Huang Shiu-Chen, Ho Chi-Tang, Lin-Shiau Shoei-Yn, Lin Jen-Kun
Institute of Biochemistry and Molecular Biology, College of Medicine, National Taiwan University, No. 1, Section 1, Jen-ai Road Taipei 10018, Taiwan.
Biochem Pharmacol. 2005 Jan 15;69(2):221-32. doi: 10.1016/j.bcp.2004.09.019. Epub 2004 Nov 23.
Carnosol, a constant constituent of Rosmarinus officinalis extracts, is a phenolic diterpene shown to have antioxidant and anticarcinogen properties. In our studies, carnosol inhibited the invasion of highly metastatic mouse melanoma B16/F10 cells in vitro. First, the antimetastatic potentials of carnosol were examined by soft agar colony formation assay. Second, carnosol dose-dependently inhibited B16/F10 cell migration and invasion by in vitro transwell assay. Third, the decreasing activity of metalloproteinase was observed by zymographic assay. The result revealed that the treatment of carnosol could diminish the activity of MMP-9 more than MMP-2. Next, we analyzed the amounts of MMP-9 and MMP-2 proteins in the cells. The data indicated MMP-9 protein was also suppressed by carnosol in the same manner. In accordance with the above data, the results of reverse transcriptase polymerase chain reaction (RT-PCR) analysis showed a reduced level of MMP-9 mRNA. Furthermore, carnosol significantly inhibited the tyrosine phosphorylation of extracellular signal-regulated kinase (ERK) 1/2, AKT, p38, JNK and inhibition of activation of transcription factors NFkappa-B and c-Jun. These results lead us to conclude that carnosol could restrict the invasive ability of B16/F10 mouse melanoma cells by reducing MMP-9 expression and activity through suppressing (ERK) 1/2, AKT, p38, and JNK signaling pathway and inhibition of NF-kappaB and AP-1 binding activity. Taken together, these results indicate that carnosol targets MMP-mediated cellular events in cancer cells and provides a new mechanism for its anticancer activity.
鼠尾草酸是迷迭香提取物中的一种常量成分,是一种酚类二萜,具有抗氧化和抗癌特性。在我们的研究中,鼠尾草酸在体外抑制了高转移性小鼠黑色素瘤B16/F10细胞的侵袭。首先,通过软琼脂集落形成试验检测了鼠尾草酸的抗转移潜力。其次,通过体外Transwell试验,鼠尾草酸剂量依赖性地抑制了B16/F10细胞的迁移和侵袭。第三,通过酶谱分析观察到金属蛋白酶活性降低。结果显示,鼠尾草酸处理对MMP-9活性的降低作用比对MMP-2的作用更大。接下来,我们分析了细胞中MMP-9和MMP-2蛋白的含量。数据表明,鼠尾草酸也以同样的方式抑制了MMP-9蛋白。根据上述数据,逆转录聚合酶链反应(RT-PCR)分析结果显示MMP-9 mRNA水平降低。此外,鼠尾草酸显著抑制细胞外信号调节激酶(ERK)1/2、AKT、p38、JNK的酪氨酸磷酸化,并抑制转录因子NFκB和c-Jun的激活。这些结果使我们得出结论,鼠尾草酸可通过抑制(ERK)1/2、AKT、p38和JNK信号通路以及抑制NF-κB和AP-1结合活性,降低MMP-9的表达和活性,从而限制B16/F10小鼠黑色素瘤细胞的侵袭能力。综上所述,这些结果表明鼠尾草酸靶向癌细胞中MMP介导的细胞事件,并为其抗癌活性提供了一种新机制。