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Transcriptome sequencing uncovers a three–long noncoding RNA signature in predicting breast cancer survival

机译:转录组测序在预测乳腺癌生存揭露三长链非编码RNA签名

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Long noncoding RNAs (lncRNAs) play a crucial role in tumorigenesis. The aim of this study is to identify lncRNA signature that can predict breast cancer patient survival. RNA expression data from 1064 patients were downloaded from The Cancer Genome Atlas project. Cox regression, Kaplan-Meier, and receiver operating characteristic (ROC) analyses were performed to construct a model for predicting the overall survival (OS) of patients and evaluate it. A model consisting of three lncRNA genes (CAT104, LINC01234, and STXBP5-AS1) was identified. The Kaplan-Meier analysis and ROC curves proved that the model could predict the prognostic survival with good sensitivity and specificity in both the validation set (AUC?=?0.752, 95% confidence intervals (CI): 0.651-0.854) and the microarray dataset (AUC?=?0.714, 95%CI: 0.615-0.814). Further study showed the three-lncRNA signature was not only pervasive in different breast cancer stages, subtypes and age groups, but also provides more accurate prognostic information than some widely known biomarkers. The results suggested that RNA-seq transcriptome profiling provides that the three-lncRNA signature is an independent prognostic biomarker, and have clinical significance. In addition, lncRNA, miRNA, and mRNA interaction network indicated lncRNAs may intervene in breast cancer pathogenesis by binding to miR-190b, acting as competing endogenous RNAs.
机译:长度非编码RNA(LNCRNA)在肿瘤发生中发挥至关重要的作用。本研究的目的是鉴定可以预测乳腺癌患者存活的LNCRNA签名。来自1064名患者的RNA表达数据从癌症基因组Atlas项目下载。进行Cox回归,Kaplan-Meier和接收器操作特征(ROC)分析,以构建预测患者整体存活(OS)的模型并评估它。鉴定了由三种LNCRNA基因组成的模型(CAT104,LINC01234和STXBP5-AS1)。 Kaplan-Meier分析和ROC曲线证明了该模型可以预测验证集中具有良好敏感性和特异性的预后存活(AUC?= 0.752,95%置信区间(CI):0.651-0.854)和微阵列数据集(AUC?= 0.714,95%CI:0.615-0.814)。进一步的研究表明,三次患者签名不仅在不同的乳腺癌阶段,亚型和年龄组中普遍存在,而且还提供比某些众所周知的生物标志物更准确的预后信息。结果表明,RNA-SEQ转录组分析规定,三LNCRNA签名是一个独立的预后生物标志物,并具有临床意义。另外,LNCRNA,miRNA和mRNA相互作用网络所指出的LNCRNA可以通过与miR-190b结合,作为竞争内源RNA的乳腺癌发病机制。

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