van Schooten F J, Hillebrand M J, van Leeuwen F E, Lutgerink J T, van Zandwijk N, Jansen H M, Kriek E
Division of Chemical Carcinogenesis, The Netherlands Cancer Institute, Antoni van Leeuwenhoek Huis, Amsterdam.
Carcinogenesis. 1990 Sep;11(9):1677-81. doi: 10.1093/carcin/11.9.1677.
In an attempt to probe for polycyclic aromatic hydrocarbon (PAH)-DNA adducts in human subjects resulting from smoking (or other chronic environmental exposure), lung tissue and lung tumours were obtained from patients hospitalized for lung cancer. DNA was isolated from the tissue samples and examined both in an ELISA using a polyclonal antibody against (+/-)trans-7,8-dihydroxy-anti-9,10-epoxy-7,8,9,10- tetrahydrobenzo[a]pyrene (BPDE)-DNA as well as by the nuclease P1-mediated modification of the 32P-post-labelling technique. The ELISA results showed BPDE-DNA antigenicity in lung DNA from 6 out of 21 patients, and adduct levels ranged from 2 to 134 adducts per 10(8) nucleotides. For all 21 patients, the autoradiographs of chromatograms of 32P-postlabelled digests of DNA from non-tumorous lung tissue showed a strong diagonal radioactive zone (DRZ). This DRZ was generally absent in tumorous tissue. DNA samples that were positive in the ELISA contained a dominant spot within the DRZ that co-chromatographed with the major BPDE-DNA adduct (BPDE-dG). The quantities of the BPDE-dG spots ranged from 2.1 to 42 adducts in 10(9) nucleotides. These values were lower than the levels found in the ELISA but correlated well with the ELISA results (Kendall W = 0.97; P = 0.00). The levels of the DRZ adducts ranged from 1.9 to 34 adducts in 10(8) nucleotides. Correlations between smoking and DNA adduct levels were poor because of the small number of current smokers (n = 13). However, smokers of filter cigarettes had significantly lower DNA adduct levels compared with smokers of cigarettes without a filter (P = 0.02 by Fischer's exact test).
为了探究吸烟(或其他慢性环境暴露)导致的人体多环芳烃(PAH)-DNA加合物情况,从因肺癌住院的患者身上获取了肺组织和肺肿瘤组织。从组织样本中分离出DNA,并使用针对(±)反式-7,8-二羟基-反式-9,10-环氧-7,8,9,10-四氢苯并[a]芘(BPDE)-DNA的多克隆抗体,通过酶联免疫吸附测定(ELISA)以及核酸酶P1介导的32P后标记技术对其进行检测。ELISA结果显示,21名患者中有6名患者的肺DNA存在BPDE-DNA抗原性,加合物水平为每10⁸个核苷酸2至134个加合物。对于所有21名患者,非肿瘤肺组织DNA的32P后标记消化产物色谱图的放射自显影片显示出一个强烈的对角放射性区域(DRZ)。肿瘤组织中通常没有这个DRZ。ELISA呈阳性的DNA样本在DRZ内有一个占主导地位的斑点,其色谱行为与主要的BPDE-DNA加合物(BPDE-dG)相同。BPDE-dG斑点的数量在每10⁹个核苷酸中为2.1至42个加合物。这些值低于ELISA中发现的水平,但与ELISA结果相关性良好(肯德尔W = 0.97;P = 0.00)。DRZ加合物水平在每10⁸个核苷酸中为1.9至34个加合物。由于当前吸烟者数量较少(n = 13),吸烟与DNA加合物水平之间的相关性较差。然而,过滤嘴香烟吸烟者的DNA加合物水平明显低于无过滤嘴香烟吸烟者(费舍尔精确检验P = 0.02)。