Issue 3, 2017

Topologically inferring pathway activity for precise survival outcome prediction: breast cancer as a case

Abstract

Accurately predicting the survival outcome of patients is of great importance in clinical cancer research. In the past decade, building survival prediction models based on gene expression data has received increasing interest. However, the existing methods are mainly based on individual gene signatures, which are known to have limited prediction accuracy on independent datasets and unclear biological relevance. Here, we propose a novel pathway-based survival prediction method called DRWPSurv in order to accurately predict survival outcome. DRWPSurv integrates gene expression profiles and prior gene interaction information to topologically infer survival associated pathway activities, and uses the pathway activities as features to construct Lasso-Cox model. It uses topological importance of genes evaluated by directed random walk to enhance the robustness of pathway activities and thereby improve the predictive performance. We applied DRWPSurv on three independent breast cancer datasets and compared the predictive performance with a traditional gene-based method and four pathway-based methods. Results showed that pathway-based methods obtained comparable or better predictive performance than the gene-based method, whereas DRWPSurv could predict survival outcome with better accuracy and robustness among the pathway-based methods. In addition, the risk pathways identified by DRWPSurv provide biologically informative models for breast cancer prognosis and treatment.

Graphical abstract: Topologically inferring pathway activity for precise survival outcome prediction: breast cancer as a case

Supplementary files

Article information

Article type
Paper
Submitted
07 Nov 2016
Accepted
06 Jan 2017
First published
09 Jan 2017

Mol. BioSyst., 2017,13, 537-548

Topologically inferring pathway activity for precise survival outcome prediction: breast cancer as a case

W. Liu, W. Wang, G. Tian, W. Xie, L. Lei, J. Liu, W. Huang, L. Xu and E. Li, Mol. BioSyst., 2017, 13, 537 DOI: 10.1039/C6MB00757K

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