Adriamycin is known to induce the formation of adducts with DNA when r
eacted under in vitro transcription conditions. The factors affecting
the extent of adduct formation were examined in order to establish the
critical components and optimal conditions required for the reaction,
and to gain insight into the nature of the DNA-adduct complex. There
was a strong dependence on reaction temperature (with a 40-fold increa
se of adducts at 40-50 degrees C compared to 10 degrees C), pH (maximu
m adducts at pH 7), but little dependence on the oxygen level. There w
as an absolute requirement for a reducing agent, with adducts detected
with DTT, beta-mercaptoethanol and glutathione, maximal adducts were
formed at high levels of DTT (5-10 mM). Adducts were also formed with
a xanthine oxidase/NADH reducing system, with increasing amounts of ad
ducts detected with increasing NADH; no adducts were detected in the a
bsence of either the enzyme or NADH. Of fourteen derivatives studied,
only four yielded a similar extent of adduct formation as adriamycin;
there was no absolute requirement for a carbonyl at C13 or hydroxyl at
C14. Adducts were also observed with ssDNA but required a longer reac
tion time compared to dsDNA. The sequence specificity of adduct format
ion with ssDNA was examined using a primer-extension assay; almost all
adducts were associated with a guanine residue. Overall, the results
are consistent with a two-step reaction mechanism involving reductive
activation of adriamycin, with the activated species then reacting wit
h the guanine residues of either dsDNA or ssDNA.