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Dr.VAE: improving drug response prediction via modeling of drug perturbation effects
MOTIVATION: Individualized drug response prediction is a fundamental part of personalized medicine for cancer. Great effort has been made to discover biomarkers or to develop machine learning methods for accurate drug response prediction in cancers. Incorporating prior knowledge of biological system...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6761940/ https://www.ncbi.nlm.nih.gov/pubmed/30850846 http://dx.doi.org/10.1093/bioinformatics/btz158 |
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author | Rampášek, Ladislav Hidru, Daniel Smirnov, Petr Haibe-Kains, Benjamin Goldenberg, Anna |
author_facet | Rampášek, Ladislav Hidru, Daniel Smirnov, Petr Haibe-Kains, Benjamin Goldenberg, Anna |
author_sort | Rampášek, Ladislav |
collection | PubMed |
description | MOTIVATION: Individualized drug response prediction is a fundamental part of personalized medicine for cancer. Great effort has been made to discover biomarkers or to develop machine learning methods for accurate drug response prediction in cancers. Incorporating prior knowledge of biological systems into these methods is a promising avenue to improve prediction performance. High-throughput cell line assays of drug-induced transcriptomic perturbation effects are a prior knowledge that has not been fully incorporated into a drug response prediction model yet. RESULTS: We introduce a unified probabilistic approach, Drug Response Variational Autoencoder (Dr.VAE), that simultaneously models both drug response in terms of viability and transcriptomic perturbations. Dr.VAE is a deep generative model based on variational autoencoders. Our experimental results showed Dr.VAE to do as well or outperform standard classification methods for 23 out of 26 tested Food and Drug Administration-approved drugs. In a series of ablation experiments we showed that the observed improvement of Dr.VAE can be credited to the incorporation of drug-induced perturbation effects with joint modeling of treatment sensitivity. AVAILABILITY AND IMPLEMENTATION: Processed data and software implementation using PyTorch (Paszke et al., 2017) are available at: https://github.com/rampasek/DrVAE. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online. |
format | Online Article Text |
id | pubmed-6761940 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-67619402019-10-02 Dr.VAE: improving drug response prediction via modeling of drug perturbation effects Rampášek, Ladislav Hidru, Daniel Smirnov, Petr Haibe-Kains, Benjamin Goldenberg, Anna Bioinformatics Original Papers MOTIVATION: Individualized drug response prediction is a fundamental part of personalized medicine for cancer. Great effort has been made to discover biomarkers or to develop machine learning methods for accurate drug response prediction in cancers. Incorporating prior knowledge of biological systems into these methods is a promising avenue to improve prediction performance. High-throughput cell line assays of drug-induced transcriptomic perturbation effects are a prior knowledge that has not been fully incorporated into a drug response prediction model yet. RESULTS: We introduce a unified probabilistic approach, Drug Response Variational Autoencoder (Dr.VAE), that simultaneously models both drug response in terms of viability and transcriptomic perturbations. Dr.VAE is a deep generative model based on variational autoencoders. Our experimental results showed Dr.VAE to do as well or outperform standard classification methods for 23 out of 26 tested Food and Drug Administration-approved drugs. In a series of ablation experiments we showed that the observed improvement of Dr.VAE can be credited to the incorporation of drug-induced perturbation effects with joint modeling of treatment sensitivity. AVAILABILITY AND IMPLEMENTATION: Processed data and software implementation using PyTorch (Paszke et al., 2017) are available at: https://github.com/rampasek/DrVAE. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online. Oxford University Press 2019-10-01 2019-03-08 /pmc/articles/PMC6761940/ /pubmed/30850846 http://dx.doi.org/10.1093/bioinformatics/btz158 Text en © The Author(s) 2019. Published by Oxford University Press. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Papers Rampášek, Ladislav Hidru, Daniel Smirnov, Petr Haibe-Kains, Benjamin Goldenberg, Anna Dr.VAE: improving drug response prediction via modeling of drug perturbation effects |
title | Dr.VAE: improving drug response prediction via modeling of drug perturbation effects |
title_full | Dr.VAE: improving drug response prediction via modeling of drug perturbation effects |
title_fullStr | Dr.VAE: improving drug response prediction via modeling of drug perturbation effects |
title_full_unstemmed | Dr.VAE: improving drug response prediction via modeling of drug perturbation effects |
title_short | Dr.VAE: improving drug response prediction via modeling of drug perturbation effects |
title_sort | dr.vae: improving drug response prediction via modeling of drug perturbation effects |
topic | Original Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6761940/ https://www.ncbi.nlm.nih.gov/pubmed/30850846 http://dx.doi.org/10.1093/bioinformatics/btz158 |
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