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Circular RNA hsa_circ_0001649 inhibits hepatocellular carcinoma progression via multiple miRNAs sponge

机译:环状RNA hsa_circ_0001649通过多个miRNA海绵抑制肝癌的进展

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摘要

Circular RNA (circRNA) exerts an essential role in tumor development. Hsa_circ_0001649 (circ-0001649) was produced at the SHPRH gene locus containing exon 26-29. This study analyzed the specific mechanism of circ-0001649 in influencing the development of hepatocellular carcinoma (HCC). Relative levels of circ-0001649 in HCC cell lines and tissues were examined by qRT-PCR. The direct binding between circ-0001649 and miR-127-5p/miR-612/miR-4688 were verified through Dual-luciferase reporter gene assay, RNA Binding Protein Immunoprecipitation (RIP) assay and western blot detection. In vitro and in vivo regulatory roles of circ-0001649 in proliferative and migratory abilities of HCC were evaluated by EdU, Transwell and tumourigenicity assay, respectively. Results showed that circ-0001649 was markedly decreased in hepatocellular carcinoma cell lines and tumor tissues. Overexpression of circ-0001649 greatly inhibited proliferation and migration of HCC in vitro and in vivo. More importantly, we confirmed that circ-0001649 regulated cellular behaviors of HCC cells by targeting SHPRH. Furthermore, we determined that circ-0001649 served as a ceRNA to sponge miR-127-5p, miR-612 and miR-4688, thus activating SHPRH. In summary, our study showed that circ-0001649 was lowly expressed in HCC and inhibited HCC progression via multiple miRNAs sponge.
机译:环状RNA(circRNA)在肿瘤发展中起着至关重要的作用。 Hsa_circ_0001649(circ-0001649)在含有外显子26-29的SHPRH基因位点产生。本研究分析了circ-0001649影响肝细胞癌(HCC)发生的具体机制。通过qRT-PCR检测HCC细胞系和组织中circ-0001649的相对水平。通过双荧光素酶报告基因测定,RNA结合蛋白免疫沉淀(RIP)测定和蛋白质印迹检测,验证了circ-0001649与miR-127-5p / miR-612 / miR-4688之间的直接结合。分别通过EdU,Transwell和致瘤性分析评估了circ-0001649在HCC增殖和迁移能力中的体外和体内调节作用。结果表明,在肝细胞癌细胞系和肿瘤组织中,circ-0001649明显减少。 circ-0001649的过度表达在体外和体内都大大抑制了HCC的增殖和迁移。更重要的是,我们证实circ-0001649通过靶向SHPRH来调节HCC细胞的细胞行为。此外,我们确定circ-0001649可作为ceRNA海绵miR-127-5p,miR-612和miR-4688,从而激活SHPRH。总而言之,我们的研究表明circ-0001649在HCC中的表达较低,并通过多个miRNA海绵抑制了HCC的进程。

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