Ochoa Julio J, Farquharson Andrew J, Grant Ian, Moffat L E, Heys Steven D, Wahle Klaus W J
Institute of Nutrition and Food Technology, Department of Physiology, University of Granada, C/Ramon y Cajal 4, 18071, Granada, Spain.
Carcinogenesis. 2004 Jul;25(7):1185-91. doi: 10.1093/carcin/bgh116. Epub 2004 Feb 19.
The aims of this study were to examine the anti-proliferative effects of different concentrations of a commercial preparation of conjugated linoleic acids (CLA) mixture of isomers [cis-9, trans-11 CLA (c9,t11 CLA): trans-10, cis-12 CLA (50:50)] and their constituent isomers on PC-3, a human prostatic carcinoma cell line, and to study their effects on gene expression (mRNA and protein levels) of different enzymes and oncoproteins involved in oncogenesis and progression of prostate cancer. This includes pathways for arachidonic acid metabolism [cyclooxygenase 1 (COX-1), 2 (COX-2) and 5-lipoxygenase (5-LOX)], apoptosis (bcl-2) and cell cycle control (p21(WAF/Cip1)). Our results indicate a significant decrease in PC-3 proliferation elicited by CLA, although with high variability between isomers. The trans-10, cis-12 CLA was the most effective isomer (55% inhibition). This isomer was also able to decrease bcl-2 gene expression and to increase p21(WAF1/Cip1) mRNA levels (60% increase at highest concentration). In contrast, cis-9, trans-11 had no effect on these proteins but had a clear effect on 5-LOX expression and to a lesser degree on COX-2 protein level isomers. In conclusion, the anti-proliferative effects on PC-3 of CLA mixture and their constituent isomers are not equivalent, due to the different pathways involved for individual isomers. Trans-10, cis-12 seems to work preferentially through modulation of apoptosis and cell cycle control, while c9,t11 CLA isomer affects arachidonic acid metabolism.
本研究的目的是检测不同浓度的商业共轭亚油酸(CLA)异构体混合物[顺式-9,反式-11 CLA(c9,t11 CLA):反式-10,顺式-12 CLA(50:50)]及其组成异构体对人前列腺癌细胞系PC-3的抗增殖作用,并研究它们对参与前列腺癌发生和进展的不同酶和癌蛋白的基因表达(mRNA和蛋白质水平)的影响。这包括花生四烯酸代谢途径[环氧化酶1(COX-1)、2(COX-2)和5-脂氧合酶(5-LOX)]、细胞凋亡(bcl-2)和细胞周期调控(p21(WAF/Cip1))。我们的结果表明,CLA可显著降低PC-3的增殖,尽管异构体之间存在很大差异。反式-10,顺式-12 CLA是最有效的异构体(抑制率为55%)。该异构体还能够降低bcl-2基因表达并增加p21(WAF1/Cip1)mRNA水平(最高浓度时增加60%)。相比之下,顺式-9,反式-11对这些蛋白质没有影响,但对5-LOX表达有明显影响,对COX-2蛋白质水平异构体的影响较小。总之,由于各个异构体涉及的途径不同,CLA混合物及其组成异构体对PC-3的抗增殖作用并不等同。反式-10,顺式-12似乎主要通过调节细胞凋亡和细胞周期调控起作用,而c9,t11 CLA异构体则影响花生四烯酸代谢。