基于蛋白质网络的Lasso回归模型构建疾病- mirna功能相互作用。

Ala Qabaja, Mohammed Alshalalfa, Tarek A Bismar, Reda Alhajj
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引用次数: 24

摘要

背景:越来越多的证据表明microRNAs (miRNAs)与人类疾病有关。mirna是疾病范式中新的关键参与者,在几种人类疾病中发挥作用。mirna与疾病之间的功能关联在很大程度上仍不清楚,也远未完成。随着高通量功能基因组学技术的出现,可以推断疾病中失调的基因和生物学途径,现在可以通过整合不同的生物信息来推断疾病和生物分子之间的功能关联。结果:在这里,我们首先使用Lasso回归模型来识别与疾病特征相关的mirna作为概念证明。然后,我们提出了一种综合方法,利用来自微阵列实验和文本挖掘的疾病-基因关联,以及来自计算预测和蛋白质网络的mirna -基因关联来构建mirna与疾病之间的功能关联网络。使用ROC分析对金标准数据集验证了所提出模型的结果,结果令人鼓舞(AUC=0.81)。我们基于蛋白质网络的方法在前列腺癌和mirna之间发现了19个新的功能关联。使用miRNA表达数据和临床资料验证了新的19种关联,并显示出作为诊断和预后前列腺生物标志物的作用。提出的综合方法使我们能够重建mirna与人类疾病之间的功能关联,并揭示新发现的mirna的功能作用。结论:利用mirna的基因标记,Lasso回归发现疾病与mirna之间的关联。通过整合miRNA的下游效应来定义miRNA基因特征比单独使用miRNA特征表现出更好的性能。整合生物网络和多种数据来定义miRNA和疾病基因特征,在揭示miRNA与疾病之间的新功能关联方面表现出色。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Protein network-based Lasso regression model for the construction of disease-miRNA functional interactions.

Protein network-based Lasso regression model for the construction of disease-miRNA functional interactions.

Protein network-based Lasso regression model for the construction of disease-miRNA functional interactions.

Protein network-based Lasso regression model for the construction of disease-miRNA functional interactions.

Background: There is a growing body of evidence associating microRNAs (miRNAs) with human diseases. MiRNAs are new key players in the disease paradigm demonstrating roles in several human diseases. The functional association between miRNAs and diseases remains largely unclear and far from complete. With the advent of high-throughput functional genomics techniques that infer genes and biological pathways dysregulted in diseases, it is now possible to infer functional association between diseases and biological molecules by integrating disparate biological information.

Results: Here, we first used Lasso regression model to identify miRNAs associated with disease signature as a proof of concept. Then we proposed an integrated approach that uses disease-gene associations from microarray experiments and text mining, and miRNA-gene association from computational predictions and protein networks to build functional associations network between miRNAs and diseases. The findings of the proposed model were validated against gold standard datasets using ROC analysis and results were promising (AUC=0.81). Our protein network-based approach discovered 19 new functional associations between prostate cancer and miRNAs. The new 19 associations were validated using miRNA expression data and clinical profiles and showed to act as diagnostic and prognostic prostate biomarkers. The proposed integrated approach allowed us to reconstruct functional associations between miRNAs and human diseases and uncovered functional roles of newly discovered miRNAs.

Conclusions: Lasso regression was used to find associations between diseases and miRNAs using their gene signature. Defining miRNA gene signature by integrating the downstream effect of miRNAs demonstrated better performance than the miRNA signature alone. Integrating biological networks and multiple data to define miRNA and disease gene signature demonstrated high performance to uncover new functional associations between miRNAs and diseases.

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