Wang Qi, Ling Shengying, Lv Jia, Wu Lina
Department of General Practice, Renji Hospital, Shanghai JiaoTong University School of Medicine, Shanghai, China.
Department of Obstetrics and Gynecology, Shanghai Fourth People's Hospital, School of Medicine, Tongji University, Shanghai 200434, China.
Anal Cell Pathol (Amst). 2025 Jan 4;2025:5595692. doi: 10.1155/ancp/5595692. eCollection 2025.
Circular RNAs (circRNAs), covalently closed single-stranded RNAs, have been implicated in cancer progression. A previous investigation revealed that circ-ZEB1 is expressed abnormally in liver cancer. However, the roles of circ-ZEB1 in non-small cell lung cancer (NSCLC) are unknown. In this study, we used fluorescence in situ hybridization (FISH) and RT-qPCR to study circ-ZEB1 expression in NSCLC cells and tissues. A luciferase reporter assay was performed to validate downstream targets of circ-ZEB1. Transwell migration, 5-ethynyl-20-deoxyuridine (EdU), and cell counting kit-8 (CCK8) assays were performed to assess proliferation and migration. In vivo metastasis and tumorigenesis assays were also performed to investigate circ-ZEB1 functions during NSCLC. Our results showed that circ-ZEB1 expression was increased in NSCLC tissues and cells. circ-ZEB1 downregulation suppressed NSCLC cell proliferation as well as migration in vitro and in vivo. Luciferase data confirmed EIF5A and miR-491-5p as downstream targets of circ-ZEB1. EIF5A overexpression and miR-491-5p suppression reversed NSCLC cell migration post circ-ZEB1 silencing. Our collective findings advised that circ-ZEB1 takes part in the malignant progression through regulating the miR-491-5p/EIF5A axis, highlighting its potential as an effective NSCLC therapeutic target.
环状RNA(circRNAs)是共价闭合的单链RNA,与癌症进展有关。先前的一项研究表明,circ-ZEB1在肝癌中异常表达。然而,circ-ZEB1在非小细胞肺癌(NSCLC)中的作用尚不清楚。在本研究中,我们使用荧光原位杂交(FISH)和RT-qPCR来研究circ-ZEB1在NSCLC细胞和组织中的表达。进行荧光素酶报告基因测定以验证circ-ZEB1的下游靶点。进行Transwell迁移、5-乙炔基-2'-脱氧尿苷(EdU)和细胞计数试剂盒8(CCK8)测定以评估增殖和迁移。还进行了体内转移和肿瘤发生测定以研究circ-ZEB1在NSCLC中的功能。我们的结果表明,circ-ZEB1在NSCLC组织和细胞中的表达增加。circ-ZEB1的下调抑制了NSCLC细胞在体外和体内的增殖以及迁移。荧光素酶数据证实EIF5A和miR-491-5p是circ-ZEB1的下游靶点。EIF5A的过表达和miR-491-5p的抑制逆转了circ-ZEB1沉默后NSCLC细胞的迁移。我们的研究结果表明,circ-ZEB1通过调节miR-491-5p/EIF5A轴参与恶性进展,突出了其作为有效的NSCLC治疗靶点的潜力。