Oshima M, Takahashi M, Oshima H, Tsutsumi M, Yazawa K, Sugimura T, Nishimura S, Wakabayashi K, Taketo M M
Banyu Tsukuba Research Institute (Merck), Japan.
Carcinogenesis. 1995 Nov;16(11):2605-7. doi: 10.1093/carcin/16.11.2605.
Epidemiological studies and animal experiments show an association of dietary intake of fish oils and low incidence of several types of cancers. The active ingredients of fish oils appear to be polyunsaturated fatty acids of omega-3 type such as eicosapentaenoic acid and docosahexaenoic acid (DHA). We have investigated chemopreventive effects of DHA on mouse intestinal polyposis using adenomatous polyposis coli (Apc) gene knockout mice. Damage to the human APC gene is responsible for not only familial adenomatous polyposis but also many sporadic cancers of the entire digestive tract. Using homologous recombination in embryonic stem cells, we recently constructed gene knockout mice containing a truncation mutation in the Apc gene at codon 716 (Apc delta 716). The heterozygous mice developed numerous intestinal polyps, and all microadenomas dissected from the earliest polyps had already lost the wild-type allele, indicating the loss of heterozygosity [Oshima et al. (1995), Proc. Natl Acad. Sci. USA, 92, 4482-4486]. We fed Apc delta 716 heterozygotes with AIN-76A purified diet containing 3% DHA for 7 weeks, and scored the number and size of intestinal polyps. Average DHA intakes per day were 4.1 and 4.3 g/kg body wt for males and females, respectively. DHA-fed females had only 31% of polyps compared with the control females that developed about 220 polyps, whereas DHA-fed females showed no significant decrease in the polyp number. As for the polyp size, the proportion of larger polyps decreased more significantly in females than in males. This is the first demonstration that DHA inhibits intestinal polyposis induced by an Apc mutation at both its formation and growth.
流行病学研究和动物实验表明,摄入鱼油与几种癌症的低发病率相关。鱼油的活性成分似乎是ω-3型多不饱和脂肪酸,如二十碳五烯酸和二十二碳六烯酸(DHA)。我们使用腺瘤性息肉病大肠杆菌(Apc)基因敲除小鼠,研究了DHA对小鼠肠道息肉病的化学预防作用。人类APC基因的损伤不仅导致家族性腺瘤性息肉病,还导致整个消化道的许多散发性癌症。利用胚胎干细胞中的同源重组,我们最近构建了在密码子716处Apc基因含有截短突变的基因敲除小鼠(Apc delta 716)。杂合子小鼠出现了大量肠道息肉,从最早的息肉中分离出的所有微腺瘤都已经失去了野生型等位基因,表明杂合性缺失[大岛等人(1995年),《美国国家科学院院刊》,92,4482 - 4486]。我们用含有3% DHA的AIN - 76A纯化饮食喂养Apc delta 716杂合子7周,并对肠道息肉的数量和大小进行评分。雄性和雌性每天的平均DHA摄入量分别为4.1和4.3 g/kg体重。与发育出约220个息肉的对照雌性相比,喂食DHA的雌性只有31%的息肉,而喂食DHA的雌性息肉数量没有显著减少。至于息肉大小,雌性中较大息肉的比例下降比雄性更显著。这首次证明了DHA在肠道息肉的形成和生长过程中均抑制由Apc突变诱导的肠道息肉病。