G. Romano et al., Evaluation of polycyclic aromatic hydrocarbon-DNA adducts in exfoliated oral cells by an immunohistochemical assay, CANC EPID B, 8(1), 1999, pp. 91-96
Polycyclic aromatic hydrocarbon-DNA adducts were evaluated in oral cells fr
om 98 healthy volunteers by an immunohistochemical method using a specific
antiserum against benzo(a)pyrene-DNA adducts revealed by the immunoperoxida
se reaction. Mean adduct content, determined as relative staining intensity
by absorbance image analyzer, was significantly higher in the cells from t
obacco smokers compared with nonsmokers (330 +/- 98, n = 33 versus 286 +/-
83, n = 64, respectively) with a P = 0.013 obtained by two-sample t test wi
th equal variances, We found that in the smoker group, the PAH-DNA adduct c
ontent increases with the number of cigarettes. Thus, the relative staining
intensity was 305 +/- 105 in the group smoking 1-10 cigarettes/day (n = 16
), 347 +/- 77 in the 11-20 group (n = 14), and 386 +/- 112 in the group smo
king more than 20 cigarettes/day (n = 3; P = 0.03 by nonparametric test for
trend). No significant association was detected between PAH-DNA adducts in
oral cells and variables such as residential area, oral infections, alcoho
l or vitamin intake, grilled food consumption, and professional activity, T
his work confirms and extends previous data suggesting that this immunohist
ochemical method might be used as a valuable dosimeter of genotoxic damage
in a carcinogen-exposed population, although further studies are needed to
verify the applicability of the test in high-risk populations other than sm
okers.