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