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环状RNA hsa_circ_0005909通过靶向miR-338-3p/HMGA1轴促进骨肉瘤细胞增殖。

CircRNA hsa_circ_0005909 Promotes Cell Proliferation of Osteosarcoma Cells by Targeting miR-338-3p/HMGA1 Axis.

作者信息

Zhang Cailong, Na Na, Liu Li, Qiu Yingzhu

机构信息

Department of Arthrology Surgery, The Affiliated Hospital of Qingdao University, Qingdao 266000, People's Republic of China.

Department of Obstetrics, Qingdao Eighth People's Hospital, Qingdao 266000, People's Republic of China.

出版信息

Cancer Manag Res. 2021 Jan 27;13:795-803. doi: 10.2147/CMAR.S285118. eCollection 2021.

DOI:10.2147/CMAR.S285118
PMID:33536787
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7850455/
Abstract

OBJECTIVE

Osteosarcoma (OS) is the most common malignant bone tumor in the pediatric population. The main goal of this study is to investigate the role of hsa_circ_0005909 and the underlying signaling pathway involved in OS.

METHODS

Cell proliferation was measured using a CCK-8 assay kit and clone formation assay. Change of RNA and protein expression was determined using RNA extract and quantitative real time PCR (RT-qPCR) assay and Western blotting, respectively. CircInteractome was used to predict the target of circRNA and starBase v2.0 was used to predict the target of miRNAs. Luciferase assay was used to confirm the predicted results from CircInteractome, starBase v2.0, and MirTarget2.

RESULTS

Expression of circ_0005909 was upregulated in both OS tissues and cell lines. The predicted results from CircInteractome, starBase v2.0, and MirTarget2 demonstrated that circ_0005909 could sponge miR-338-3p and that HGMA1 was the direct target of miR-338-3p. Cell viability and cell clones were inhibited by knockdown of circ_0005909 but increased by dual inhibition of circ_0005909 and miR-338-3p. Phosphorylation of ERK, Akt, and PI3K was inhibited by sh-circ_0005909, while this inhibition was repressed by co-transfection of sh-circ_0005909 and HGMA1.

CONCLUSION

Expression of circ_0005909 was upregulated in both OS tissues and cell lines which upregulated expression of HGMA1 through sponging miR-338-3p, resulting in the activation of MAPK-ERK and PI3K-Akt signaling pathways to promote the development of OS.

摘要

目的

骨肉瘤(OS)是儿童人群中最常见的恶性骨肿瘤。本研究的主要目的是探讨hsa_circ_0005909在骨肉瘤中的作用及其潜在的信号通路。

方法

使用CCK-8检测试剂盒和克隆形成试验检测细胞增殖。分别使用RNA提取和定量实时PCR(RT-qPCR)试验以及蛋白质免疫印迹法测定RNA和蛋白质表达的变化。使用CircInteractome预测circRNA的靶标,使用starBase v2.0预测miRNA的靶标。荧光素酶报告基因检测用于确认CircInteractome、starBase v2.0和MirTarget2的预测结果。

结果

circ_0005909在骨肉瘤组织和细胞系中均上调表达。CircInteractome、starBase v2.0和MirTarget2的预测结果表明,circ_0005909可以吸附miR-338-3p,而HGMA1是miR-338-3p的直接靶标。敲低circ_0005909可抑制细胞活力和细胞克隆,但同时抑制circ_0005909和miR-338-3p可使其增加。sh-circ_0005909可抑制ERK、Akt和PI3K的磷酸化,而共转染sh-circ_0005909和HGMA1可抑制这种抑制作用。

结论

circ_0005909在骨肉瘤组织和细胞系中均上调表达,其通过吸附miR-338-3p上调HGMA1的表达,从而激活MAPK-ERK和PI3K-Akt信号通路,促进骨肉瘤的发展。

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本文引用的文献

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