Improving Cancer Survival Prediction via Graph Convolutional Neural Network Learning on Protein-Protein Interaction Networks

被引:3
作者
Cai, Hongmin [1 ]
Liao, Yi [1 ]
Zhu, Lei [1 ]
Wang, Zhikang [2 ,3 ]
Song, Jiangning [2 ,3 ]
机构
[1] South China Univ Technol, Sch Comp Sci & Engn, Guangzhou 510006, Peoples R China
[2] Monash Univ, Biomed Discovery Inst, Melbourne, Vic 3800, Australia
[3] Monash Univ, Dept Biochem & Mol Biol, Melbourne, Vic 3800, Australia
关键词
Survival analysis; protein-protein interaction; machine learning; graph convolutional network; BREAST-CANCER; CELL-ADHESION; PROGNOSIS; METASTASIS; GROWTH; MODELS; SYSTEM;
D O I
10.1109/JBHI.2023.3332640
中图分类号
TP [自动化技术、计算机技术];
学科分类号
0812 ;
摘要
Cancer is one of the most challenging health problems worldwide. Accurate cancer survival prediction is vital for clinical decision making. Many deep learning methods have been proposed to understand the association between patients' genomic features and survival time. In most cases, the gene expression matrix is fed directly to the deep learning model. However, this approach completely ignores the interactions between biomolecules, and the resulting models can only learn the expression levels of genes to predict patient survival. In essence, the interaction between biomolecules is the key to determining the direction and function of biological processes. Proteins are the building blocks and principal undertakings of life activities, and as such, their complex interaction network is potentially informative for deep learning methods. Therefore, a more reliable approach is to have the neural network learn both gene expression data and protein interaction networks. We propose a new computational approach, termed CRESCENT, which is a protein-protein interaction (PPI) prior knowledge graph-based convolutional neural network (GCN) to improve cancer survival prediction. CRESCENT relies on the gene expression networks rather than gene expression levels to predict patient survival. The performance of CRESCENT is evaluated on a large-scale pan-cancer dataset consisting of 5991 patients from 16 different types of cancers. Extensive benchmarking experiments demonstrate that our proposed method is competitive in terms of the evaluation metric of the time-dependent concordance index(${C}<^>{td}$) when compared with several existing state-of-the-art approaches. Experiments also show that incorporating the network structure between genomic features effectively improves cancer survival prediction.
引用
收藏
页码:1134 / 1143
页数:10
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