Endogenous and background DNA adducts by methylating and 2-hydroxyethylating agents

被引:47
作者
Zhao, CY
Tyndyk, M
Eide, I
Hemminki, K [1 ]
机构
[1] Karolinska Inst, Novum, Ctr Nutr & Toxicol, Dept Biosci, S-14157 Huddinge, Sweden
[2] NN Petrov Oncol Res Inst, St Petersburg 189646, Russia
[3] Statoil Res Ctr, N-7005 Trondheim, Norway
关键词
P-32-postlabelling; DNA adduct; 7-methylguanine; 7-(2-hydroxyethyl)guanine; HPLC;
D O I
10.1016/S0027-5107(99)00013-5
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Detection of 7-alkylguanine DNA adducts is useful to assess human exposure to and the resulting DNA damage caused by simple alkylating agents. The background 7-methylguanine (7-MG) and 7-hydroxyethylguanine (7-HEG) adduct levels were determined in human and rat tissues, using thin-layer chromatography (TLC) combined with high pressure liquid chromatography (HPLC). In addition, these two adduct levels were also compared in various tissues between smokers and non-smokers. The results demonstrated that the background level of 7-alkylguanine adducts in WBC and lung tissues of non-smokers was 2.9 and 4.0 adducts/10(7) nucleotides, respectively. In smokers with lung cancers 7-MG adduct level in lung samples (6.3 +/- 1.9 adducts/10(7) nucleotides) and in bronchus samples (6.1 +/- 1.5 adducts/10(7) nucleotides) was significantly higher than that in WBC samples (3.3 +/- 0.9 adducts/10(7) nucleotides). 7-HEG adduct levels obtained from the same individuals were 0.8 +/- 0.3 in lung, 1.0 +/- 0.8 in bronchus and 0.6 +/- 0.2 adducts/10(7) nucleotides in WBC, respectively. Animal studies showed that background levels of 7-MG (2.1-2.5 adducts/10(7) nucleotides) in control rats were approximately 2-4-fold higher than 7-HEG levels (0.6-0.9 adducts/10(7) nucleotides). After a 3-day exposure to 300 ppm ethene, 7-HEG adducts accumulated to a similar extent in different tissues of rats, with the mean adduct level of 5.6-7.0 in liver, 7.4 in lymphocytes and 5.5 adducts/10(7) nucleotides in kidney. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:117 / 125
页数:9
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