 3T3 cells over-expressing the
c-myc proto-oncogene). Based on the results obtained in the cytotoxicity
assays we also investigated the transforming potential of procarbazine
(PCZ) and methylhydrazine (MeH) activated by horseradish peroxidase (HRP)
using the Myc 9E cell line, which aims at the activation of a second
cooperating oncogene. Our results show that: (i) cytotoxicity of HD to
mouse fibroblasts is increased by HRP activation of MeH, phenelzine and
PCZ, which displayed enhanced alkyl radical formation, but not of
1,2-dimethylhydrazine (DMH), which did not produce increased alkyl radical
formation under these conditions; (ii) cytotoxicity of neutrophil-activated
MeH (producing a 10-fold higher concentration of methyl radicals), is more
pronounced than DMH; (iii) MeH and DMH activated by prolonged
auto-oxidation in 24-h incubations have comparable cytotoxicity and alkyl
radical formation; and (iv) PCZ and MeH activation by HRP to alkyl radicals
increased the transformation induced in Myc 9E cells. Taken together, our
results strongly support a role for hydrazine-derived alkyl radicals in HD-
induced cytotoxicity and cell transformation.
ARTICLES
Contribution of hydrazines-derived alkyl radicals to cytotoxicity and transformation induced in normal c-myc-overexpressing mouse fibroblasts
Centro de Biotecnologia, Instituto Butantan, Sao Paulo, Brasil.
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