Degen Christian, Ecker Josef, Piegholdt Stefanie, Liebisch Gerhard, Schmitz Gerd, Jahreis Gerhard
Friedrich Schiller University, Institute of Nutrition, Dept. of Nutritional Physiology, Jena, Germany.
Biochim Biophys Acta. 2011 Dec;1811(12):1070-80. doi: 10.1016/j.bbalip.2011.08.005. Epub 2011 Aug 26.
Conjugated fatty acids (CFAs) exhibit growth inhibitory effects on colon cancer in vitro and in vivo. To investigate whether the anticancerogenic potency depends on number or configuration of the conjugated double bonds, the effect of conjugated linoleic acid (CLA; C18:2) isomers and conjugated linolenic acid (CLnA; C18:3) isomers on viability and growth of HT-29 cells were compared. Low concentrations of CLnAs (<10μM) yielded a higher degree of inhibitory effects compared to CLAs (40μM). All trans-CFAs were more effective compared to cis/trans-CFAs as follows: t9,t11,t13-CLnA≥c9,t11,t13-CLnA>t11,t13-CLA≥t9,t11-CLA>c9,t11-CLA. The mRNA expression analysis of important genes associated with fatty acid metabolism showed an absence of ∆5-/∆6-desaturases and elongases in HT-29 cells, which was confirmed by fatty acid analysis. Using time- and dose-dependent stimulation experiments several metabolites were determined. Low concentrations of all trans-CFAs (5-20μM) led to dose-dependent increase of conjugated t/t-C16:2 formed by β-oxidation of C18 CFAs, ranging from 1-5% of total FAME. Importantly, it was found that CLnA is converted to CLA and that CLA is inter-converted (t11,t13-CLA is metabolized to c9,t11-CLA) by HT-29 cells. In summary, our study shows that growth inhibition of human cancer cells is associated with a specific cellular transcriptomic and metabolic profile of fatty acid metabolism, which might contribute to the diversified ability of CFAs as anti-cancer compounds.
共轭脂肪酸(CFAs)在体外和体内均对结肠癌具有生长抑制作用。为了研究抗癌效力是否取决于共轭双键的数量或构型,比较了共轭亚油酸(CLA;C18:2)异构体和共轭亚麻酸(CLnA;C18:3)异构体对HT-29细胞活力和生长的影响。与CLA(40μM)相比,低浓度的CLnAs(<10μM)产生了更高程度的抑制作用。所有反式CFAs比顺式/反式CFAs更有效,具体如下:t9,t11,t13-CLnA≥c9,t11,t13-CLnA>t11,t13-CLA≥t9,t11-CLA>c9,t11-CLA。对与脂肪酸代谢相关的重要基因进行的mRNA表达分析显示,HT-29细胞中不存在∆5-/∆6-去饱和酶和延长酶,脂肪酸分析证实了这一点。通过时间和剂量依赖性刺激实验确定了几种代谢物。低浓度的所有反式CFAs(5-20μM)导致由C18 CFAs的β-氧化形成的共轭t/t-C16:2呈剂量依赖性增加,占总脂肪酸甲酯的1-5%。重要的是,发现CLnA被HT-29细胞转化为CLA,并且CLA会相互转化(t11,t13-CLA代谢为c9,t11-CLA)。总之,我们的研究表明,人类癌细胞的生长抑制与脂肪酸代谢的特定细胞转录组和代谢谱相关,这可能有助于CFAs作为抗癌化合物的多样化能力。