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共轭亚油酸 t,t 型对 12-O-十四烷酰佛波醇-13-醋酸酯诱导的人乳腺上皮 MCF-10A 细胞缝隙连接细胞间通讯抑制的预防作用。

Preventive effect of t,t-conjugated linoleic acid on 12-O-tetradecanoylphorbol-13-acetate-induced inhibition of gap junctional intercellular communication in human mammary epithelial MCF-10A cells.

机构信息

Division of Applied Life Science (BK21 Program), Graduate School, Gyeongsang National University, Jinju, Republic of Korea.

出版信息

J Agric Food Chem. 2011 Apr 27;59(8):4164-70. doi: 10.1021/jf1046909. Epub 2011 Mar 10.

Abstract

The anti-tumor promotional effects of t9,t11-conjugated linoleic acid (t9,t11-CLA) and t10,t12-CLA were evaluated on the 12-O-tetradecanoylphorbol-13-acetate (TPA)-induced inhibition of gap junctional intercellular communication (GJIC) in the human mammary epithelial cell line MCF-10A. The results were compared to those obtained from c9,t11-CLA, which is a more effective anti-tumor promoter on TPA-induced GJIC inhibition in MCF-10A cells than t10,c12-CLA. Cells were treated with 20 μM t9,t11-CLA, t10,t12-CLA, or c9,t11-CLA for 24 h followed by 60 nM TPA for 1 h. Both t9,t11-CLA and t10,t12-CLA equally protected MCF-10A cells from TPA-induced inhibition of GJIC with inferior efficacy to c9,t11-CLA.The protection was due to the ameliorated phosphorylation of connexin43 via suppression of extracellular signal-regulated kinases (ERK1/2) activation. Suppression of TPA-induced reactive oxygen species (ROS) generation by t9,t11-CLA and t10,t12-CLA was less effective, relative to c9,t11-CLA. The results suggest that the anti-promotional activities of t9,t11-CLA and t10,t12-CLA are equal but less potent than c9,t11-CLA in TPA-treated MCF-10A cells. The activity might be mediated by the attenuation of ROS production in MCF-10A cells by preventing the downregulation of GJIC during the cancer promotion stage.

摘要

我们评价了 t9,t11-共轭亚油酸(t9,t11-CLA)和 t10,t12-CLA 的抗肿瘤促进作用,以及它们对人乳腺上皮细胞 MCF-10A 中 12-O-十四烷酰佛波醇-13-乙酸酯(TPA)诱导的间隙连接细胞间通讯(GJIC)抑制的影响。我们将结果与 c9,t11-CLA 进行了比较,c9,t11-CLA 是 MCF-10A 细胞中比 t10,c12-CLA 更有效的 TPA 诱导 GJIC 抑制的抗肿瘤促进剂。细胞用 20 μM t9,t11-CLA、t10,t12-CLA 或 c9,t11-CLA 处理 24 小时,然后用 60 nM TPA 处理 1 小时。t9,t11-CLA 和 t10,t12-CLA 均能同等保护 MCF-10A 细胞免受 TPA 诱导的 GJIC 抑制,其效果不如 c9,t11-CLA。这种保护是由于细胞连接蛋白 43 的磷酸化通过抑制细胞外信号调节激酶(ERK1/2)的激活而得到改善。t9,t11-CLA 和 t10,t12-CLA 抑制 TPA 诱导的活性氧(ROS)生成的效果不如 c9,t11-CLA,相对较弱。结果表明,t9,t11-CLA 和 t10,t12-CLA 的抗促进活性在 TPA 处理的 MCF-10A 细胞中与 c9,t11-CLA 相等,但效果较弱。该活性可能是通过在癌症促进阶段防止 GJIC 下调来减轻 MCF-10A 细胞中 ROS 产生而介导的。

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