Harris C C, Trump B F, Grafstrom R, Autrup H
J Cell Biochem. 1982;18(3):285-94. doi: 10.1002/jcb.1982.240180304.
The metabolism of chemical carcinogens has been studied in cultured human bronchus, colon, duodenum, pancreatic duct, and esophagus. Metabolite patterns and carcinogen-DNA adducts are generally qualitatively similar among animal species, individuals within a species, and tissues within an individual. However, wide quantitative differences are observed between individuals in outbred animal species, including humans. These interindividual differences in amounts of carcinogen-DNA adducts and in activities of enzymes that are important in the metabolism of chemical carcinogens are similar in magnitude (10-to 150-fold) to those observed in pharmacogenetic studies of drug metabolism. The role of these differences as risk factors in human cancer is being investigated.
已在培养的人支气管、结肠、十二指肠、胰管和食管中研究了化学致癌物的代谢。代谢物模式和致癌物 - DNA加合物在动物物种之间、物种内的个体之间以及个体内的组织之间通常在质量上相似。然而,在包括人类在内的远交动物物种的个体之间观察到了很大的数量差异。致癌物 - DNA加合物的量以及在化学致癌物代谢中起重要作用的酶的活性方面的这些个体间差异,其幅度(10至150倍)与药物代谢的药物遗传学研究中观察到的差异相似。正在研究这些差异作为人类癌症风险因素的作用。