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

机译:基于基因对表达比的网络签名改善了肌肉浸润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:尿道癌(UC)高度复发,可以从非侵入性(NMIUC)演变成侵袭性更强的肌肉侵入(MIUC)亚型,侵入膀胱的肌肉组织层。我们提供了原理研究的证明,即基于基因对的网络特征可用于改善分类器性能和尿路上皮癌基因表达数据的功能分析。在我们程序的第一步中,UC基因表达数据集的每个样本都根据基于给定网络结构定义的基因对表达率进行了膨胀。在第二步中,使用基于网络的签名的弹性网络特征选择过程来区分NMIUC和MIUC样本。我们在三个独立的数据集中执行了重复的随机子采样交叉验证。网络签名通过功能富集分析进行表征,并研究已知癌症基因的富集。我们观察到蛋白质-蛋白质相互作用(PPI)数据库(如CPDB)和PPI数据库HPRD和BioGrid的元集合的基于网络的基因签名与基于单个基因的签名相比,改善了分类性能。源自PPI数据库的基于网络的签名显示出癌症基因(例如TP53,TRIM27和HNRNPA2B1)的显着丰富。我们为大规模基因表达分析提供了一种新颖的整合方法,用于鉴定和开发膀胱癌的新型诊断靶标。此外,我们的方法允许将癌症基因关联链接到在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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