School of Medical Laboratory and Biotechnology, Chung Shan Medical University, Taichung, Taiwan.
Br J Pharmacol. 2011 Jan;162(1):237-54. doi: 10.1111/j.1476-5381.2010.01022.x.
Protocatechuic acid (PCA) is plentiful in edible fruits and vegetables and is thus one anti-oxidative component of normal human diets. However, the molecular mechanisms involved in the chemopreventive activity of PCA are poorly understood. Here, we investigated the mechanism(s) underlying the anti-metastatic potential of PCA.
We used AGS cells in a wound healing model and Boyden chamber assays in vitro and injection of B16/F10 melanoma cells in mice (metastasis model in vivo) to analyse the effect of PCA on cancer cell invasion and metastasis. The activities and expression of molecular proteins were measured by zymographic assay, real-time RT-PCR and Western blotting.
PCA inhibited cell migration and invasion at non-cytotoxic concentrations. Decreased expression of matrix metalloproteinase (MMP)-2 and a coincident increase in tissue inhibitor of MMP followed treatment with PCA. The PCA-inhibited MMP-2 activity and expression was accompanied by inactivation of NF-κB. All these effects of PCA could be mediated via the RhoB/ protein kinase Cε (PKCε) and Ras/Akt cascade pathways, as demonstrated by inhibition of PKCε and transfection of PKCε siRNA and ras overexpression vector. Finally, PCA inhibited metastasis of B16/F10 melanoma cells to the liver in mice.
Our data imply that PCA down-regulated the Ras/Akt/NF-κB pathway by targeting RhoB activation, which in turn led to a reduction of MMP-mediated cellular events in cancer cells and provides a new mechanism for the anti-cancer activity of PCA.
原儿茶酸(PCA)在食用水果和蔬菜中含量丰富,是正常人体饮食中抗氧化成分之一。然而,PCA 发挥化学预防作用的分子机制还知之甚少。本研究旨在探讨 PCA 抗转移作用的潜在机制。
我们在体外划痕愈合模型和 Boyden 室测定中使用 AGS 细胞,在小鼠中注射 B16/F10 黑色素瘤细胞(体内转移模型)来分析 PCA 对癌细胞侵袭和转移的影响。通过明胶酶谱分析、实时 RT-PCR 和 Western blot 来检测分子蛋白的活性和表达。
PCA 在非细胞毒性浓度下抑制细胞迁移和侵袭。与 PCA 处理后 MMP-2 表达降低相一致的是,基质金属蛋白酶抑制剂(TIMP)表达增加。PCA 抑制 MMP-2 活性和表达伴随着 NF-κB 的失活。所有这些 PCA 的作用都可以通过 RhoB/蛋白激酶 Cε(PKCε)和 Ras/Akt 级联途径介导,如 PKCε 抑制和 PKCε siRNA 转染以及 ras 过表达载体的抑制作用所证明。最后,PCA 抑制了 B16/F10 黑色素瘤细胞在小鼠肝脏的转移。
我们的数据表明,PCA 通过靶向 RhoB 激活下调 Ras/Akt/NF-κB 通路,进而减少 MMP 介导的癌细胞中的细胞事件,为 PCA 的抗癌活性提供了新的机制。