Identification of Conserved Pappalysin 1-Derived Circular RNA-Mediated Competing Endogenous RNA in Osteosarcoma.

IF 1.7 4区 生物学 Q4 EVOLUTIONARY BIOLOGY
Evolutionary Bioinformatics Pub Date : 2021-10-21 eCollection Date: 2021-01-01 DOI:10.1177/11769343211041379
Guang-Fu Ming, Bo-Hua Gao, Peng Chen
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引用次数: 0

Abstract

The etiology of osteosarcoma (OS) is complex and not fully understood till now. This study aimed to identify the miRNAs, circRNAs, and genes (mRNAs) that are differentially expressed in OS cell lines to investigate the mechanism of circRNA-associated competing endogenous RNAs (ceRNAs) in OS. Microarray datasets reporting mRNA (GSE70414), miRNA (GSE70367), and circRNA changes (GSE96964) in human OS cell lines were downloaded, differentially expressed (DE) RNAs were identified, and DEmRNAs were used for the annotation of Gene Ontology (GO) biological processes (BP), and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathways. The mechanisms of DEcircRNA-mediated ceRNAs were identified in a step-by-step process. A total of 326 DEmRNAs, 45 DEmiRNAs, and 110 DEcircRNAs were identified from 3 datasets. The DEmRNAs were associated with GO BP terms, including cholesterol biosynthetic process, angiogenesis, extracellular matrix organization and KEGG pathways, including p53 signaling pathway and biosynthesis of antibiotics. The final ceRNA network consisted of 8 DEcircRNAs, including 5 pappalysin (PAPPA) 1-derived DEcircRNAs (hsa_circ_0005456, hsa_circ_0088209, hsa_circ_0002052, hsa_circ_0088214 and has_circ_0008792, all downregulated), 3 DEmiRNAs (hsa-miR-760, hsa-miR-4665-5p and hsa-miR-4539, all upregulated), and downregulated genes (including MMP13 and HMOX1). The ceRNA regulation network of OS was built, which played important roles in the pathogenesis of OS and might be of great importance in therapy.

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Abstract Image

骨肉瘤中保守的Pappalysin - 1衍生环状RNA介导的竞争内源性RNA的鉴定。
骨肉瘤(OS)的病因复杂,目前尚未完全了解。本研究旨在鉴定OS细胞系中差异表达的miRNAs、circRNAs和基因(mrna),以探讨circrna相关的竞争内源性rna (ceRNAs)在OS中的作用机制。下载了人类OS细胞系中mRNA (GSE70414)、miRNA (GSE70367)和circRNA变化(GSE96964)的微阵列数据集,鉴定了差异表达(DE) rna,并将demrna用于基因本体(GO)生物过程(BP)和京都基因与基因组百科全书(KEGG)途径的注释。decircrna介导的cerna的机制是在一个循序渐进的过程中确定的。从3个数据集中共鉴定出326个demrna, 45个demirna和110个decircrna。DEmRNAs与GO BP相关,包括胆固醇生物合成过程、血管生成、细胞外基质组织和KEGG途径,包括p53信号通路和抗生素的生物合成。最终的ceRNA网络由8个DEcircRNAs组成,包括5个pappalysin (PAPPA) 1衍生的DEcircRNAs (hsa_circ_0005456、hsa_circ_0088209、hsa_circ_0002052、hsa_circ_0088214和has_circ_0008792,均下调)、3个DEmiRNAs (hsa-miR-760、hsa-miR-4665-5p和hsa-miR-4539,均上调)和下调基因(包括MMP13和HMOX1)。建立了OS的ceRNA调控网络,在OS的发病机制中发挥了重要作用,在治疗中可能具有重要意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Evolutionary Bioinformatics
Evolutionary Bioinformatics 生物-进化生物学
CiteScore
4.20
自引率
0.00%
发文量
25
审稿时长
12 months
期刊介绍: Evolutionary Bioinformatics is an open access, peer reviewed international journal focusing on evolutionary bioinformatics. The journal aims to support understanding of organismal form and function through use of molecular, genetic, genomic and proteomic data by giving due consideration to its evolutionary context.
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