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首页> 外文期刊>Cellular Physiology and Biochemistry >Analysis of lncRNA-Associated ceRNA Network Reveals Potential lncRNA Biomarkers in Human Colon Adenocarcinoma
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Analysis of lncRNA-Associated ceRNA Network Reveals Potential lncRNA Biomarkers in Human Colon Adenocarcinoma

机译:与lncRNA相关的ceRNA网络的分析揭示了人类结肠腺癌中潜在的lncRNA生物标志物。

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Background/Aims Long non-coding RNAs (lncRNAs) acting as competing endogenous RNAs (ceRNAs) play significant roles in the development of tumors, but the functions of specific lncRNAs and lncRNA-related ceRNA networks have not been fully elucidated for colon adenocarcinoma (COAD). In this study, we aimed to clarify the lncRNA-microRNA (miRNA)-mRNA ceRNA network and potential lncRNA biomarkers in COAD. Methods We extracted data from The Cancer Genome Atlas (TCGA) and identified COAD-specific mRNAs, miRNAs, and lncRNAs. The biological processes in Gene Ontology (GO) and the Kyoto Encyclopedia of Genes and Genomes (KEGG) were analyzed for COAD-specific mRNAs. We then constructed a ceRNA network of COAD-specific mRNAs, miRNAs and lncRNAs and analyzed the correlation between expression patterns and clinical features of the lncRNAs involved. After identifying potential mRNA targets of 4 lncRNAs related to overall survival (OS), we conducted stepwise analysis of these targets through GO and KEGG. Using tissue samples from our own patients, we also verified certain analytical results using quantitative real-time PCR (qRT-PCR). Results Data from 521 samples (480 tumor tissue and 41 adjacent non-tumor tissue samples) were extracted from TCGA. A total of 258 specific lncRNAs, 206 specific miRNAs, and 1467 specific mRNAs were identified (absolute log2 [fold change] > 2, false discovery rate < 0.01). Analysis of KEGG revealed that specific mRNAs were enriched in cancer-related pathways. The ceRNA network was constructed with 64 lncRNAs, 18 miRNAs, and 42 mRNAs. Among these lncRNAs involved in the network, 3 lncRNAs (LINC00355, HULC, and IGF2-AS) were confirmed to be associated with certain clinical features and 4 lncRNAs (HOTAIR, LINC00355, KCNQ1OT1, and TSSC1-IT1) were found to be negatively linked to OS (log-rank p < 0.05). KEGG showed that the potential mRNA targets of these 4 lncRNAs may be concentrated in the MAPK pathway. Certain results were validated by qRT-PCR. Conclusion This study providing novel insights into the lncRNA-miRNA-mRNA ceRNA network and reveals potential lncRNA biomarkers in COAD.
机译:背景/目的长的非编码RNA(lncRNA)充当竞争性内源RNA(ceRNA)在肿瘤的发展中起着重要作用,但尚未完全阐明特定lncRNAs和与lncRNA相关的ceRNA网络的功能以用于结肠腺癌(COAD)。 )。在这项研究中,我们旨在阐明COAD中的lncRNA-microRNA(miRNA)-mRNA ceRNA网络和潜在的lncRNA生物标记。方法我们从癌症基因组图谱(TCGA)中提取数据,并鉴定了COAD特异性mRNA,miRNA和lncRNA。分析了基因本体论(GO)和《京都基因与基因组百科全书》(KEGG)中的生物过程中COAD特异性mRNA的表达。然后,我们构建了一个由COAD特异性mRNA,miRNA和lncRNA组成的ceRNA网络,并分析了表达模式与所涉及的lncRNA的临床特征之间的相关性。在确定了4个与总生存期(OS)相关的lncRNA的潜在mRNA靶标后,我们通过GO和KEGG逐步分析了这些靶标。使用我们自己患者的组织样本,我们还使用定量实时PCR(qRT-PCR)验证了某些分析结果。结果从TCGA中提取了521个样本(480个肿瘤组织和41个相邻的非肿瘤组织样本)中的数据。总共鉴定了258个特异性lncRNA,206个特异性miRNA和1467个特异性mRNA(绝对log2 [倍数变化]& 2,错误发现率< 0.01)。 KEGG的分析表明,特定的mRNA在癌症相关途径中富集。 ceRNA网络由64个lncRNA,18个miRNA和42个mRNA组成。在网络中涉及的这些lncRNA中,证实有3个lncRNA(LINC00355,HULC和IGF2-AS)与某些临床特征相关,并且发现4个lncRNA(HOTAIR,LINC00355,KCNQ1OT1和TSSC1-IT1)具有负相关。操作系统(log-rank p< 0.05)。 KEGG表明,这4种lncRNA的潜在mRNA靶标可能集中在MAPK途径中。通过qRT-PCR验证了某些结果。结论这项研究为lncRNA-miRNA-mRNA ceRNA网络提供了新颖的见解,并揭示了COAD中潜在的lncRNA生物标志物。

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