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Circ_0000003 通过 miR-338-3p/胰岛素受体底物 2 促进非小细胞肺癌细胞的增殖和转移。

Circ_0000003 promotes the proliferation and metastasis of non-small cell lung cancer cells via miR-338-3p/insulin receptor substrate 2.

机构信息

Department of Cardiothoracic Surgery, ZhuJiang Hospital of Southern Medical University, Guangzhou, Guangdong, China.

Department of Oncology, ZhuJiang Hospital of Southern Medical University, Guangzhou, Guangdong, China.

出版信息

Cell Cycle. 2019 Dec;18(24):3525-3539. doi: 10.1080/15384101.2019.1690883. Epub 2019 Nov 17.

Abstract

: Circular RNAs (circRNAs) play a pivotal regulatory role in a variety of tumors.Nevertheless, the detailed function of circ_0000003 in non-small cell lung cancer (NSCLC) and its regulatory mechanism remain elusive.: RT-PCR was carried out to detect the expressions of circ_0000003, miR-338-3p and insulin receptor substrate 2 (IRS2)in NSCLC tissues. Besides, western blot was done to monitor IRS2 expression in NSCLC cells. The correlation between circ_0000003 and clinicopathologic characteristics of NSCLC patients was analyzed as well.CCK8 and BrdUassays were used to monitor cell proliferation; flow cytometry was used to detect apoptosis; and transwell assay was conducted to detect its migration and invasion.Moreover, dual luciferase reporter gene assay was done to verify the targeting relationship between circ_0000003 and miR-338-3p.Additionally, the effect of circ_0000003 on the growth of NSCLC cells was evaluated by tumorigenesis assay in nude mice.: The expression of circ_0000003 was significantly high in NSCLC tissues and cell lines, and its high expression level was notably correlated with lymph node metastasis andTNM staging. experiments showed that overexpression of circ_0000003 facilitated the proliferation, migration, invasion and inhibited the apoptosis of NSCLC cells, while the knockdown of circ_0000003 had the opposite effect. experiments revealed that knockdown of circ_0000003 impeded tumor growth and metastasis. Further, the underlying mechanism showed that circ_0000003 functioned as endogenous competitive RNA and directly targeted miR-338-3p to positively regulated IRS2 expression.: Circ_0000003 promotes the proliferation and metastasis of NSCLC cells via modulating miR-338-3p/IRS2 axis.

摘要

环状 RNA(circRNAs)在多种肿瘤中发挥着关键的调节作用。然而,circ_0000003 在非小细胞肺癌(NSCLC)中的详细功能及其调节机制仍不清楚。

RT-PCR 用于检测 NSCLC 组织中 circ_0000003、miR-338-3p 和胰岛素受体底物 2(IRS2)的表达。此外,还通过 Western blot 监测 NSCLC 细胞中 IRS2 的表达。分析了 circ_0000003 与 NSCLC 患者临床病理特征的相关性。CCK8 和 BrdU 检测用于监测细胞增殖;流式细胞术用于检测细胞凋亡;Transwell 检测用于检测细胞迁移和侵袭。此外,还进行了双荧光素酶报告基因检测以验证 circ_0000003 与 miR-338-3p 之间的靶向关系。此外,通过裸鼠肿瘤发生实验评估了 circ_0000003 对 NSCLC 细胞生长的影响。

circ_0000003 在 NSCLC 组织和细胞系中表达明显升高,其高表达水平与淋巴结转移和 TNM 分期显著相关。实验表明,circ_0000003 的过表达促进了 NSCLC 细胞的增殖、迁移、侵袭,抑制了细胞凋亡,而 circ_0000003 的敲低则产生相反的效果。实验表明,circ_0000003 的敲低抑制了肿瘤的生长和转移。进一步的机制研究表明,circ_0000003 作为内源性竞争性 RNA,直接靶向 miR-338-3p 正向调控 IRS2 表达。

circ_0000003 通过调节 miR-338-3p/IRS2 轴促进 NSCLC 细胞的增殖和转移。

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