Povey A C, Schiffman M, Taffe B G, Harris C C
Carcinogenesis Department, Christie Hospital and Holt Radium Institute, Manchester, Great Britain.
Mutat Res. 1991 Mar-Apr;259(3-4):387-97. doi: 10.1016/0165-1218(91)90129-a.
Fecapentaenes are a class of conjugated ether lipids which have been identified as the major component of human fecal mutagenicity in the Ames Salmonella mutagenesis assay. Human epidemiologic data have indicated that most healthy North American populations eating a western diet do excrete detectable levels of fecapentaenes. Excreted fecapentaene levels seem to reflect levels throughout the colonic lumen, and levels vary characteristically between individuals. Those individuals found to excrete high levels of fecapentaene appear, based on limited data, to be at decreased risk of colorectal neoplasia. Carcinogenicity studies in rats and mice have been predominantly negative, however, increased tumor incidence in mice exposed to fecapentaenes as neonates has recently been reported. Fecapentaenes are direct-acting genotoxins, which may react with DNA through free radical mechanisms, and/or aldehyde formation. Mechanisms by which fecapentaene-induced DNA damage may mediate carcinogenesis are discussed.
粪便五烯是一类共轭醚脂质,在艾姆斯沙门氏菌诱变试验中已被确定为人类粪便致突变性的主要成分。人类流行病学数据表明,大多数食用西方饮食的健康北美人群确实会排出可检测水平的粪便五烯。排出的粪便五烯水平似乎反映了整个结肠腔的水平,而且个体之间的水平具有特征性差异。根据有限的数据,那些被发现排出高水平粪便五烯的个体患结直肠癌的风险似乎较低。然而,对大鼠和小鼠的致癌性研究大多为阴性,不过最近有报道称,新生小鼠接触粪便五烯后肿瘤发病率增加。粪便五烯是直接作用的基因毒素,可能通过自由基机制和/或醛的形成与DNA发生反应。本文讨论了粪便五烯诱导的DNA损伤可能介导致癌作用的机制。