Schiffman M H, Andrews A W, Van Tassell R L, Smith L, Daniel J, Robinson A, Hoover R N, Rosenthal J, Weil R, Nair P P
Epidemiology and Biostatistics Program, Division of Cancer Etiology, National Cancer Institute, Bethesda, Maryland 20892.
Cancer Res. 1989 Jun 15;49(12):3420-4.
Fecal mutagenicity was measured in 68 patients with colorectal cancer and in 114 controls, using Salmonella tester strains TA98 and TA100 with and without S9 activation. Samples were also tested for fecapentaenes by high-performance liquid chromatography, to permit the separation of fecapentaene and non-fecapentaene mutagenicity. Overall, no significant case-control differences in fecal mutagenicity were observed. However, when samples containing high concentrations of fecapentaenes were excluded, non-fecapentaene TA98 mutagenicity was observed in eight cases (12%) and only four controls (4%), resulting in an estimated relative risk of 4.4 (95% confidence interval = 1.0-21.1). The association of colorectal cancer risk with non-fecapentaene TA98 mutagenicity could not be explained as an artifact of diagnostic workup or gastrointestinal bleeding among the cases. Smoking could also be excluded as a source of the TA98 mutagenicity seen, but possible dietary origins are still being explored.
使用带有和不带有S9激活的鼠伤寒沙门氏菌测试菌株TA98和TA100,对68例结直肠癌患者和114名对照者进行粪便致突变性检测。还通过高效液相色谱法对粪便戊烯进行检测,以区分粪便戊烯和非粪便戊烯的致突变性。总体而言,未观察到粪便致突变性方面显著的病例对照差异。然而,当排除含有高浓度粪便戊烯的样本后,在8例患者(12%)中观察到非粪便戊烯TA98致突变性,而在对照者中仅4例(4%)观察到,估计相对风险为4.4(95%置信区间 = 1.0 - 21.1)。结直肠癌风险与非粪便戊烯TA98致突变性之间的关联不能解释为病例诊断检查或胃肠道出血造成的假象。吸烟也可排除为所见TA98致突变性的来源,但仍在探索可能的饮食来源。