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首页> 外文期刊>Molecular medicine reports >Astragalus polysaccharide inhibits breast cancer cell migration and invasion by regulating epithelial-mesenchymal transition via the Wnt/beta-catenin signaling pathway
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Astragalus polysaccharide inhibits breast cancer cell migration and invasion by regulating epithelial-mesenchymal transition via the Wnt/beta-catenin signaling pathway

机译:黄芪多糖通过通过WNT /β-连环蛋白信号通路调节上皮 - 间充质转换来抑制乳腺癌细胞迁移和侵袭

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摘要

Epithelial-mesenchymal transition (EMT) serves an important role in tumor migration and invasion. Astragalus polysaccharide (APS), which is the main component of the traditional Chinese medicine Astragalus membranaceus, has been identified to display an antitumor effect. However, the effects and mechanisms of APS during breast cancer migration and invasion are not completely understood. The present study investigated whether APS inhibited breast cancer migration and invasion by modulating the EMT pathway. An MTT assay and a Ki67 immunofluorescence staining assay demonstrated that APS inhibited the proliferation of breast cancer cells. The results of the wound healing and Transwell Matrigel invasion assays suggested that APS decreased the migration and invasion of breast cancer cells. The western blotting and immunofluorescence analyses further demonstrated that APS had a regulatory effect on EMT-related molecules. APS decreased the expression levels of Snail and vimentin, but increased E-cadherin expression. APS also downregulated Wnt1, beta-catenin and downstream target expression. Additionally, the present results suggested that APS decreased the proliferation, and EMT-mediated migration and invasion of cells by inhibiting the Wnt/beta-catenin signaling pathway. The present study suggested that APS may serve as a promising therapeutic agent for breast cancer.
机译:上皮 - 间充质转换(EMT)在肿瘤迁移和侵袭方面发挥着重要作用。 Astragalus多糖(APS)是中医阿斯塔哥州膜的主要成分,已被识别出现抗肿瘤效应。然而,乳腺癌迁移和入侵期间APS的效果和机制并不完全理解。本研究研究了APS是否抑制EMT途径抑制乳腺癌迁移和侵袭。 MTT测定和KI67免疫荧光染色测定证明APS抑制乳腺癌细胞的增殖。伤口愈合和Transwell Matrigel侵袭测定的结果表明,APS降低了乳腺癌细胞的迁移和侵袭。蛋白质印迹和免疫荧光分析进一步证明APS对EMT相关分子具有调节作用。 APS减少了蜗牛和蜗杆蛋白的表达水平,而是增加了e-cadherin表达。 APS还下调WNT1,β-连环蛋白和下游靶表达。另外,本结果表明APS通过抑制WNT /β-连环蛋白信号传导途径来降低增殖,EMT介导的细胞迁移和侵袭细胞。本研究表明,APS可以作为乳腺癌的有希望的治疗剂。

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