Yang Dejun, Hu Zunqi, Zhang Yu, Zhang Xin, Xu Jiapeng, Fu Hongbing, Zhu Zhenxin, Feng Dan, Cai Qingping
Department of Gastrointestinal Surgery, Changzheng Hospital, Navy Medical University, Shanghai, China.
Department of Oncology, Changhai Hospital, Navy Medical University, Shanghai, China.
Front Oncol. 2021 Feb 19;11:637761. doi: 10.3389/fonc.2021.637761. eCollection 2021.
Circular RNA is a kind of RNA with a covalently closed loop, which has a complex ability to modulate genes in the process of tumorigenesis and metastasis. Nevertheless, how circular RNA functions in gastric cancer (GC) remains unclear. The effect of circHIPK3 was studied here. Quantitative real-time PCR (qRT-PCR) was employed to found that circHIPK3 markedly increased in GC tissues and cell lines. And low expression of circHIPK3 suppressed the GC cells growing and metabolizing. Then the bioinformatics tool predicted the downstream target of circHIPK3, and it was proved by the dual-luciferase report experiment. According to the results of bioinformatics analysis and experimental data, it was clarified that circHIPK3 acted as a sponge of miR-637, releasing its direct target AKT1. The dual-luciferase assay revealed that mir-637 could bind circHIPK3 and AKT1. qRT-PCR data indicated that overexpression circHIPK3 led to the low level of miR-637 and overexpressed miR-637 would reduce AKT1 level. Finally, we demonstrated that the low expression of miR-637 or overexpression of AKT1 could attenuate the anti-proliferative effects of si-circHIPK3. These results suggest that the circHIPK3/miR-637/AKT1 regulatory pathway may be associated with the oncogene and growth of gastric cancer. In short, a new circular RNA circHIPK3 and its function are identified, and the regulatory pathway of circHIPK3/miR-637/AKT1 in the tumorigenesis and development of gastric cancer is discovered.
环状RNA是一种具有共价闭合环的RNA,在肿瘤发生和转移过程中具有复杂的基因调控能力。然而,环状RNA在胃癌(GC)中的作用机制仍不清楚。本文研究了circHIPK3的作用。采用定量实时PCR(qRT-PCR)发现circHIPK3在GC组织和细胞系中显著上调。circHIPK3低表达抑制GC细胞的生长和代谢。然后通过生物信息学工具预测circHIPK3的下游靶点,并通过双荧光素酶报告实验进行验证。根据生物信息学分析和实验数据结果,明确circHIPK3作为miR-637的海绵,释放其直接靶点AKT1。双荧光素酶实验表明mir-637可以结合circHIPK3和AKT1。qRT-PCR数据表明,过表达circHIPK3导致miR-637水平降低,而过表达miR-637会降低AKT1水平。最后,我们证明miR-637低表达或AKT1过表达可减弱si-circHIPK3的抗增殖作用。这些结果表明,circHIPK3/miR-637/AKT1调控通路可能与胃癌的致癌作用和生长相关。简而言之,鉴定了一种新的环状RNA circHIPK3及其功能,发现了circHIPK3/miR-637/AKT1在胃癌发生发展中的调控通路。