The ratio of deoxyadenosine to deoxyguanosine adducts formed by (+)-(7R, 8S, 9S, 10R)-7,8-dihydroxy-9,10-epoxy-7,8,9,10-tetrahydrobenzo[a]pyrene in purified calf thymus DNA and DNA in V-79 cells is independent of dose

Citation
Sjc. Wei et al., The ratio of deoxyadenosine to deoxyguanosine adducts formed by (+)-(7R, 8S, 9S, 10R)-7,8-dihydroxy-9,10-epoxy-7,8,9,10-tetrahydrobenzo[a]pyrene in purified calf thymus DNA and DNA in V-79 cells is independent of dose, INT J ONCOL, 14(3), 1999, pp. 509-513
Citations number
14
Categorie Soggetti
Onconogenesis & Cancer Research
Journal title
INTERNATIONAL JOURNAL OF ONCOLOGY
ISSN journal
10196439 → ACNP
Volume
14
Issue
3
Year of publication
1999
Pages
509 - 513
Database
ISI
SICI code
1019-6439(199903)14:3<509:TRODTD>2.0.ZU;2-S
Abstract
The hypothesis that the decrease in the proportion of mutations at AT base pairs in Chinese hamster V-79 cells treated with increasing doses of (+)-(R ,S,S,R)-benzo[a]pyrene diol epoxide ((+)-BPDE) is due to saturation of A 'h ot spots' for adduct formation was investigated by comparing the ratio of d A to dG adducts formed at high (0.48 mu M) and low (0.04 mu M) doses of [H- 3]-labeled (+)-BPDE. The dA to dG adduct ratio was similar in both calf thy mus DNA and the genomic DNA in V-79 cells, and did not change with dose. Fo r the V-79 cells, this ratio was also unaffected by a 24-h post treatment r epair incubation.