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Identification of WT1 as determinant of heptatocellular carcinoma and its inhibition by Chinese herbal medicine Salvia chinensis Benth and its active ingredient protocatechualdehyde

机译:WT1决定肝细胞癌的决定因素及其中药丹参及其活性成分原儿茶醛的抑制作用

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摘要

Candidates from Chinese herbal Medicine might be preferable in drug discovery as the abundant experiences of traditional use usually hint the clinical efficacy. In this study, we screened the anti-tumour effect of several commonly used Chinese herbal Medicines on human hepatocellular carcinoma cells (HCC). We identified that Salvia chinensia Benth. (Shijianchuan in Chinese, SJC) exhibited prominent in vitro inhibition of HCC cells and suppressed the orthotopic growth of HCC in the liver of mice and repressed the lung metastasis of tumour cells. Using a pathway-specific PCR array and Gene Ontology analysis, we identified that Wnt/β-catenin pathway was associated with the suppressive effect of SJC on HCC cell proliferation and cell cycle progression. SJC repressed transcription activity of Wnt/β-catenin pathway and reduced expression of β-catenin in GSK-3β-independent but promoter-specific transcription inhibition mechanism. The suppressive effect of SJC on β-catenin expression and its transcription activity was associated with Wilms’ tumor 1 (WT1) protein. WT1 was overexpressed in HCC tissues, and was negatively correlated to the overall survival of HCC patients. WT1 promoted proliferation and invasion of HCC cells, as well as β-catenin-dependent transcription activation of Wnt products, while knockdown of WT1 had the opposite effect. Docking experiment revealed that protocatechualdehyde (PCA) might be the active component of the herb. PCA suppressed transcription activity of Wnt/β-catenin pathway in WT1-dependent manner. Our study sheds light on the potential of PCA from commonly used anti-cancer Chinese herbal Medicine SJC as a lead compound targeting WT1 in the discovery of anti-HCC drugs.
机译:来自中草药的候选药物可能会更适合发现药物,因为传统使用的丰富经验通常暗示其临床疗效。在这项研究中,我们筛选了几种常用中草药​​对人肝癌细胞(HCC)的抗肿瘤作用。我们确定了丹参。 Shijianchuan(SJC),在体外对HCC细胞具有明显的抑制作用,并抑制了HCC在小鼠肝脏中的原位生长,并抑制了肿瘤细胞的肺转移。使用特定于途径的PCR阵列和基因本体分析,我们确定Wnt /β-catenin途径与SJC对HCC细胞增殖和细胞周期进程的抑制作用有关。 SJC抑制了Wnt /β-catenin途径的转录活性,并降低了GSK-3β依赖性但启动子特异性的转录抑制机制中β-catenin的表达。 SJC对β-catenin表达及其转录活性的抑制作用与Wilms的肿瘤1(WT1)蛋白有关。 WT1在肝癌组织中过表达,与肝癌患者的整体生存呈负相关。 WT1促进HCC细胞的增殖和侵袭,以及Wnt产物的β-catenin依赖性转录激活,而敲低WT1具有相反的作用。对接实验表明原儿茶醛(PCA)可能是该草药的活性成分。 PCA以WT1依赖性方式抑制Wnt /β-catenin途径的转录活性。我们的研究揭示了常用抗癌中草药SJC作为靶向WT1的先导化合物在抗HCC药物发现中的PCA潜力。

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