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首页> 外文期刊>European review for medical and pharmacological sciences. >Effects of lncRNA SNHG20 on proliferation and apoptosis of non-small cell lung cancer cells through Wnt/β-catenin signaling pathway
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Effects of lncRNA SNHG20 on proliferation and apoptosis of non-small cell lung cancer cells through Wnt/β-catenin signaling pathway

机译:LNCRNA SnHG20对通过Wnt /β-catenin信号通路的非小细胞肺癌细胞增殖和凋亡的影响

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摘要

OBJECTIVE: To investigate the influence of long non-coding ribonucleic acid (lncRNA) small nucleolar host gene 20 (SNHG20) on the proliferation and apoptosis of non-small cell lung cancer (NSCLC) cells through the Wnt/β-catenin signaling pathway. PATIENTS AND METHODS: The human NSCLC cells were cultured and lncRNA SNHG20 was inhibited using si-SNHG20 and overexpressed using SNHG20-OE. Then, flow cytometry was used to detect the apoptotic rate. The targets of lncRNA SNHG20 were detected via dual-luciferase reporter gene assay, and the changes in the protein level were detected via Western blotting. RESULTS: LncRNA SNHG20 was highly expressed in the cancer tissues and serum of patients with NSCLC. LncRNA SNHG20 could promote the proliferation and inhibit the apoptosis of NSCLC cells. LncRNA SNHG20 could bind to micro RNA (miR)-197 in a targeted manner. Besides, nuclear translocation of β-catenin was significantly enhanced after transfection of miR-197. After the down-regulation of miR-197 by small interfering RNA (siRNA), the key molecules TCF and LEF1 of the Wnt/β-catenin pathway were significantly down-regulated. CONCLUSIONS: LncRNA SNHG20 promotes the proliferation and inhibits the apoptosis of NSCLC cells by targeting miR-197 through the Wnt/β-catenin signaling pathway.
机译:目的:探讨长期非编码核糖核酸(LNCRNA)小核仁宿主基因20(SNHG20)对通过WNT /β-Catenin信号传导途径的非小细胞肺癌(NSCLC)细胞增殖和凋亡的影响。患者和方法:培养人NSCLC细胞,使用Si-SnHG20抑制LNCRNA SNHG20并使用SNHG20-OE过表达。然后,流式细胞术用于检测凋亡率。通过双荧光素酶报告基因测定检测LNCRNA SnHG20的靶标,通过蛋白质印迹检测蛋白质水平的变化。结果:LNCRNA SNHG20在NSCLC患者的癌症组织和血清中高度表达。 LNCRNA SNHG20可以促进增殖并抑制NSCLC细胞的凋亡。 LNCRNA SNHG20可以以靶向方式与微RNA(miR)-197结合。此外,MIR-197转染后,β-catenin的核转位显着提高。在通过小干扰RNA(siRNA)的miR-197的下调后,Wnt /β-catenin途径的关键分子Tcf和lef1显着下调。结论:LNCRNA SNHG20通过WNT /β-Catenin信号通路靶向MIR-197来促进增殖并抑制NSCLC细胞的凋亡。

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