He Jin-Hua, Li Yu-Guang, Han Ze-Ping, Zhou Jia-Bin, Chen Wei-Ming, Lv Yu-Bing, He Meng-Ling, Zuo Ji-Dong, Zheng Lei
Department of Laboratory Medicine, Central Hospital of Panyu District, Guangzhou, China.
Department of Laboratory Medicine, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Cell Physiol Biochem. 2018;49(4):1539-1550. doi: 10.1159/000493457. Epub 2018 Sep 13.
BACKGROUND/AIMS: Circular RNAs (circRNAs), a type of RNA that is widely expressed in human cells, have essential roles in the development and progression of cancer. CircRNAs contain microRNA (miRNA) binding sites and can function as miRNA sponges to regulate gene expression by removing the inhibitory effect of an miRNA on its target gene.
We used the bioinformatics software TargetScan and miRanda to predict circRNA-miRNA and miRNAi-Mrna interactions. Rate of inhibiting of proliferation was measured using a WST-8 cell proliferation assay. Clone formation ability was assessed with a clone formation inhibition test. Cell invasion and migration capacity was evaluated by performing a Transwell assay. Relative gene expression was assessed using quantitative real-time polymerase chain reaction and relative protein expression levels were determined with western blotting. circRNA and miRNA interaction was confirmed by dual-luciferase reporter and RNA-pull down assays.
In the present study, the miRNA hsa-miR-21-5p was a target of circRNA-ACAP2, and T lymphoma invasion and metastasis protein 1 (Tiam1) was identified as a target gene of hsa-miR-21-5p. CircRNA-ACAP2 and Tiam1 were shown to be highly expressed in colon cancer tissue and colon cancer SW480 cells, but miR-21-5p was expressed at a low level. SW480 cell proliferation was suppressed when the expression of circRNA-ACAP2 and Tiam1 was decreased and the expression of miR-21-5p was increased in vivo and in vitro. SW480 cell migration and invasion were also inhibited under the same circumstance. The circRNA-ACAP2 interaction regulated the expression of miR-21-5p, and miR-21-5p regulated the expression of Tiam1. Down-regulation of circRNA-ACAP2 promoted miR-21-5p expression, which further suppressed the transcription and translation of Tiam1.
The present study shows that the circRNA-ACAP2/hsa-miR-21-5p/Tiam1 regulatory feedback circuit could affect the proliferation, migration, and invasion of colon cancer SW480 cells. This was probably due to the fact that circRNA-ACAP2 could act as a miRNA sponge to regulate Tiam1 expression by removing the inhibitory effect of miR-21-5p on Tiam1 expression. The results from this study have revealed new insights into the pathogenicity of colon cancer and may provide novel therapeutic targets for the treatment of colon cancer.
背景/目的:环状RNA(circRNAs)是一类在人类细胞中广泛表达的RNA,在癌症的发生和发展中起着重要作用。环状RNA含有微小RNA(miRNA)结合位点,可作为miRNA海绵,通过消除miRNA对其靶基因的抑制作用来调节基因表达。
我们使用生物信息学软件TargetScan和miRanda来预测circRNA-miRNA和miRNA-mRNA相互作用。使用WST-8细胞增殖测定法测量增殖抑制率。通过克隆形成抑制试验评估克隆形成能力。通过Transwell试验评估细胞侵袭和迁移能力。使用定量实时聚合酶链反应评估相对基因表达,并通过蛋白质印迹法测定相对蛋白质表达水平。通过双荧光素酶报告基因和RNA下拉试验证实circRNA与miRNA的相互作用。
在本研究中,miRNA hsa-miR-21-5p是circRNA-ACAP2的靶标,并且T淋巴瘤侵袭和转移蛋白1(Tiam1)被鉴定为hsa-miR-21-5p的靶基因。circRNA-ACAP2和Tiam1在结肠癌组织和结肠癌SW480细胞中高表达,但miR-21-5p表达水平较低。在体内和体外,当circRNA-ACAP2和Tiam1的表达降低且miR-21-5p的表达增加时,SW480细胞增殖受到抑制。在相同情况下,SW480细胞的迁移和侵袭也受到抑制。circRNA-ACAP2相互作用调节miR-21-5p的表达,而miR-21-5p调节Tiam1的表达。circRNA-ACAP2的下调促进miR-21-5p的表达,这进一步抑制了Tiam1的转录和翻译。
本研究表明,circRNA-ACAP2/hsa-miR-21-5p/Tiam1调节反馈回路可能影响结肠癌SW480细胞的增殖、迁移和侵袭。这可能是由于circRNA-ACAP2可以作为miRNA海绵,通过消除miR-21-5p对Tiam1表达的抑制作用来调节Tiam1的表达。本研究结果为结肠癌的发病机制提供了新的见解,并可能为结肠癌的治疗提供新的治疗靶点。