首页> 外文OA文献 >The CircRNA-ACAP2/Hsa-miR-21-5p/ Tiam1 Regulatory Feedback Circuit Affects the Proliferation, Migration, and Invasion of Colon Cancer SW480 Cells
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The CircRNA-ACAP2/Hsa-miR-21-5p/ Tiam1 Regulatory Feedback Circuit Affects the Proliferation, Migration, and Invasion of Colon Cancer SW480 Cells

机译:CircRNA-ACAP2 / HSA-MIR-21-5P / TIAM1调节反馈电路影响结肠癌SW480细胞的增殖,迁移和侵袭

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摘要

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. Methods: 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. Results: 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. Conclusion: 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.
机译:背景/目的:圆形的RNA(circRNAs),一个类型的RNA,其在人细胞中广泛表达,在癌的发展和进展重要作用。 CircRNAs含有微小RNA(miRNA)的结合位点并且可以用作miRNA的海绵通过在其靶基因去除miRNA的抑制效果,以调节基因表达。方法:采用生物信息学软件TargetScan和米兰达预测circRNA-miRNA和miRNAi体mRNA的相互作用。使用WST-8细胞增殖测定中测量抑制增殖的速率。克隆形成能力用克隆形成抑制试验评估。细胞侵袭和迁移的能力通过进行Transwell小室法进行评价。使用定量实时聚合酶链式反应和相对蛋白质表达水平与蛋白质印迹确定的相对的基因表达进行了评估。 circRNA和miRNA相互作用通过双荧光素酶报告和RNA的下拉实验证实。结果:在本研究中,miRNA的hsa-的miR-21-5p是circRNA-ACAP2的目标,和T淋巴瘤侵袭和转移蛋白1(Tiam1的)被鉴定为HSA-的miR-21-5p的靶基因。 CircRNA-ACAP2和Tiam1的显示出在结肠癌组织和结肠癌SW480细胞中高度表达,但的miR-21-5p在一个低的水平表达。当circRNA-ACAP2和中Tiam1的表达下降被抑制SW480细胞的增殖和miR-21-5p的表达在体内和体外增加。 SW480细胞迁移和侵入也分别在相同条件下抑制。所述circRNA-ACAP2相互作用调节的miR-21-5p的表达,和miR-21-5p调节中Tiam1的表达。下调circRNA-ACAP2的促进的miR-21-5p的表达,这进一步抑制中Tiam1的转录和翻译。结论:本研究表明,circRNA-ACAP2 / HSA-的miR-21-5p / Tiam1的调节反馈电路可能影响增殖,迁移,和结肠癌SW480细胞的侵袭。这可能是由于这样的事实,circRNA-ACAP2可以作为的miRNA海绵去除的miR-21-5p对中Tiam1表达的抑制作用调节Tiam1的表达作用。这项研究的结果揭示了新的见解肠癌的致病性和可用于结肠癌的治疗提供新的治疗靶点。

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