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Knowledge boosting: a graph-based integration approach with multi-omics data and genomic knowledge for cancer clinical outcome prediction

机译:知识增强:基于图的整合方法结合多组学数据和基因组知识可预测癌症临床结果

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>Objective Cancer can involve gene dysregulation via multiple mechanisms, so no single level of genomic data fully elucidates tumor behavior due to the presence of numerous genomic variations within or between levels in a biological system. We have previously proposed a graph-based integration approach that combines multi-omics data including copy number alteration, methylation, miRNA, and gene expression data for predicting clinical outcome in cancer. However, genomic features likely interact with other genomic features in complex signaling or regulatory networks, since cancer is caused by alterations in pathways or complete processes.>Methods Here we propose a new graph-based framework for integrating multi-omics data and genomic knowledge to improve power in predicting clinical outcomes and elucidate interplay between different levels. To highlight the validity of our proposed framework, we used an ovarian cancer dataset from The Cancer Genome Atlas for predicting stage, grade, and survival outcomes.>Results Integrating multi-omics data with genomic knowledge to construct pre-defined features resulted in higher performance in clinical outcome prediction and higher stability. For the grade outcome, the model with gene expression data produced an area under the receiver operating characteristic curve (AUC) of 0.7866. However, models of the integration with pathway, Gene Ontology, chromosomal gene set, and motif gene set consistently outperformed the model with genomic data only, attaining AUCs of 0.7873, 0.8433, 0.8254, and 0.8179, respectively.>Conclusions Integrating multi-omics data and genomic knowledge to improve understanding of molecular pathogenesis and underlying biology in cancer should improve diagnostic and prognostic indicators and the effectiveness of therapies.
机译:>目的癌症可能通过多种机制参与基因失调,因此,由于在生物系统中不同水平或不同水平之间存在大量基因组变异,因此没有单一水平的基因组数据能够充分阐明肿瘤的行为。我们先前已经提出了一种基于图的整合方法,该方法结合了包括拷贝数变化,甲基化,miRNA和基因表达数据在内的多组学数据,可预测癌症的临床结局。但是,由于癌症是由途径或完整过程的改变引起的,因此基因组特征可能会与复杂的信号传导或调控网络中的其他基因组特征发生相互作用。>方法在这里,我们提出了一个基于图的新框架来整合多组学数据和基因组知识可提高预测临床结果的能力,并阐明不同水平之间的相互作用。为了强调我们提出的框架的有效性,我们使用了来自The Cancer Genome Atlas的卵巢癌数据集来预测阶段,等级和生存结果。>结果将多组学数据与基因组学知识相结合,可以构建预定义的功能可提高临床结果预测的性能和稳定性。对于等级结果,带有基因表达数据的模型在接收器工作特征曲线(AUC)下产生了0.7866的面积。但是,仅通过基因组数据,与途径,基因本体论,染色体基因组和基序基因组整合的模型始终优于模型,获得的AUC分别为0.7873、0.8433、0.8254和0.8179。>结论 >整合多组学数据和基因组学知识,以增进对癌症分子发病机制和基础生物学的了解,应改善诊断和预后指标以及治疗的有效性。

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