Wang Xiu-Feng, Zhou Qian-Mei, Lu Yi-Yu, Zhang Hui, Huang Shuang, Su Shi-Bing
Shanghai University of Traditional Chinese Medicine, Research Center for Traditional Chinese Medicine Complexity System , Shanghai 201203 , China +86 215 132 3013 ;
Expert Opin Ther Targets. 2015 May;19(5):577-87. doi: 10.1517/14728222.2015.1012156. Epub 2015 Mar 31.
Radix Glycyrrhiza has been used in China for thousand years to treat cancer. However, focus on its tumor-suppressing mechanism has been concentrated on its effect on tumor cell growth and apoptosis.
With the aid of a panel of human breast cancer cell lines, we reveal that glycyrrhetinic acid (GA), a major component of Radix Glycyrrhiza, is actually a significantly more potent agent to suppress invasion than cell survival.
GA effectively inhibits breast cancer cell MMP-2/MMP-9 expression; GA-induced reduction in the MMP-2/9 expression is apparently mediated by GA's ability to specifically inhibit the p38 MAPK activity and its downstream AP1 activation. Moreover, we show that GA down regulates the levels of Fra-1 and c-Jun, two main components of AP1 transcription complex in invasive breast cancer cells and that AP1-specific inhibitor abrogates breast cancer cell invasion. These results suggest that GA impairs the p38 MAPK-AP1 signaling axis, leading to the repression of breast cancer cell invasion. Finally, we demonstrate that GA effectively suppresses breast tumor outgrowth and pulmonary metastasis without causing animal weight loss or eliciting liver/kidney toxicity to the recipient animals.
This study indicates that GA represents a good candidate compound for the potential development of therapeutic drug.
甘草在中国已被用于治疗癌症达数千年之久。然而,对其抑癌机制的关注主要集中在对肿瘤细胞生长和凋亡的影响上。
借助一组人乳腺癌细胞系,我们发现甘草的主要成分甘草次酸(GA)实际上是一种比抑制细胞存活更有效的抑制侵袭的药物。
GA有效抑制乳腺癌细胞MMP - 2/MMP - 9的表达;GA诱导的MMP - 2/9表达降低显然是由GA特异性抑制p38丝裂原活化蛋白激酶(MAPK)活性及其下游AP1激活的能力介导的。此外,我们表明GA下调侵袭性乳腺癌细胞中AP1转录复合物的两个主要成分Fra - 1和c - Jun的水平,并且AP1特异性抑制剂可消除乳腺癌细胞的侵袭。这些结果表明GA损害p38 MAPK - AP1信号轴,导致乳腺癌细胞侵袭受到抑制。最后,我们证明GA有效抑制乳腺肿瘤生长和肺转移,而不会导致动物体重减轻或对受体动物引发肝/肾毒性。
本研究表明GA是治疗药物潜在开发的良好候选化合物。