Liver Cancer Institute, Zhongshan Hospital, Shanghai, China.
Clinical Science Institute, Zhongshan Hospital, Shanghai, China.
Cell Biol Toxicol. 2016 Dec;32(6):499-511. doi: 10.1007/s10565-016-9351-z. Epub 2016 Jul 30.
A wide range of studies has demonstrated the potent anticancer activity of Chinese herbs. Here, we evaluated the anticancer activity and molecular mechanisms of Actinidia chinensis root extract (acRoots) on hepatocellular carcinoma (HCC). HepG2 HCC cells were treated with various concentrations of acRoots for 72 h and examined by mRNA expression profiling, revealing alterations in cellular immunity, inflammation, proliferation, cell cycle, and metabolic signaling responses. Further analysis of the altered genes in cellular immunity and inflammation gene clusters identified prostaglandin E receptor 3 (EP3) as a key regulator of gene expression in response to acRoots. Further analysis revealed inhibition of cell growth, migration, and invasion in HCC in response to acRoots, along with increased apoptosis due to downregulation of EP3 expression. Treatment with acRoots and EP3 antagonist L-798106 led to decreases in VEGF, EGFR, MMP2, and MMP9 expression in HCC cells, along with significant effects on growth, migration, invasion, and apoptosis; the effects were reversed/blocked by the EP3 agonist sulprostone. Taken together, these data clearly demonstrated that acRoots inhibit HCC cell invasion and metastasis via inhibition of EP3 expression, resulting in decreased activation of VEGF, EGFR, MMP2, and MMP9.
大量研究表明,中草药具有很强的抗癌活性。在这里,我们评估了猕猴桃根提取物(acRoots)对肝癌(HCC)的抗癌活性和分子机制。用不同浓度的 acRoots 处理 HepG2 HCC 细胞 72 h,通过 mRNA 表达谱分析,观察细胞免疫、炎症、增殖、细胞周期和代谢信号转导反应的变化。对细胞免疫和炎症基因簇中改变的基因进行进一步分析,发现前列腺素 E 受体 3(EP3)是响应 acRoots 表达的关键基因调控因子。进一步分析显示,acRoots 抑制 HCC 中的细胞生长、迁移和侵袭,同时由于 EP3 表达下调导致细胞凋亡增加。用 acRoots 和 EP3 拮抗剂 L-798106 处理 HCC 细胞,导致 VEGF、EGFR、MMP2 和 MMP9 表达下降,对生长、迁移、侵袭和凋亡有显著影响;EP3 激动剂舒前列素可逆转/阻断这些作用。总之,这些数据清楚地表明,acRoots 通过抑制 EP3 表达抑制 HCC 细胞的侵袭和转移,从而降低 VEGF、EGFR、MMP2 和 MMP9 的激活。