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梓醇苷 II 对肝癌细胞具有抗增殖和抗转移作用。

Ziyuglycoside II exerts antiproliferative and antimetastasis effects on hepatocellular carcinoma cells.

机构信息

Department of Basic Medicine and Biomedical Engineering, School of Stomatology and Medicine, Foshan University, Foshan, Guangdong, China.

出版信息

Anticancer Drugs. 2020 Sep;31(8):819-827. doi: 10.1097/CAD.0000000000000918.

DOI:10.1097/CAD.0000000000000918
PMID:32097137
Abstract

Hepatocellular carcinoma (HCC) is a leading cause of cancer-related death worldwide. Phytochemicals are important candidates for developing anticancer agents. Ziyuglycoside II is a major active compound of Sanguisorba officinalis, which exhibits antiproliferation activity in several cancers; however, its action in HCC remains unknown. In this study, we investigated the antitumor activity of ziyuglycoside II against HCC and explored the potential mechanisms. We found that ziyuglycoside II exerts significant inhibitory effects on the viability and clonogenic activity of HCC cells. The proliferation repression mediated by ziyuglycoside II was mainly due to increased apoptosis and reactive oxygen species accumulation, as well as a G0/G1 phase cell-cycle arrest. Additionally, ziyuglycoside II markedly impaired HCC cell migration and invasion, two important steps during metastasis, and these suppressive effects may be attributed to the downregulation of matrix metalloproteinases MMP2 and MMP9 expression. Moreover, ziyuglycoside II blocked the epidermal growth factor receptor/nuclear factor kappa-B (EGFR/NF-kB) signaling, which may contribute to its anticancer activity. Taken together, our findings reveal antiproliferative and antimetastasis activities of ziyuglycoside II in HCC cells, implying that ziyuglycoside II might be a promising candidate for the development of novel anti-HCC drugs.

摘要

肝细胞癌(HCC)是全球癌症相关死亡的主要原因。植物化学物质是开发抗癌药物的重要候选物。紫珠苷 II 是地榆中的一种主要活性化合物,它在几种癌症中表现出抗增殖活性;然而,其在 HCC 中的作用尚不清楚。在这项研究中,我们研究了紫珠苷 II 对 HCC 的抗肿瘤活性,并探讨了其潜在机制。我们发现紫珠苷 II 对 HCC 细胞的活力和克隆形成活性具有显著的抑制作用。紫珠苷 II 介导的增殖抑制主要归因于细胞凋亡和活性氧积累增加,以及 G0/G1 期细胞周期停滞。此外,紫珠苷 II 显著抑制 HCC 细胞迁移和侵袭,这是转移过程中的两个重要步骤,这些抑制作用可能归因于基质金属蛋白酶 MMP2 和 MMP9 表达的下调。此外,紫珠苷 II 阻断了表皮生长因子受体/核因子 kappa-B(EGFR/NF-kB)信号通路,这可能有助于其抗癌活性。综上所述,我们的研究结果揭示了紫珠苷 II 在 HCC 细胞中的增殖抑制和抗转移活性,表明紫珠苷 II 可能是开发新型抗 HCC 药物的有前途的候选物。

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