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首页> 外文期刊>European review for medical and pharmacological sciences. >Effects of circRNA_103993 on the proliferation and apoptosis of NSCLC cells through miR-1271/ERG signaling pathway
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Effects of circRNA_103993 on the proliferation and apoptosis of NSCLC cells through miR-1271/ERG signaling pathway

机译:Circrna_103993对通过MIR-1271 / ERG信号通路的NSCLC细胞增殖和凋亡的影响

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OBJECTIVE: Non-small cell lung cancer (NSCLC) accounts for more than 80% of lung cancer. CircRNA is a new type of non-coding RNA. CircRNA was found to be deeply involved in the regulation of NSCLC cells. However, the principle of CircRNA regulating NSCLC cells needs to be further explored. MATERIALS AND METHODS : The relative mRNA expression levels of CircRNA_103993, miR-1271 and ERG were detected by quantificational real-time polymerase chain reaction (qRT-PCR) in NSCLC cells and human bronchial epithelial cell line HBE. Cell proliferation was detected by the Cell Counting Kit (CCK8) when NSCLC cells were transfected with si-CircRNA_103993, si-NC, miR-1271 mimics, miR-NC, LV-ERG, respectively. The apoptotic rate of NSCLC cells was measured by apoptotic assay and flow Cytometry. The relative mRNA and protein expression levels of PCNA and caspase-3 were detected by Western blot and qRT-PCR. RESULTS: CircRNA_103993 and ERG were significantly up-regulated while miR-1271 was significantly down-regulated in NSCLC cells. Knockdown of CircRNA_103993 and high expression of miR-1271 significantly inhibited NSCLC cell proliferation and promoted apoptosis. The double luciferin report showed that CircRNA_103993 served as a sponge of miR-1271 and miR-1271 could directly target ERG in NSCLC cells. More importantly, low expression of CircRNA_103993 increased the expression level of miR-1271, and high expression of miR-1271 decreased the expression level of ERG. Further experiments showed that miR-1271 inhibitors reversed the effect of si-CircRNA_103993 on proliferation and apoptosis of NSCLC cells. However, miR-1271 mimics significantly promoted the effects of si-CircRNA_103993 on the proliferation and apoptosis. Moreover, LV-ERG reversed the effect of miR-1271 mimics on proliferation and apoptosis of NSCLC cells. However, si-ERG significantly promoted the effects of miR-1271 mimics on the proliferation and apoptosis. CONCLUSIONS: CircRNA_103993 was highly expressed in NSCLC cells. CircRNA_103993 regulated proliferation and apoptosis of NSCLC cells by acting as a sponge of miR-1271. The CircRNA_103993 /miR-1271/ ERG axis had an important effect on the proliferation and apoptosis of NSCLC cells. Therefore, CircRNA_103993 may be a target for treating lung cancer.
机译:目的:非小细胞肺癌(NSCLC)占肺癌的80%以上。 Circrna是一种新型的非编码RNA。发现CircrNA深入参与NSCLC细胞的调节。然而,需要进一步探索CircrNA调节NSCLC细胞的原理。材料和方法:通过在NSCLC细胞和人支气管上皮细胞系HBE中定量的实时聚合酶链反应(QRT-PCR)检测CircRNA_103993,miR-1271和ERG的相对mRNA表达水平。当用Si-circrna_103993,Si-Nc,miR-1271模拟,miR-nc,Lv-erg分别转染NSCLC细胞时,通过细胞计数试剂盒(CCK8)检测细胞增殖。通过凋亡测定和流式细胞术测量NSCLC细胞的凋亡率。通过Western印迹和QRT-PCR检测PCNA和Caspase-3的相对mRNA和蛋白表达水平。结果:CiRCRNA_103993和ERG显着上调,而MIR-1271在NSCLC细胞中显着下调。 Circrna_103993的敲低和MiR-1271的高表达显着抑制了NSCLC细胞增殖和促进凋亡。双荧光素报告显示CircRNA_103993用作miR-1271和miR-1271的海绵,可以直接靶向NSCLC细胞中的ERG。更重要的是,CiRCRNA_103993的低表达增加了miR-1271的表达水平,并且MiR-1271的高表达降低了ERG的表达水平。进一步的实验表明,miR-1271抑制剂逆转了Si-circrna_103993对Nsclc细胞增殖和凋亡的影响。然而,miR-1271模仿显着促进了Si-circrna_103993对增殖和细胞凋亡的影响。此外,LV-ERG逆转MIR-1271模拟对NSCLC细胞增殖和凋亡的影响。然而,Si-ERG显着促进了miR-1271模拟对增殖和凋亡的影响。结论:CiRcRNA_103993在NSCLC细胞中高度表达。 Circrna_103993通过作为miR-1271的海绵作用的调节NSCLC细胞的调节增殖和凋亡。 Circrna_103993 / miR-1271 / ERG轴对NSCLC细胞的增殖和凋亡产生了重要影响。因此,CircrNA_103993可以是治疗肺癌的靶标。

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