Institute of Tumor, School of Medicine, Taizhou University, Taizhou, China.
Department of Medical Laboratory, Taizhou Central Hospital, Taizhou University Hospital, Taizhou, China.
Pathol Oncol Res. 2021 Feb 3;27:587130. doi: 10.3389/pore.2021.587130. eCollection 2021.
Increasing evidence has displayed critical roles of circular RNAs (circRNAs) in tongue squamous cell carcinoma (TSCC). Hsa_circ_0043265 (circ_0043265) has been identified as a tumor suppressor in various tumors. Nevertheless, the critical roles of circ_0043265 in the initiation and progression of TSCC are yet to be fully elucidated. In our study, RNA and protein expressions were detected via qRT-PCR and Western blot. Cell proliferation, migration and invasion were evaluated via CCK-8 and transwell assays. The interactions between circ_0043265, miR-1243 and SALL1 were analyzed via bioinformatics analyses, RNA pull-down and luciferase assays, respectively. The current study demonstrated that circ_0043265 expression was downmodulated in TSCC tissues and cell lines (SCC25, SCC15, SCC9 and Cal27). Functionally, circ_0043265 overexpression led to an attenuation of cell proliferation, migration and invasion of SCC25 and Cal27 cells. Mechanistically, circ_0043265 acted as a competing endogenous RNA (ceRNA) via competitively sponging miR-1243, and restoration of miR-1243 rescued the inhibitory effects of circ_0043265 on cell proliferation, migration and invasion of SCC25 and Cal27 cells. Finally, it was observed that spalt like transcription factor 1 (SALL1), a potential target of miR-1243, was positively modulated via circ_0043265 in SCC25 and Cal27 cells, and SALL1 knockdown reversed the inhibitory effects of circ_0043265 on SCC25 and Cal27 cells. Collectively, the current study demonstrated that circ_0043265 was downmodulated in TSCC and was identified as a ceRNA that restrained the cell proliferation, migration and invasion of SCC25 and Cal27 cells via modulating the miR-1243/SALL1 axis.
越来越多的证据表明环状 RNA(circRNA)在舌鳞状细胞癌(TSCC)中发挥着关键作用。Hsa_circ_0043265(circ_0043265)已被确定为多种肿瘤中的肿瘤抑制因子。然而,circ_0043265 在 TSCC 的发生和发展中的关键作用仍有待充分阐明。在我们的研究中,通过 qRT-PCR 和 Western blot 检测 RNA 和蛋白质表达。通过 CCK-8 和 Transwell 测定评估细胞增殖、迁移和侵袭。通过生物信息学分析、RNA 下拉和荧光素酶测定分别分析 circ_0043265、miR-1243 和 SALL1 之间的相互作用。本研究表明,circ_0043265 在 TSCC 组织和细胞系(SCC25、SCC15、SCC9 和 Cal27)中表达下调。功能上,circ_0043265 的过表达导致 SCC25 和 Cal27 细胞的增殖、迁移和侵袭能力减弱。机制上,circ_0043265 通过竞争性结合 miR-1243 作为竞争性内源性 RNA(ceRNA),恢复 miR-1243 挽救了 circ_0043265 对 SCC25 和 Cal27 细胞增殖、迁移和侵袭的抑制作用。最后观察到,SALL1,miR-1243 的潜在靶标,通过 circ_0043265 在 SCC25 和 Cal27 细胞中被正调控,SALL1 敲低逆转了 circ_0043265 对 SCC25 和 Cal27 细胞的抑制作用。总之,本研究表明 circ_0043265 在 TSCC 中下调,并被鉴定为一种 ceRNA,通过调节 miR-1243/SALL1 轴来抑制 SCC25 和 Cal27 细胞的增殖、迁移和侵袭。