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反增殖和促凋亡的作用的 trans9, trans11 共轭亚油酸异构体对 MCF-7 乳腺癌细胞与 LXR 激活有关。

The anti-proliferative and pro-apoptotic effects of the trans9, trans11 conjugated linoleic acid isomer on MCF-7 breast cancer cells are associated with LXR activation.

机构信息

EA2160, Mer, Molécules, Santé, IUML: Institut Universitaire Mer et Littoral FR3473 CNRS, Faculty of Pharmacy, Nantes, France.

出版信息

Prostaglandins Leukot Essent Fatty Acids. 2013 Apr;88(4):265-72. doi: 10.1016/j.plefa.2012.12.006. Epub 2013 Feb 1.

DOI:10.1016/j.plefa.2012.12.006
PMID:23375583
Abstract

Conjugated linoleic acids (CLA), naturally found in dairy products and ruminant meat, are positional and geometric isomers (trans: t or cis: c) of linoleic acid, and have been widely reported to possess anti-tumoral activity against breast cancer both in vitro and in vivo. CLA isomer t9,t11 was recently proposed as an agonist of the transcriptional factor LXR, which is known for inducing genes implicated in cholesterol efflux. In this study, the growth inhibitory effect of three CLA isomers (c9,t11-CLA, t9,t11-CLA and t10,c12-CLA) was investigated on MCF-7 breast cancer cells, as well as their effect on LXR target genes. Our results revealed that t9,t11-CLA was the most efficient isomer by decreasing MCF-7 proliferation, inhibiting migration, and inducing apoptosis after 24h of treatment. t9,t11-CLA treatment led to an increase in the mRNA levels of LXR target genes involved in cholesterol efflux (ABCG1 and ARL7), as well as an increase of HMG-CoA-reductase which is the rate-limiting step of cholesterol biosynthesis. Interestingly, confocal microscopy analysis showed that t9,t11-CLA treatment remarkably reduced the intracellular and membrane-associated cholesterol levels. LXR activation through t9,t11-CLA isomer could lead to cholesterol cell deprivation by stimulating its efflux, which results in the inhibition of cell proliferation and stimulation of apoptosis.

摘要

共轭亚油酸(CLA)天然存在于乳制品和反刍动物肉中,是亚油酸的位置和立体异构体(反式:t 或顺式:c),已广泛报道其具有体外和体内抗乳腺癌的抗肿瘤活性。CLA 异构体 t9,t11 最近被提议为转录因子 LXR 的激动剂,该因子已知可诱导胆固醇流出所涉及的基因。在这项研究中,研究了三种 CLA 异构体(c9,t11-CLA、t9,t11-CLA 和 t10,c12-CLA)对 MCF-7 乳腺癌细胞的生长抑制作用,以及它们对 LXR 靶基因的影响。我们的结果表明,t9,t11-CLA 是最有效的异构体,可通过降低 MCF-7 增殖、抑制迁移和诱导细胞凋亡来治疗 24 小时。t9,t11-CLA 处理导致胆固醇流出(ABCG1 和 ARL7)涉及的 LXR 靶基因的 mRNA 水平增加,以及胆固醇生物合成限速步骤 HMG-CoA 还原酶增加。有趣的是,共聚焦显微镜分析表明,t9,t11-CLA 处理可显著降低细胞内和膜相关胆固醇水平。通过 t9,t11-CLA 异构体激活 LXR 可能通过刺激其流出导致胆固醇细胞剥夺,从而抑制细胞增殖并刺激细胞凋亡。

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