Djuric Zora, Aslam Muhammad Nadeem, Simon Becky R, Sen Ananda, Jiang Yan, Ren Jianwei, Chan Rena, Soni Tanu, Rajendiran T M, Smith William L, Brenner Dean E
Department of Family Medicine, University of Michigan, Ann Arbor, MI 48109, USA.
Department of Pathology, University of Michigan, Ann Arbor, MI 48109, USA.
J Nutr Biochem. 2017 Aug;46:90-99. doi: 10.1016/j.jnutbio.2017.04.013. Epub 2017 Apr 25.
Dietary fish oils have potential for prevention of colon cancer, and yet the mechanisms of action in normal and tumor colon tissues are not well defined. Here we evaluated the impact of the colonic fatty acid milieu on the formation of prostaglandins and other eicosanoids. Distal tumors in rats were chemically induced to model inflammatory colonic carcinogenesis. After 21 weeks of feeding with either a fish oil diet containing an eicosapentaenoic acid/ω-6 fatty acid ratio of 0.4 or a Western fat diet, the relationships between colon fatty acids and prostaglandin E (PGE) concentrations were evaluated. PGE is a key proinflammatory mediator in the colon tightly linked with the initiation and progression of colon cancer. The fish oil vs. the Western fat diet resulted in reduced total fatty acid concentrations in serum but not in colon. In the colon, the effects of the fish oil on fatty acids differed in normal and tumor tissue. There were distinct lipodomic patterns consistent with a lipogenic phenotype in tumors. In tumor tissue, the eicosapentaenoic acid/arachidonic acid ratio, cyclooxygenase-2 expression and the mole percent of saturated fatty acids were significant predictors of inter-animal variability in colon PGE after accounting for diet. In normal tissues from either control rats or carcinogen-treated rats, only diet was a significant predictor of colon PGE. These results show that the fatty acid milieu can modulate the efficacy of dietary fish oils for colon cancer prevention, and this could extend to other preventive agents that function by reducing inflammatory stress.
膳食鱼油具有预防结肠癌的潜力,然而其在正常和肿瘤结肠组织中的作用机制尚未明确。在此,我们评估了结肠脂肪酸环境对前列腺素和其他类二十烷酸形成的影响。通过化学诱导大鼠远端肿瘤来模拟炎症性结肠癌发生过程。在用二十碳五烯酸/ω-6脂肪酸比例为0.4的鱼油饮食或西方高脂饮食喂养21周后,评估结肠脂肪酸与前列腺素E(PGE)浓度之间的关系。PGE是结肠中一种关键的促炎介质,与结肠癌的发生和发展密切相关。鱼油与西方高脂饮食相比,导致血清中总脂肪酸浓度降低,但结肠中未降低。在结肠中,鱼油对脂肪酸的影响在正常组织和肿瘤组织中有所不同。肿瘤中存在与脂肪生成表型一致的独特脂质组学模式。在肿瘤组织中,在考虑饮食因素后,二十碳五烯酸/花生四烯酸比例、环氧化酶-2表达和饱和脂肪酸的摩尔百分比是动物间结肠PGE变异性的显著预测因子。在对照大鼠或致癌物处理大鼠的正常组织中,只有饮食是结肠PGE的显著预测因子。这些结果表明,脂肪酸环境可以调节膳食鱼油预防结肠癌的功效,这可能也适用于其他通过减轻炎症应激发挥作用的预防剂。