Oxidative damage to cellular biomolecules, in particular DNA, has been prop
osed to play an important role in a number of pathological conditions, incl
uding carcinogenesis. A much studied consequence of oxygen-centred radical
damage to DNA is 8-oxo-2'-deoxyguanosine (8-oxodG). Using numerous techniqu
es, this lesion has been quantified in various biological matrices, most no
tably DNA and urine. Until recently, it was understood that urinary 8-oxodG
derives solely from DNA repair, although the processes which may yield the
modified deoxynucleoside have never been thoroughly discussed. This review
suggests that nucleotide excision repair and the action of a specific endo
nuclease may, in addition to the nucleotide pool, contribute significantly
to levels of 8-oxodG in the urine. On this basis, urinary 8-oxodG represent
s an important biomarker of generalised, cellular oxidative stress. Current
data from antioxidant supplementation trials are examined and the potentia
l for such compounds to modulate DNA repair is considered. It is stressed t
hat further work is required to link DNA, serum and urinary levels of 8-oxo
dG such that the kinetics of formation and clearance may be elucidated, fac
ilitating greater understanding of the role played by oxidative stress in d
isease.