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首页> 外文期刊>RSC Advances >Aqueous extract of Sanguisorba officinalis blocks the Wnt/β-catenin signaling pathway in colorectal cancer cells
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Aqueous extract of Sanguisorba officinalis blocks the Wnt/β-catenin signaling pathway in colorectal cancer cells

机译:Sanguisorba officinalis的水提物阻断大肠癌细胞中的Wnt /β-catenin信号通路

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Sanguisorba officinalis (the Chinese name is DiYu, DY) exerts significant anti-proliferative activities against colorectal cancer (CRC) cells. Since most of CRC result from the aberrant activation of the Wnt/β-catenin signaling pathway, inhibitors of the Wnt pathway are considered as promising anti-CRC agents. This study aimed to investigate whether DY could be a potential herbal Wnt inhibitor, and the bioactive constituents and underlying molecular mechanisms for DY's inhibiting activities would be studied as well. Accordingly, the inhibitory activities of DY and its main components against the Wnt pathway were assessed using the single-luciferase reporter assay based on HEK293 cells. Additionally, the levels of key Wnt-related genes or proteins were measured to verify the inhibitory effects on the Wnt pathway of CRC cells. Finally, the underlying mechanisms accounting for the efficacy of candidate drugs were explored by the transcriptomic study. Results show that DY and its tannins (RZ), and saponins (ZG) significantly inhibited the Wnt pathway of HEK293 cells activated by wnt3a. However, their respective constituents were not effective as expected. Additionally, DY and RZ prominently down-regulated the levels of β-catenin and Wnt-targeted genes including Axin2 , c-Myc or CyclinD1 of three CRC cells. Transcriptomic profiling study suggests that the down-regulation of the mRNA levels of Wnt-related genes such as LPAR6 may be associated with the inhibitory effects of DY and RZ on the Wnt pathway of HT29 cells. Therefore, our studies first uncovered the blocking activity of DY on the Wnt pathway, providing evidence for the rationale of developing Wnt inhibitors from DY as anti-CRC agents.
机译:Sanguisorba officinalis(中文名称为DiYu,DY)对结直肠癌细胞(CRC)具有重要的抗增殖活性。由于大多数CRC是由Wnt /β-catenin信号通路的异常激活引起的,因此Wnt通路的抑制剂被认为是有前途的抗CRC药物。这项研究旨在调查DY是否可能是潜在的草药Wnt抑制剂,并且还将研究DY抑制活性的生物活性成分和潜在分子机制。因此,使用基于HEK293细胞的单荧光素酶报告基因测定法评估了DY及其主要成分对Wnt途径的抑制活性。另外,测量关键的Wnt相关基因或蛋白质的水平以验证对CRC细胞的Wnt途径的抑制作用。最后,通过转录组研究探索了解释候选药物功效的潜在机制。结果表明,DY及其单宁(RZ)和皂苷(ZG)显着抑制了wnt3a激活的HEK293细胞的Wnt途径。但是,它们各自的组成部分并没有达到预期的效果。此外,DY和RZ显着下调了三个CRC细胞的β-catenin和Wnt靶向基因(包括Axin2,c-Myc或CyclinD1)的水平。转录组分析研究表明,Wnt相关基因(如LPAR6)mRNA水平的下调可能与DY和RZ对HT29细胞Wnt途径的抑制作用有关。因此,我们的研究首先揭示了DY对Wnt途径的阻断活性,为从DY开发Wnt抑制剂作为抗CRC药物的原理提供了证据。

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