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Exploring prognostic potential of long noncoding RNAs in colorectal cancer based on a competing endogenous RNA network

机译:基于竞争内源性RNA网络探讨结直肠癌长型rNA的预后潜力

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BACKGROUND Colorectal cancer (CRC) is one of the most prevalent tumors worldwide. Recently, long noncoding RNAs (lncRNAs) have been shown to influence tumorigenesis and tumor progression by acting as competing endogenous RNAs (ceRNAs). It is difficult to extract prognostic lncRNAs and useful bioinformation from most ceRNA networks constructed previously. AIM To construct a prognostic related ceRNA regulatory network and lncRNA related signature based on risk score in CRC. METHODS RNA transcriptome profile and clinical information of 506 CRC patients were downloaded from the Cancer Genome Atlas database. R packages and Perl program were used for data processing. Cox regression analysis was used for prognostic model construction. Quantitative real-time polymerase chain reaction was used to detect the expression of lncRNAs. RESULTS A prognostic-related ceRNA network was constructed, including 9 lncRNAs, 44 mRNAs, and 30 miRNAs. In addition, a four-lncRNA model was constructed using multivariate Cox regression analysis, which could be an independent prognostic model in CRC. The risk score for each patient was calculated, and the 506 patients were divided into high and low-risk groups (253 for each group) based on the median risk score. The results of the survival analysis showed that patients with a high-risk score had a poor survival rate. Furthermore, the predictive value of the four-lncRNA model was evaluated in GSE38832. Patient survival probabilities could be better predicted when combing the risk score and clinical features. Gene Set Enrichment Analysis results verified that a number of cancer-related signaling pathways were enriched with a high-risk score in CRC. Finally, we validated a novel lncRNA ( LINC00488 ) using quantitative real-time polymerase chain reaction in 22 paired CRC patient tumor tissues compared to adjacent non-tumor tissues. CONCLUSION The four-lncRNA model could give better predictive value for CRC patients. Our understanding of the lncRNA-related ceRNA regulatory mechanism could provide a potential diagnostic indicator for CRC patients.
机译:背景背直肠癌(CRC)是全球最普遍的肿瘤之一。最近,已经证明了长的非分量RNA(LNCRNA)通过作为竞争内源性RNA(CERNAS)来影响肿瘤发生和肿瘤进展。难以从先前构建的大多数Cerna网络中提取预后的LNCRNA和有用的生物信息。旨在构建基于CRC风险评分的预后相关的Cerna调节网络和LNCRNA相关签名。方法从癌症基因组Atlas数据库下载506 rc患者的RNA转录组型和临床信息。 R包和Perl程序用于数据处理。 Cox回归分析用于预后模型建设。定量实时聚合酶链反应用于检测LNCRNA的表达。结果构建了预后相关的Cerna网络,包括9个LNCRNA,44 mRNA和30 miRNA。此外,使用多元COX回归分析构建了四LNCRNA模型,其可以是CRC中的独立预后模型。计算每位患者的风险评分,并根据中位风险评分,将506名患者分为高风险的群体(每组253例)。生存分析结果表明,高风险评分的患者的存活率差。此外,在GSE38832中评估了四LNCRNA模型的预测值。在梳理风险评分和临床特征时,可以更好地预测患者存活概率。基因设定富集分析结果证实,在CRC中富含了许多癌症相关的信号通路。最后,我们使用与相邻的非肿瘤组织相比,使用22个成对的CRC患者肿瘤组织中的定量实时聚合酶链反应进行了新的LNCRNA(LINC00488)。结论四LNCRNA模型可为CRC患者提供更好的预测值。我们对LNCRNA相关的Cerna调节机制的理解可以为CRC患者提供潜在的诊断指标。

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