ParsVNN: Parsimony visible neural networks for uncovering cancer-specific and drug-sensitive genes and pathways

Prediction of cancer-specific drug responses as well as identification of the corresponding drug-sensitive genes and pathways remains a major biological and clinical challenge. Deep learning models hold immense promise for better drug response predictions, but most of them cannot provide biological...

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Bibliographic Details
Main Authors: Huang, K. (Author), Huang, X. (Author), Johnson, T. (Author), Ma, J. (Author), Radovich, M. (Author), Wang, Y. (Author), Zhang, J. (Author)
Format: Article
Language:English
Published: Oxford University Press 2021
Subjects:
Online Access:View Fulltext in Publisher
LEADER 02825nam a2200397Ia 4500
001 10.1093-nargab-lqab097
008 220427s2021 CNT 000 0 und d
020 |a 26319268 (ISSN) 
245 1 0 |a ParsVNN: Parsimony visible neural networks for uncovering cancer-specific and drug-sensitive genes and pathways 
260 0 |b Oxford University Press  |c 2021 
856 |z View Fulltext in Publisher  |u https://doi.org/10.1093/nargab/lqab097 
520 3 |a Prediction of cancer-specific drug responses as well as identification of the corresponding drug-sensitive genes and pathways remains a major biological and clinical challenge. Deep learning models hold immense promise for better drug response predictions, but most of them cannot provide biological and clinical interpretability. Visible neural network (VNN) models have emerged to solve the problem by giving neurons biological meanings and directly casting biological networks into the models. However, the biological networks used in VNNs are often redundant and contain components that are irrelevant to the downstream predictions. Therefore, the VNNs using these redundant biological networks are overparameterized, which significantly limits VNNs' predictive and explanatory power. To overcome the problem, we treat the edges and nodes in biological networks used in VNNs as features and develop a sparse learning framework ParsVNN to learn parsimony VNNs with only edges and nodes that contribute the most to the prediction task. We applied ParsVNN to build cancer-specific VNN models to predict drug response for five different cancer types. We demonstrated that the parsimony VNNs built by ParsVNN are superior to other state-of-the-art methods in terms of prediction performance and identification of cancer driver genes. Furthermore, we found that the pathways selected by ParsVNN have great potential to predict clinical outcomes as well as recommend synergistic drug combinations. © 2021 The Author(s) 2021. Published by Oxford University Press on behalf of NAR Genomics and Bioinformatics. 
650 0 4 |a Article 
650 0 4 |a artificial neural network 
650 0 4 |a bioinformatics 
650 0 4 |a cancer diagnosis 
650 0 4 |a cancer patient 
650 0 4 |a cancer survival 
650 0 4 |a clinical outcome 
650 0 4 |a controlled study 
650 0 4 |a deep learning 
650 0 4 |a drug response 
650 0 4 |a human 
650 0 4 |a parsimony visible neural network 
650 0 4 |a prediction 
650 0 4 |a survival analysis 
650 0 4 |a synergistic effect 
650 0 4 |a tumor gene 
700 1 |a Huang, K.  |e author 
700 1 |a Huang, X.  |e author 
700 1 |a Johnson, T.  |e author 
700 1 |a Ma, J.  |e author 
700 1 |a Radovich, M.  |e author 
700 1 |a Wang, Y.  |e author 
700 1 |a Zhang, J.  |e author 
773 |t NAR Genomics and Bioinformatics