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一种用于定量O-烷基化DNA加合物的高灵敏度和特异性方法及其在人体组织DNA分析中的应用。

A highly sensitive and specific method for quantitation of O-alkylated DNA adducts and its application to the analysis of human tissue DNA.

作者信息

Kang H, Konishi C, Kuroki T, Huh N

机构信息

Department of Cancer Cell Research, Institute of Medical Science, University of Tokyo, Japan.

出版信息

Environ Health Perspect. 1993 Mar;99:269-71. doi: 10.1289/ehp.9399269.

Abstract

Formation and accumulation of O6-alkylguanine and O4-alkylthymine in human tissues is possibly the most relevant marker for cancer risk. Because humans are chronically exposed to diverse kinds of chemicals and eventual DNA structural modifications are supposed to be a complex mixture of adducts at very low levels, it is essential to use an assay with extremely high sensitivity and specificity. We have established a quantitation method, called PREPI, for O6-methylguanine, O4-methylthymine, and O4-ethylthymine by the combination of prefractionation by HPLC, 32P-postlabeling, and immunoprecipitation. The detection limit was about 1 fmole for all three adducts, enabling us to analyze about 1 x 10(-8) levels as a molar ratio to normal counterpart using 100 micrograms of DNA. In a pilot experiment, we analyzed 11 peripheral blood samples from healthy volunteers. O6-Methylguanine was detected in all the cases with a mean value of 2.0 +/- 1.3 x 10(-8) (range, 0.78-4.6 x 10(-8)). Neither O4-methylthymine nor O4-ethylthymine was above the detection limit of 0.8 x 10(-8) as a ratio to thymine.

摘要

人体组织中O6 - 烷基鸟嘌呤和O4 - 烷基胸腺嘧啶的形成与积累可能是癌症风险最相关的标志物。由于人类长期接触多种化学物质,最终的DNA结构修饰被认为是极低水平加合物的复杂混合物,因此使用具有极高灵敏度和特异性的检测方法至关重要。我们通过高效液相色谱预分离、32P后标记和免疫沉淀相结合的方法,建立了一种用于定量O6 - 甲基鸟嘌呤、O4 - 甲基胸腺嘧啶和O4 - 乙基胸腺嘧啶的方法,称为PREPI。所有三种加合物的检测限约为1飞摩尔,这使我们能够使用100微克DNA以与正常对应物的摩尔比分析约1×10(-8)的水平。在一项初步实验中,我们分析了11名健康志愿者的外周血样本。所有样本中均检测到O6 - 甲基鸟嘌呤,平均值为2.0±1.3×10(-8)(范围为0.78 - 4.6×10(-8))。以与胸腺嘧啶的比例计,O4 - 甲基胸腺嘧啶和O4 - 乙基胸腺嘧啶均未超过0.8×10(-8)的检测限。

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