Koronowicz Aneta A, Banks Paula, Master Adam, Domagała Dominik, Piasna-Słupecka Ewelina, Drozdowska Mariola, Sikora Elżbieta, Laidler Piotr
Department of Human Nutrition, Faculty of Food Technology, University of Agriculture in Krakow, Balicka 122, 30-149 Krakow, Poland.
Department of Biochemistry and Molecular Biology, Medical Centre for Postgraduate Education, Marymoncka 99, 01-813 Warsaw, Poland.
PPAR Res. 2017;2017:2865283. doi: 10.1155/2017/2865283. Epub 2017 Mar 26.
In our previous study, we showed that fatty acids from CLA-enriched egg yolks (EFA-CLA) reduced the proliferation of breast cancer cells; however, the molecular mechanisms of their action remain unknown. In the current study, we used MCF-7 breast cancer cell line to determine the effect of EFA-CLA, as potential ligands for peroxisome proliferator-activated receptors (PPARs), on identified in silico PPAR-responsive genes: , , , , and (transcript TR2). Our results showed that EFA-CLA act as PPAR ligands with agonistic activity for all PPAR isoforms, with the highest specificity towards PPAR. In conclusion, we propose that EFA-CLA-mediated regulation of PPAR-responsive genes is most likely facilitated by isomer incorporated in egg yolk. Notably, EFA-CLA activated PPAR more efficiently than nonenriched FA as well as synthetic CLA isomers. We also propose that this regulation, at least in part, can be responsible for the observed reduction in the proliferation of MCF-7 cells treated with EFA-CLA.
在我们之前的研究中,我们发现富含共轭亚油酸的蛋黄脂肪酸(EFA-CLA)可降低乳腺癌细胞的增殖;然而,其作用的分子机制仍不清楚。在本研究中,我们使用MCF-7乳腺癌细胞系来确定作为过氧化物酶体增殖物激活受体(PPARs)潜在配体的EFA-CLA对计算机识别的PPAR反应性基因: 、 、 、 和 (转录本TR2)的影响。我们的结果表明,EFA-CLA作为PPAR配体,对所有PPAR亚型均具有激动活性,对PPAR的特异性最高。总之,我们认为EFA-CLA介导的PPAR反应性基因调控很可能是由蛋黄中所含的 异构体促成的。值得注意的是,EFA-CLA比未富集的脂肪酸以及合成CLA异构体更有效地激活PPAR。我们还认为,这种调控至少部分地可解释在用EFA-CLA处理的MCF-7细胞中观察到的增殖减少现象。