首页> 美国卫生研究院文献>Oncology Letters >Treatment with the herbal formula Songyou Yin inhibits epithelial-mesenchymal transition in hepatocellular carcinoma through downregulation of TGF-β1 expression and inhibition of the SMAD2/3 signaling pathway
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Treatment with the herbal formula Songyou Yin inhibits epithelial-mesenchymal transition in hepatocellular carcinoma through downregulation of TGF-β1 expression and inhibition of the SMAD2/3 signaling pathway

机译:中药松油饮通过下调TGF-β1表达和抑制SMAD2 / 3信号通路抑制肝癌上皮-间质转化

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摘要

It was previously reported that treatment with the herbal formula Songyou Yin (SYY) may serve a role in attenuating epithelial-mesenchymal transition (EMT). In the present study, the effect of treatment with SYY on transforming growth factor-β1 (TGF-β1)-induced EMT was investigated and the potential underlying molecular mechanisms were evaluated. MHCC97H cells were pretreated with SYY for 4 weeks and subsequently named MHCC97HSYY cells. Simultaneously, MHCC97H cells were cultured for 4 weeks without SYY and used as a negative control. Western blot analysis and enzyme-linked immunosorbent assays demonstrated that treatment with SYY inhibited EMT-associated changes and TGF-β1 expression in MHCC97H cells. MHCC97H and MHCC97HSYY cells were treated with 10 ng/ml TGF-β1 to induce EMT. The results of the present study demonstrated that pretreatment with SYY markedly inhibited TGF-β1-induced morphological changes, and reversed the expression of the EMT markers E-cadherin and N-cadherin. In addition, expression levels of the TGF-β1 downstream proteins, phosphorylated mothers against decapentaplegic homologs (p-SMAD)2 and 3, were reduced. Transwell assays indicated that pretreatment with SYY inhibited TGF-β1-induced cancer cell invasion and migration. The results of the present study indicate that SYY inhibited EMT through attenuation of TGF-β1 expression, and downregulation of p-SMAD2 and 3.
机译:以前有报道称,用草药配方松油茵(SYY)进行治疗可能会减弱上皮-间质转化(EMT)。在本研究中,研究了SYY处理对转化生长因子-β1(TGF-β1)诱导的EMT的影响,并评估了潜在的潜在分子机制。 MHCC97H细胞用SYY预处理4周,随后命名为MHCC97HSYY细胞。同时,在没有SYY的情况下将MHCC97H细胞培养4周,并用作阴性对照。 Western印迹分析和酶联免疫吸附试验表明,SYY处理可抑制MHCC97H细胞中EMT相关变化和TGF-β1表达。用10ng / mlTGF-β1处理MHCC97H和MHCC97HSYY细胞以诱导EMT。本研究结果表明,用SYY预处理可显着抑制TGF-β1诱导的形态变化,并逆转EMT标记E-cadherin和N-cadherin的表达。此外,TGF-β1下游蛋白(针对去能力障碍同系物(p-SMAD)2和3)的磷酸化母亲的表达水平也降低了。 Transwell分析表明,SYY预处理可抑制TGF-β1诱导的癌细胞侵袭和迁移。本研究结果表明SYY通过减弱TGF-β1表达,下调p-SMAD2和3抑制EMT。

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