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Identification of the tumor-suppressive function of circular RNA FOXO3 in non-small cell lung cancer through sponging miR-155

机译:通过海绵MiR-155鉴定非小细胞肺癌圆形RNA FoxO3的肿瘤抑制功能

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摘要

Circular RNAs (circRNAs) are a class of endogenous noncoding RNAs that have been demonstrated to be potential regulators in the development and progression of various types of human cancer. However, little is known about their roles in cancer initiation and progression, particular in non-small cell lung cancer (NSCLC). In the present study, the expression level of circRNA-forkhead box O3 class (FOXO3) in NSCLC specimens was determined and its functional role was investigated in NSCLC cells. By performing Taq-man based RT-qPCR, it was identified that circRNA-FOXO3 was downregulated in NSCLC tissues and cell lines. Receiver operating curve analysis indicated that circRNA-FOXO3 had a relatively higher diagnostic accuracy. The functional relevance was further examined by biological assays. circRNA-FOXO3 significantly promoted the ability of cell proliferation, migration and invasion of NSCLC cells. The linear isomer of circRNA-FOXO3, FOXO3 gene, was identified as a downstream target. RNA immunoprecipitation indicated that circRNA-FOXO3 sequestering miR-155, which further promoted linear FOXO3 expression. In addition, gain and loss functional assays indicated that circRNA-FOXO3 served an anti-oncogenic role through sequestering miR-155 and enhancing FOXO3 expression. These results suggest that circRNA-FOXO3 is a tumor-suppressor in NSCLC and may serve as a promising therapeutic target. Therefore, restoration of circRNA-FOXO3 expression could be a future approach to develop a novel treatment strategy.
机译:圆形RNA(Circrna)是一类内源性非编码RNA,已被证明是各种类型人类癌症的开发和进展中的潜在调节因素。然而,对于癌症起始和进展的作用很少,特别是非小细胞肺癌(NSCLC)。在本研究中,测定了NSCLC样本中的Circrna-Forkhead盒O3类(FoxO3)的表达水平,并在NSCLC细胞中研究了其功能作用。通过进行基于Taq-man的RT-QPCR,鉴定了CircrNA-FoxO3在NSCLC组织和细胞系中下调。接收器操作曲线分析表明Circrna-FoxO3具有相对较高的诊断精度。通过生物学测定进一步检查功能相关性。 Circrna-FoxO3显着促进了细胞增殖,迁移和NSCLC细胞侵袭的能力。 Circrna-FoxO3,FoxO3基因的线性异构体被鉴定为下游靶标。 RNA免疫沉淀表明CircRNA-FoxO3螯合miR-155,其进一步促进了线性FoxO3表达。此外,增益和损失功能测定表明,Circrna-FoxO3通过螯合miR-155并增强FoxO 3表达来提供抗癌作用。这些结果表明Circrna-FoxO3是NSCLC中的肿瘤抑制剂,可用作有前途的治疗靶标。因此,Circrna-Foxo3表达的恢复可能是开发新型治疗策略的未来方法。

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