首页> 美国卫生研究院文献>Evidence-based Complementary and Alternative Medicine : eCAM >Asparagus Polysaccharide Suppresses the Migration Invasion and Angiogenesis of Hepatocellular Carcinoma Cells Partly by Targeting the HIF-1α/VEGF Signalling Pathway In Vitro
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Asparagus Polysaccharide Suppresses the Migration Invasion and Angiogenesis of Hepatocellular Carcinoma Cells Partly by Targeting the HIF-1α/VEGF Signalling Pathway In Vitro

机译:芦笋多糖部分抑制HIF-1α/ VEGF信号通路体外抑制肝癌细胞的迁移侵袭和血管生成

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摘要

Hypoxia-inducible factor-1α (HIF-1α) plays a key role by triggering the transcriptional activation of a number of genes involved in migration, invasion, and angiogenesis in hepatocellular carcinoma (HCC). Thus, suppressing tumour growth by targeting the HIF-1α/VEGF signalling pathway represents a promising strategy for the treatment of HCC. In our previous studies, we found that asparagus polysaccharide (ASP) suppressed the proliferation and promoted the apoptosis of HCC cells both in vivo and in vitro. To further explore the potential mechanisms of the antitumor effects of ASP in HCC, we investigated effects of ASP on the migration, invasion, and angiogenesis of HCC cells (SK-Hep1 and Hep-3B) using an in vitro experimental model. First, we found that ASP effectively suppressed the proliferation of the SK-Hep1 and Hep-3B cells but did not cause significant cytotoxicity in normal liver cells (L-O2). Then, we found that ASP inhibited the migration and invasion of the SK-Hep1 and Hep-3B cells and HCC cells-induced angiogenesis of human umbilical vein endothelial cells in a concentration-dependent manner. Mechanistic studies revealed that the inhibition of migration, invasion, and angiogenesis by ASP in the SK-Hep1 and Hep-3B cells might occur via the downregulation of HIF-1α/VEGF signalling pathway. Finally, our results also showed that the inhibition of HIF-1α by ASP may be mediated through the downregulation of the phosphorylation levels of AKT, mTOR, and ERK. In conclusion, our results suggest that ASP suppresses the migration, invasion, and angiogenesis of HCC cells partly via inhibiting the HIF-1α/VEGF signalling pathway.
机译:缺氧诱导因子-1α(HIF-1α)通过触发肝细胞癌(HCC)中许多与迁移,侵袭和血管生成有关的基因的转录激活而发挥关键作用。因此,通过靶向HIF-1α/ VEGF信号传导途径抑制肿瘤生长代表了治疗HCC的有前途的策略。在我们以前的研究中,我们发现芦笋多糖(ASP)在体内和体外均可抑制HCC细胞的增殖并促进其凋亡。为了进一步探讨ASP在HCC中抗肿瘤作用的潜在机制,我们使用体外实验模型研究了ASP对HCC细胞(SK-Hep1和Hep-3B)迁移,侵袭和血管生成的影响。首先,我们发现ASP有效抑制SK-Hep1和Hep-3B细胞的增殖,但在正常肝细胞(L-O2)中并未引起明显的细胞毒性。然后,我们发现ASP以浓度依赖的方式抑制了SK-Hep1和Hep-3B细胞的迁移和侵袭以及HCC细胞诱导的人脐静脉内皮细胞的血管生成。机理研究表明,ASP对SK-Hep1和Hep-3B细胞迁移,侵袭和血管生成的抑制作用可能是通过下调HIF-1α/ VEGF信号通路来实现的。最后,我们的结果还表明,ASP对HIF-1α的抑制作用可能是通过下调AKT,mTOR和ERK的磷酸化水平来介导的。总之,我们的结果表明ASP通过抑制HIF-1α/ VEGF信号通路部分抑制了HCC细胞的迁移,侵袭和血管生成。

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