Sun Chengming, Li Guodong, Liu Ming
Department of Hepatopancreatobiliary Surgery, Cancer Hospital Affiliated to Harbin Medical University, Harbin 150001, People's Republic of China.
Department of General Surgery, The Fourth Affiliated Hospital of Harbin Medical University, Harbin 150001, People's Republic of China.
Onco Targets Ther. 2020 Jun 29;13:6171-6180. doi: 10.2147/OTT.S256238. eCollection 2020.
Circular RNAs (circRNAs) play a key role in cancer development and progression. Previously, circ_0005394 was found to be highly expressed in hepatocellular carcinoma (HCC) screened by circRNA microarray. However, the research with regard to the functions and mechanisms of circ_0005394 in HCC remains unknown.
The expression of circ_0005394 in HCC was measured by qRT-PCR. The clinical relevance was evaluated by Fisher's exact test, Kaplan-Meier curves, and Cox regression model. Gain/loss-of function assays were performed to elucidate the functions of circ_0005394 in Huh-7 and HepG2 cells. Dual-luciferase reporter assay was applied to reveal the mechanism of circ_0005394.
circ_0005394 expression was higher in HCC tissues and cells than noncancerous samples and normal cell line, respectively. High expression of circ_0005394 was associated with larger tumor size, more advanced TNM stages, and poorer overall survival for the patients with HCC. Gain/loss-of function assays demonstrated its oncogenic role in cell growth, apoptosis, migration, and invasion. Mechanistically, miR-507 and miR-515-5p could be sponged by circ_0005394. Furthermore, E2F Transcription Factor 3 (E2F3) and C-X-C motif chemokine ligand 6 (CXCL6) were confirmed as the target of miR-507 and miR-515-5p, respectively. Rescue assay indicated that circ_0005394 facilitated HCC growth and invasion by regulating miR-507/E2F3 and miR-515-5p/CXCL6 signaling pathways.
This study uncovered an important role of circ_0005394 in regulating HCC progression, providing a novel perspective for clarifying its pathogenesis.
环状RNA(circRNAs)在癌症发生和发展中起关键作用。此前,通过环状RNA微阵列筛选发现circ_0005394在肝细胞癌(HCC)中高表达。然而,circ_0005394在HCC中的功能和机制研究仍不清楚。
采用qRT-PCR检测circ_0005394在HCC中的表达。通过Fisher精确检验、Kaplan-Meier曲线和Cox回归模型评估其临床相关性。进行功能获得/缺失实验以阐明circ_0005394在Huh-7和HepG2细胞中的功能。应用双荧光素酶报告基因实验揭示circ_0005394的作用机制。
circ_0005394在HCC组织和细胞中的表达分别高于癌旁样本和正常细胞系。circ_0005394的高表达与HCC患者更大的肿瘤大小、更晚的TNM分期及更差的总生存期相关。功能获得/缺失实验证明其在细胞生长、凋亡、迁移和侵袭中具有致癌作用。机制上,circ_0005394可作为miR-507和miR-515-5p的海绵。此外,分别证实E2F转录因子3(E2F3)和C-X-C基序趋化因子配体6(CXCL6)为miR-507和miR-515-5p的靶标。挽救实验表明circ_0005394通过调节miR-507/E2F3和miR-515-5p/CXCL6信号通路促进HCC生长和侵袭。
本研究揭示了circ_0005394在调节HCC进展中的重要作用,为阐明其发病机制提供了新的视角。