MPVNN: Mutated Pathway Visible Neural Network architecture for interpretable prediction of cancer-specific survival risk

Author:

Ghosh Roy Gourab12ORCID,Geard Nicholas2,Verspoor Karin23ORCID,He Shan1ORCID

Affiliation:

1. School of Computer Science, University of Birmingham , Birmingham B15 2TT, UK

2. School of Computing and Information Systems, University of Melbourne , Melbourne 3052, Australia

3. School of Computing Technologies, RMIT University , Melbourne 3000, Australia

Abstract

Abstract Motivation Survival risk prediction using gene expression data is important in making treatment decisions in cancer. Standard neural network (NN) survival analysis models are black boxes with a lack of interpretability. More interpretable visible neural network architectures are designed using biological pathway knowledge. But they do not model how pathway structures can change for particular cancer types. Results We propose a novel Mutated Pathway Visible Neural Network (MPVNN) architecture, designed using prior signaling pathway knowledge and random replacement of known pathway edges using gene mutation data simulating signal flow disruption. As a case study, we use the PI3K-Akt pathway and demonstrate overall improved cancer-specific survival risk prediction of MPVNN over other similar-sized NN and standard survival analysis methods. We show that trained MPVNN architecture interpretation, which points to smaller sets of genes connected by signal flow within the PI3K-Akt pathway that is important in risk prediction for particular cancer types, is reliable. Availability and implementation The data and code are available at https://github.com/gourabghoshroy/MPVNN. Supplementary information Supplementary data are available at Bioinformatics online.

Funder

University of Birmingham

University of Melbourne

Publisher

Oxford University Press (OUP)

Subject

Computational Mathematics,Computational Theory and Mathematics,Computer Science Applications,Molecular Biology,Biochemistry,Statistics and Probability

Reference31 articles.

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