Farmer P B
MRC Toxicology Unit, University of Leicester, UK.
Clin Chem. 1994 Jul;40(7 Pt 2):1438-43.
Exposure to genotoxic carcinogens results in the formation of covalently bound adducts of the carcinogens with cellular nucleophilic molecules, including DNA and protein. Quantitative measurements of these adducts may be used to monitor exposure to these carcinogens. The analytical methods required to detect the adducts need to be of exceptional sensitivity and include 32P-postlabeling, immunoassay, and physicochemical techniques (e.g., mass spectrometry or fluorescence measurements). Owing to its accessibility and long lifetime, hemoglobin is also suitable for carcinogen adduct measurement, and techniques based on gas chromatography-mass spectrometry or immunoassay have been developed for this purpose. Although the measurement of adducts is now accepted as a valid means of monitoring exposure to carcinogens, the value of such measurements in indicating carcinogenic risk in humans is less certain. However, adduct concentrations, particularly at low doses of carcinogen, have in several instances been shown to correlate with tumorigenicity in animal experiments.
接触遗传毒性致癌物会导致致癌物与细胞亲核分子(包括DNA和蛋白质)形成共价结合加合物。对这些加合物进行定量测量可用于监测对这些致癌物的接触情况。检测这些加合物所需的分析方法需要具有极高的灵敏度,包括32P后标记法、免疫测定法和物理化学技术(如质谱法或荧光测量法)。由于血红蛋白易于获取且寿命较长,它也适用于致癌物加合物的测量,为此已开发出基于气相色谱 - 质谱法或免疫测定法的技术。尽管现在加合物的测量被公认为监测致癌物接触情况的有效手段,但此类测量在指示人类致癌风险方面的价值尚不确定。然而,在一些动物实验中,加合物浓度,尤其是在低剂量致癌物作用下的浓度,已被证明与致瘤性相关。