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Network signatures based on gene pair expression ratios improve classification and the analysis of muscle-invasive urothelial cancer

机译:基于基因对表达率的网络签名改善了肌肉侵袭性尿路上皮癌的分类和分析

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Urothelial cancer (UC) is highly recurrent and can progress from non-invasive (NMIUC) to a more aggressive muscle-invasive (MIUC) subtype that invades the muscle tissue layer of the bladder. We present a proof of principle study that network-based features of gene pairs can be used to improve classifier performance and the functional analysis of urothelial cancer gene expression data. In the first step of our procedure each individual sample of a UC gene expression dataset is inflated by gene pair expression ratios that are defined based on a given network structure. In the second step an elastic net feature selection procedure for network-based signatures is applied to discriminate between NMIUC and MIUC samples. We performed a repeated random subsampling cross validation in three independent datasets. The network signatures were characterized by a functional enrichment analysis and studied for the enrichment of known cancer genes. We observed that the network-based gene signatures from meta collections of protein-protein interaction (PPI) databases such as CPDB and the PPI databases HPRD and BioGrid improved the classification performance compared to single gene based signatures. The network based signatures that were derived from PPI databases showed a prominent enrichment of cancer genes (e.g., TP53, TRIM27 and HNRNPA2B1). We provide a novel integrative approach for large-scale gene expression analysis for the identification and development of novel diagnostical targets in bladder cancer. Further, our method allowed to link cancer gene associations to network-based expression signatures that are not observed in gene-based expression signatures.
机译:尿检癌(UC)具有高度复发性,可以从非侵入性(NMIUC)到更具侵略性的肌肉侵袭性(MIUC)亚型,该亚型患者侵入膀胱的肌肉组织层。我们提出了一个原理研究证明,基因对的基于网络的特征可以用于改善分类器性能和尿液癌基因表达数据的功能分析。在我们的步骤的第一步中,UC基因表达数据集的各种样品通过基于给定网络结构来定义的基因对表达比率膨胀。在第二步中,应用基于网络的签名的弹性网特征选择过程来区分NMIUC和MIUC样本。我们在三个独立数据集中执行了一个重复的随机限制交叉验证。网络签名的特征在于功能性富集分析,并研究了已知癌症基因的富集。我们观察到从蛋白质 - 蛋白质相互作用(PPI)数据库的荟萃收集基于网络的基因签名,例如CPDB和PPI数据库HPRD和BioGrid改善了与基因基因基因的签名相比的分类性能。衍生自PPI数据库的基于网络的签名显示癌基因的突出富集(例如,TP53,Trim27和HNRNPA2B1)。我们为大规模基因表达分析提供了一种新的综合性方法,用于膀胱癌新型诊断靶标的鉴定和发展。此外,我们的方法允许将癌症基因关联链接到基于基于基因的表达签名中未观察到的基于网络的表达签名。

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