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首页> 外文期刊>Evidence-based complementary and alternative medicine: eCAM >PPTS Inhibits the TGF-β1-Induced Epithelial-Mesenchymal Transition in Human Colorectal Cancer SW480 Cells
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PPTS Inhibits the TGF-β1-Induced Epithelial-Mesenchymal Transition in Human Colorectal Cancer SW480 Cells

机译:PPT抑制人结直肠癌SW480细胞中TGF-β1诱导的上皮间过渡

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The current study investigates the inhibitory effects of Pulsatilla pentacyclic triterpenoid saponins extract (PPTS) on epithelial-mesenchymal transition (EMT) triggered by the transforming growth factor-β1 (TGF-β1) in human colorectal cancer SW480 cell line, further illustrates the possible mechanism of PPTS inhibition of growth and invasion from the perspective of EMT, and provides new theoretical support for the treatment of tumor by Chinese medicine. The SW480 cells were treated in groups: blank control, TGF-β1 (10?ng/mL), and varying concentrations of PPTS cotreated with TGF-β1-induced (10?ng/mL) groups. CCK8 was used to detect cell viability; transwell was applied to detect invasion ability, cell migration ability was also determined, ELISA and RT-qPCR were utilized for the determination of CYP3A, CYP2C9, CYP2C19, N-cadherin, and MMP-9 expression. Flow cytometry detection was applied to detect cell cycle and apoptosis. The results obtained have shown that PPTS can significantly inhibit the invasion and migration of tumors in SW480 cells and can also block the S phase in the cell cycle but may produce cytotoxicity in higher doses. The present research work provides substantial evidence that PPTS has a significant inhibitory effect on TGF-β1-induced EMT in SW480 cells and it also promotes apoptosis.
机译:目前的研究研究了普拉氏裂腾戊丙烯蛋白皂苷皂苷皂苷(PPT)对由转化生长因子-β1(TGF-β1)引发的上皮 - 间充质转换(EMT)的抑制作用进一步说明了可能的机制从EMT的角度抑制对生长和入侵的抑制,为中药治疗肿瘤的新理论支持。将SW480细胞分组处理:空白对照,TGF-β1(10→Ng / ml),以及用TGF-β1诱导的(10→Ng / mL)基团的不同浓度的PPT。 CCK8用于检测细胞活力;转发用于检测侵袭能力,还确定细胞迁移能力,ELISA和RT-QPCR用于测定CYP3A,CYP2C9,CYP2C19,N-钙粘蛋白和MMP-9表达。流式细胞术检测用于检测细胞周期和细胞凋亡。所得到的结果表明,PPT可以显着抑制SW480细胞中肿瘤的侵袭和迁移,并且还可以阻断细胞周期中的S相,但可能会产生更高剂量的细胞毒性。本研究工作提供了大量证据,即PPT对SW480细胞中TGF-β1诱导的EMT具有显着的抑制作用,并促进细胞凋亡。

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