Growing evidence suggests that DNA repair capacity is an important factor i
n cancer risk and is therefore essential to assess. Immunochemical assays a
re amenable to the detection of repair products in complex matrices, such a
s urine, facilitating noninvasive measurements, although diet and extra-DNA
sources of lesion can confound interpretation. The production of single-st
randed, lesion-containing DNA oligomers characterises nucleotide excision r
epair (NER) and hence defines the repair pathway from which a lesion may be
derived. Herein we describe the characterisation of a monoclonal antibody
which recognises guanine moieties in single-stranded DNA. Application of th
is antibody in ELISA, demonstrated such oligomers in supernatants from repa
ir-proficient cells post-insult. Testing of urine samples from volunteers d
emonstrated a relationship between oligomer levels and two urinary DNA dama
ge products, thymine dimers and 8-oxo-2 ' -deoxyguanosine, supporting our h
ypothesis that NER gives rise to lesion-containing oligomers which are spec
ific targets for the investigation of DNA repair. (C) 2001 Academic Press.