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Polyphyllin I suppresses the formation of vasculogenic mimicry via Twist1/VE-cadherin pathway

机译:Polyphyllin I通过Twist1 / Ve-Cadherin途径抑制血管原性模拟的形成

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Vasculogenic mimicry (VM) is a functional microcirculation pattern formed by aggressive tumor cells and is related to the metastasis and poor prognosis of many cancer types, including hepatocellular carcinoma (HCC). Thus far, no effective drugs have been developed to target VM. In this study, patients with liver cancer exhibited reduced VM in tumor tissues after treatment with Rhizoma Paridis. Polyphyllin I (PPI), which is the main component of Rhizoma Paridis, inhibited VM formation in HCC lines and transplanted hepatocellular carcinoma cells. Molecular mechanism analysis showed that PPI impaired VM formation by blocking the PI3k-Akt-Twist1-VE-cadherin pathway. PPI also displayed dual effects on Twist1 by inhibiting the transcriptional activation of the Twist1 promoter and interfering with the ability of Twist1 to bind to the promoter of VE-cadherin, resulting in VM blocking. This study is the first to report on the clinical application of the VM inhibitor. Results may contribute to the development of novel anti-VM drugs in clinical therapeutics.
机译:血管原性模拟(VM)是通过侵蚀性肿瘤细胞形成的功能微循环图案,与许多癌症类型的转移和预后差,包括肝细胞癌(HCC)有关。到目前为止,没有开发有效的药物对目标VM。在这项研究中,肝癌患者在用根茎治疗后肿瘤组织中的VM减少。 Polyphyllin I(PPI),其是Rhizoma Paricis的主要成分,抑制HCC线和移植肝癌细胞中的VM形成。分子机制分析表明,通过阻断PI3K-AKT-TWICK1-VE-CADHERIN途径,PPI受损的VM形成。通过抑制Twist1启动子的转录激活并干扰Twist1与Ve-Cadherin的启动子结合的能力,PPI对Twistr的效果显示了双重影响,导致VM阻断。本研究是第一个报告VM抑制剂的临床应用的报告。结果可能有助于开发新型抗民族药物在临床治疗中的发展。

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