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首页> 外文期刊>Evidence-based complementary and alternative medicine: eCAM >Qingjie Fuzheng Granule Inhibited the Migration and Invasion of Colorectal Cancer Cells by Regulating the lncRNA ANRIL/let-7a/TGF-β1/Smad Axis
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Qingjie Fuzheng Granule Inhibited the Migration and Invasion of Colorectal Cancer Cells by Regulating the lncRNA ANRIL/let-7a/TGF-β1/Smad Axis

机译:通过调节LNCRNA anril / Let-7a / TGF-β1/ Smad轴来抑制结肠直肠癌细胞的迁移和侵袭血清

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Qingjie Fuzheng granule (QFG) promotes cancer cell apoptosis and ameliorates intestinal mucosal damage caused by 5-fluorouracil. However, the antitumor role of QFG in colorectal cancer (CRC) progression remains unclear. In this study, the growth of HCT-8 and HCT116 cells incubated with various concentrations of QFG for 24 and 48?h was evaluated using MTT assays; their abilities of migration and invasion were investigated through wound healing and Transwell assays. The expression of lncRNA ANRIL, let-7a, and the TGF-β1/Smad signaling pathway components was assessed using real-time PCR and western blotting. The results elicited that QFG significantly suppressed the growth of HCT-8 and HCT116 cells; the half-maximal inhibitory concentrations (IC50) of QFG for HCT-8 and HCT116 cells for 48?h were 1.849 and 1.608?mg/mL, respectively. The abilities of wound healing, migration, and invasion of HCT-8 and HCT116 cells were dose-dependently decreased by QFG treatment for 24?h, respectively. QFG decreased the expression of lncRNA ANRIL, TGF-β1, phosphorylated (p)-Smad2/3, Smad4, and N-cadherin and upregulated the expression of let-7a in HCT-8 and HCT116 cells. Collectively, our data demonstrated that QFG inhibited the metastasis of CRC cells by regulating the lncRNA ANRIL/let-7a/TGF-β1/Smad axis, indicating that they might serve as an adjunctive medicine for CRC treatment.
机译:富正颗粒(QFG)促进癌细胞凋亡,改善5氟尿嘧啶引起的肠粘膜损伤。然而,QFG在结肠直肠癌(CRC)进展中的抗肿瘤作用仍不清楚。在该研究中,使用MTT测定评估了与各种浓度的QFG孵育的HCT-8和HCT116细胞的生长;通过伤口愈合和翻转测定来研究迁移和侵袭的能力。使用实时PCR和Western印迹评估LNCRNA anril,Let-7a和TGF-β1/ Smad信号传导途径组分的表达。结果引发了QFG显着抑制了HCT-8和HCT116细胞的生长; HCT-8和HCT116细胞的QFG的半最大抑制浓度(IC50)分别为1.849和1.608Ωmg/ ml。通过QFG处理分别对24μm的QFG处理剂量依赖性降低了HCT-8和HCT116细胞的伤口愈合,迁移和侵袭的能力。 QFG降低了LNCRNA anril,TGF-β1,磷酸化(P)-Smad2 / 3,Smad4和N-钙粘蛋白的表达,并在HCT-8和HCT116细胞中上调了Let-7a的表达。统称,我们的数据证明QFG通过调节LNCRNA anril / Let-7a / TGF-β1/ Smad轴来抑制CRC细胞的转移,表明它们可以作为CRC处理的辅助药物。

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