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Circ_0001178 regulates miR-382/VEGFA axis to facilitate hepatocellular carcinoma progression.
Cellular Signalling ( IF 4.4 ) Pub Date : 2020-03-30 , DOI: 10.1016/j.cellsig.2020.109621
Shan Gao 1 , Wei Hu 2 , Xin Huang 2 , Xingyue Huang 2 , Wenwei Chen 2 , Lidan Hao 2 , Zubing Chen 3 , Jian Wang 4 , Hailiang Wei 5
Affiliation  

Circular RNAs (circRNAs) have been reported to regulate the gene expression through sponging corresponding microRNAs in multiple malignant tumors, including hepatocellular carcinoma (HCC). Up to now, the effects of circ_0001178 in HCC are barely known. In our current work, we tested circ_0001178 expression in HCC tissues and HCC cells and found it was greatly elevated. Then, we evaluated the function of circ_0001178 on HCC cell proliferation. We found HepG2 and Huh-7 cell proliferation was repressed after circ_0001178 shRNA was infected into the cells. Moreover, flow cytometry evidenced that HepG2 and Huh-7 cell apoptosis was markedly triggered and cell cycle was arrested. Meanwhile, it was shown that HCC cell migration and invasion capacity were markedly inhibited by loss of circ_0001178. Knockdown of circ_0001178 restrained HCC tumor growth in vivo. Then, miR-382 was predicted and confirmed as the target of circ_0001178. Circ_0001178 was demonstrated to modulate miR-382 expression negatively. The effect of circ_0001178 on HCC tumor was rescued by miR-382 overexpression. Furthermore, vascular epithelial growth factor A (VEGFA) is identified in various cancers. Currently, VEGFA was proved to be the downstream target of miR-382. To conclude, this research revealed that circ_0001178 induced HCC progression via modulating miR-382 and VEGFA axis.

中文翻译:

Circ_0001178 调节 miR-382/VEGFA 轴以促进肝细胞癌进展。

据报道,环状 RNA (circRNAs) 通过在包括肝细胞癌 (HCC) 在内的多种恶性肿瘤中吸收相应的 microRNA 来调节基因表达。到目前为止,circ_0001178 在 HCC 中的作用还鲜为人知。在我们目前的工作中,我们测试了 circ_0001178 在 HCC 组织和 HCC 细胞中的表达,发现它大大升高。然后,我们评估了 circ_0001178 对 HCC 细胞增殖的作用。我们发现在 circ_0001178 shRNA 感染细胞后,HepG2 和 Huh-7 细胞增殖受到抑制。此外,流式细胞术证明 HepG2 和 Huh-7 细胞凋亡被显着触发,细胞周期被阻止。同时,表明 circ_0001178 的缺失显着抑制了 HCC 细胞的迁移和侵袭能力。circ_0001178 的敲低抑制了体内 HCC 肿瘤的生长。然后,miR-382被预测并确认为circ_0001178的靶标。Circ_0001178 被证明可以负向调节 miR-382 的表达。miR-382过表达挽救了circ_0001178对HCC肿瘤的影响。此外,血管上皮生长因子 A (VEGFA) 在各种癌症中得到鉴定。目前,VEGFA 被证明是 miR-382 的下游靶点。总之,这项研究表明,circ_0001178 通过调节 miR-382 和 VEGFA 轴诱导 HCC 进展。血管上皮生长因子 A (VEGFA) 在各种癌症中得到鉴定。目前,VEGFA 被证明是 miR-382 的下游靶点。总之,这项研究表明,circ_0001178 通过调节 miR-382 和 VEGFA 轴诱导 HCC 进展。血管上皮生长因子 A (VEGFA) 在各种癌症中得到鉴定。目前,VEGFA 被证明是 miR-382 的下游靶点。总之,这项研究表明,circ_0001178 通过调节 miR-382 和 VEGFA 轴诱导 HCC 进展。
更新日期:2020-03-30
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