首页> 外文期刊>Journal of Ethnopharmacology: An Interdisciplinary Journal Devoted to Bioscientific Research on Indigenous Drugs >Total alkaloids of Tripterygium hypoglaucum (levl.) Hutch inhibits tumor growth both in vitro and in vivo
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Total alkaloids of Tripterygium hypoglaucum (levl.) Hutch inhibits tumor growth both in vitro and in vivo

机译:雷公藤总生物碱(levl。Hutch在体内外均抑制肿瘤生长)

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Ethnopharmacological relevance Tripterygium hypoglaucum (levl.) Hutch (Celastraceae) (THH) root is a traditional Chinese medicinal herb commonly used for treating autoimmune diseases and cancer. Alkaloid is one of the most bioactive components of THH extract. To evaluate the in vitro and in vivo antitumor properties of the total alkaloids of THH (THHta). Materials and methods THHta was extracted in pilot-scale. HCT116 cells were chose to establish human colon cancer xenograft model. The in vitro anti-tumor activity of THHta was tested by Cell malignant transformation test, Soft agar colony formation assay and MTT assay. The in vivo anti-tumor effect of THHta was confirmed by xenograft mouse model. THHta-induced apoptosis was examined by flow cytometry. The levels of apoptosis-related proteins were investigated by Western blot. Results TPA-induced cell transformation was significantly inhibited by THHta in JB6 Cl41 cells. THHta inhibits the growth of colon cancer cells in vitro in a significant dose-dependent manner. Compared to the control set, i.p. administration of THHta to xenograft mice significantly reduced both tumor weight and volume. Apoptosis induction of THHta was mediated by activation of caspase-3, PARP and inhibiting of Bcl-2, Bcl-xL and XIAP. Conclusion THHta was effective in inhibiting tumor growth both in vitro and in vivo at less toxic concentrations by inducing apoptosis which suggested it could be developed as a potential anticancer agent.
机译:民族药理学相关性雷公藤(荷香)的根是传统的中草药,通常用于治疗自身免疫性疾病和癌症。生物碱是THH提取物中最具生物活性的成分之一。为了评估THH(THHta)总生物碱的体外和体内抗肿瘤特性。材料和方法THHta以中试规模提取。选择HCT116细胞建立人结肠癌异种移植模型。通过细胞恶性转化试验,软琼脂菌落形成试验和MTT试验来检测THHta的体外抗肿瘤活性。通过异种移植小鼠模型证实了THHta的体内抗肿瘤作用。通过流式细胞术检查THHta诱导的凋亡。通过蛋白质印迹法研究凋亡相关蛋白的水平。结果THHta在JB6 Cl41细胞中显着抑制TPA诱导的细胞转化。 THHta以显着的剂量依赖性方式抑制体外结肠癌细胞的生长。与对照组相比对异种移植小鼠施用THHta显着降低了肿瘤的重量和体积。 THHta的凋亡诱导是通过激活caspase-3,PARP和抑制Bcl-2,Bcl-xL和XIAP介导的。结论THHta可通过诱导细胞凋亡而在较低的毒性浓度下有效地抑制肿瘤的体内外生长,提示其可能被开发为潜在的抗癌药。

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