Paz-Elizur Tamar, Krupsky Meir, Blumenstein Sara, Elinger Dalia, Schechtman Edna, Livneh Zvi
Department of Biological Chemistry, Weizmann Institute of Science, Rehovot, Israel.
J Natl Cancer Inst. 2003 Sep 3;95(17):1312-9. doi: 10.1093/jnci/djg033.
Although smoking is a major cause of lung cancer, only a proportion of smokers develop lung cancer, suggesting a genetic predisposition in some individuals. Because tobacco smoking is associated with the increased formation of DNA lesions, including those induced from oxidative damage, we investigated whether the activity of the DNA repair enzyme 8-oxoguanine DNA N-glycosylase (OGG), which repairs the oxidative DNA lesion 8-oxoguanine, is associated with lung cancer.
We conducted a molecular epidemiologic case-control study that included 68 case patients with non-small-cell lung cancer and 68 healthy control subjects, frequency matched for age and sex. Enzymatic OGG activity was determined in protein extracts prepared from peripheral blood mononuclear cells or lung tissue by assaying the cleavage product of a radiolabeled synthetic DNA oligonucleotide containing an 8-oxoguanine residue. Odds ratios (ORs) and 95% confidence intervals (CIs) were determined by conditional logistic regression. All statistical tests were two-sided.
OGG activity was lower in peripheral blood mononuclear cells from case patients than in those from control subjects. After adjustment for age and smoking status, individuals in the lowest tertile of OGG activity had an increased risk of non-small-cell lung cancer compared with individuals in the highest tertile (OR = 4.8, 95% CI = 1.5 to 15.9). The adjusted OR associated with a unit decrease in OGG activity was statistically significantly increased (OR = 1.9, 95% CI = 1.3 to 2.8). There was no interaction between OGG activity and smoking status. The estimated relative risk of lung cancer for smokers with low OGG activity was 34- or 124-fold higher for smokers with a low OGG activity of 6.0 or 4.0 U/ micro g protein, respectively, than for nonsmokers with a normal OGG activity of 7.0 U/ micro g protein, illustrating the cumulative effect of low OGG activity and smoking.
Low OGG activity is associated with an increased risk of lung cancer. Although prospective studies are needed to validate the results, they suggest that smoking cessation in individuals with reduced OGG activity might be an effective strategy in lung cancer prevention.
尽管吸烟是肺癌的主要病因,但只有一部分吸烟者会患肺癌,这表明某些个体存在遗传易感性。由于吸烟与DNA损伤的形成增加有关,包括氧化损伤诱导的损伤,我们研究了修复氧化DNA损伤8-氧鸟嘌呤的DNA修复酶8-氧鸟嘌呤DNA糖基化酶(OGG)的活性是否与肺癌有关。
我们进行了一项分子流行病学病例对照研究,纳入了68例非小细胞肺癌患者和68名健康对照者,年龄和性别进行了频率匹配。通过检测含有8-氧鸟嘌呤残基的放射性标记合成DNA寡核苷酸的切割产物,在外周血单核细胞或肺组织制备的蛋白质提取物中测定酶促OGG活性。通过条件逻辑回归确定比值比(OR)和95%置信区间(CI)。所有统计检验均为双侧检验。
病例患者外周血单核细胞中的OGG活性低于对照者。在调整年龄和吸烟状态后,OGG活性处于最低三分位数的个体与最高三分位数的个体相比,患非小细胞肺癌的风险增加(OR = 4.8,95% CI = 1.5至15.9)。与OGG活性单位降低相关的调整后OR在统计学上显著增加(OR = 1.9,95% CI = 1.3至2.8)。OGG活性与吸烟状态之间没有相互作用。OGG活性低的吸烟者患肺癌的估计相对风险分别比OGG活性正常为7.0 U/μg蛋白质的非吸烟者高34倍或124倍,这取决于OGG活性低至6.0或4.0 U/μg蛋白质,说明了低OGG活性和吸烟的累积效应。
低OGG活性与肺癌风险增加有关。尽管需要前瞻性研究来验证结果,但这些结果表明,OGG活性降低的个体戒烟可能是预防肺癌的有效策略。