Lung cancer is the leading cause of cancer mortality in Taiwanese women. Ci
garette smoking cannot explain the high lung cancer mortality in this popul
ation because less than 10% of women in Taiwan are smokers. Therefore, envi
ronmental Factors other than smoking may play an important role in lung can
cer development in female nonsmokers. The purpose of this study was to eluc
idate the role of environmental carcinogen exposure in lung cancer developm
ent in Taiwanese female nonsmokers, based on DNA adduct Formation. We colle
cted nontumorous lung tissues resected From 62 nonsmoking lung cancer patie
nts and 20 noncancer controls to investigate whether differences in suscept
ibility to DNA adduct formation exist between men and women. P-32-postlabel
ing and ELISA (enzyme-linked immunosorbent assay) with polyclonal antibody
against BPDE (7,81-dihydroxy-anti-9,10epoxy-7, 8,9,10-tetrahydrobenzo[a] py
re ne)-DNA adduct were used to evaluate DNA adduct levels in lung tissues o
f study subjects. Our data showed that the DNA adduct levels of lung cancer
patients determined both assays were significantly higher than those of no
ncancer controls (P = 0.0001 for P-32-postlabeling; P = 0.01 For ELISA). Mo
reover, DNA adduct levels in females were markedly greater than those in ma
les (P = 0.014 for P-32-postlabeling; P = 0.001 For ELISA). The difference
in DNA adduct levels could not be explained by genetic polymorphisms of cyt
ochrome P-4501Al (CYP1Al) or glutathione S-transferase (GSTM1), as determin
ed by polymerase chain reaction and restriction fragment length polymorphis
m. These results demonstrate that lung cancer patients have a higher suscep
tibility to DNA damage than that of noncancer controls. In addition, differ
ences in susceptibility to DNA damage derived From environmental carcinogen
exposure were observed between male and Female nonsmokers. In conclusion,
high susceptibility to DNA damage in Females may partially explain the high
mortality rate of lung cancer in nonsmoking Taiwanese women. (C) 2001 Wile
y-Liss, Inc.