Schiffman M H, Van Tassell R L, Andrews A W, Wacholder S, Daniel J, Robinson A, Smith L, Nair P P, Wilkins T D
Epidemiology and Biostatistics Program, National Cancer Institute, Bethesda, MD 20892.
Mutat Res. 1989 Apr;222(4):351-7. doi: 10.1016/0165-1218(89)90111-0.
The fecapentaenes (FP) are the predominant fecal mutagens identified to date, but they have not been shown to be carcinogenic. Epidemiologists looking for other fecal mutagens that may be related to colorectal cancer must disentangle from their investigations the pervasive mutagenic effect of the fecapentaenes. As a first step to studying the epidemiology of fecal mutagenicity independent of fecapentaenes, we compared FP measurements and Salmonella mutagenicity assay results for 718 acetone-extracted stool samples collected from a variety of subjects in the Washington DC metropolitan areas. In this large group, 50% of mutagenic samples contained elevated fecapentaenes. Specifically, three-quarters of the samples mutagenic in TA100 contained high FP levels. In contrast, mutagenicity in TA98 was not generally explainable by fecapentaenes, suggesting that non-fecapentaene TA98 mutagenicity should be one focus of future efforts to uncover colorectal carcinogens of etiologic importance.
粪五烯(FP)是迄今为止已确定的主要粪便诱变剂,但尚未证明它们具有致癌性。寻找可能与结直肠癌相关的其他粪便诱变剂的流行病学家必须在其调查中排除粪五烯普遍存在的诱变作用。作为独立于粪五烯研究粪便诱变性流行病学的第一步,我们比较了从华盛顿特区大都市区的各类受试者收集的718份丙酮提取粪便样本的FP测量值和沙门氏菌诱变性试验结果。在这个大群体中,50%的诱变样本中粪五烯含量升高。具体而言,在TA100中具有诱变性的样本中有四分之三的FP水平较高。相比之下,TA98中的诱变性通常无法用粪五烯来解释,这表明非粪五烯的TA98诱变性应成为未来揭示具有病因学重要性的结直肠癌致癌物的努力重点之一。