环状泛素相关蛋白2通过激活Wnt/β-连环蛋白信号通路,吸附微小RNA-506-3p,促进骨肉瘤中SEMA6D表达,增强顺铂耐药性。

CircUBAP2 promotes SEMA6D expression to enhance the cisplatin resistance in osteosarcoma through sponging miR-506-3p by activating Wnt/β-catenin signaling pathway.

作者信息

Dong Lin, Qu Fangfei

机构信息

Department of Pharmacy, Yantai Affiliated Hospital of Binzhou Medical University, No. 717 Jinbu Avenue, Mouping District, Yantai, 264000, Shandong, China.

Department of Special Inspection, Yantai Affiliated Hospital of Binzhou Medical University, Yantai, Shandong, China.

出版信息

J Mol Histol. 2020 Aug;51(4):329-340. doi: 10.1007/s10735-020-09883-8. Epub 2020 May 29.

Abstract

The occurrence of chemo-resistance is an essential reason for the high morbidity of osteosarcoma (OS) patients. Circular RNAs (circRNAs) have been involved in the regulation of chemo-resistance in cancers. Semaphorins 6D (SEMA6D) is abnormally expressed in many cancers. However, the roles of circUBAP2 and SEMA6D in the chemo-resistance of OS are still unclear. Quantitative real-time polymerase chain reaction (qRT-PCR) was used to detect the expression levels of circUBAP2, SEMA6D and microRNA-506-3p (miR-506-3p). The cisplatin resistance and proliferation of cells were evaluated by 3-(4, 5-dimethyl-2 thiazolyl)-2, 5-diphenyl-2-H-tetrazolium bromide assay. Western blot analysis was performed to measure the protein levels of Wnt/β-catenin signaling pathway biomarkers and SEMA6D. Also, the apoptosis, migration and invasion of cells were assessed by Flow cytometry and Transwell assays, respectively. Besides, Dual-luciferase reporter assay was used to verify the interaction between miR-506-3p and circUBAP2 or SEMA6D. We found that the expression levels of circUBAP2 and SEMA6D were increased in cisplatin-resistant OS tissues and cells. Knockdown of circUBAP2 inhibited the cisplatin resistance, silenced Wnt/β-catenin signaling pathway, hindered cell proliferation, migration and invasion, and promoted apoptosis in cisplatin-resistant OS cells, all of which could be reversed by overexpression of SEMA6D. MiR-506-3p could be sponged by circUBAP2 and could target SEMA6D. The suppression of miR-506-3p overexpression on the progression of OS cisplatin resistance could be reversed by SEMA6D overexpression, while miR-506-3p inhibitor also could invert the inhibitory effect of circUBAP2 silencing on the progression of OS cisplatin resistance. In conclusion, CircUBAP2 and SEMA6D played active roles in the progression of OS cisplatin resistance through miR-506-3p, which might provide some new ideas for studying the countermeasures of OS resistance.

摘要

化疗耐药的发生是骨肉瘤(OS)患者高发病率的一个重要原因。环状RNA(circRNAs)参与了癌症化疗耐药的调控。信号素6D(SEMA6D)在许多癌症中异常表达。然而,circUBAP2和SEMA6D在OS化疗耐药中的作用仍不清楚。采用定量实时聚合酶链反应(qRT-PCR)检测circUBAP2、SEMA6D和微小RNA-506-3p(miR-506-3p)的表达水平。通过3-(4,5-二甲基-2-噻唑基)-2,5-二苯基-2-H-四唑溴盐法评估细胞的顺铂耐药性和增殖情况。进行蛋白质印迹分析以检测Wnt/β-连环蛋白信号通路生物标志物和SEMA6D的蛋白质水平。此外,分别通过流式细胞术和Transwell实验评估细胞的凋亡、迁移和侵袭情况。此外,采用双荧光素酶报告基因实验验证miR-506-3p与circUBAP2或SEMA6D之间的相互作用。我们发现,circUBAP2和SEMA6D在顺铂耐药的OS组织和细胞中表达水平升高。敲低circUBAP2可抑制顺铂耐药性,使Wnt/β-连环蛋白信号通路沉默,阻碍细胞增殖、迁移和侵袭,并促进顺铂耐药的OS细胞凋亡,而这些作用均可通过SEMA6D的过表达逆转。MiR-506-3p可被circUBAP2吸附,并可靶向SEMA6D。SEMA6D过表达可逆转miR-506-3p过表达对OS顺铂耐药进展的抑制作用,而miR-506-3p抑制剂也可逆转circUBAP2沉默对OS顺铂耐药进展的抑制作用。总之,CircUBAP2和SEMA6D通过miR-506-3p在OS顺铂耐药进展中发挥积极作用,这可能为研究OS耐药的对策提供一些新思路。

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