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Predicting drug-induced transcriptome responses of a wide range of human cell lines by a novel tensor-train decomposition algorithm

MOTIVATION: Genome-wide identification of the transcriptomic responses of human cell lines to drug treatments is a challenging issue in medical and pharmaceutical research. However, drug-induced gene expression profiles are largely unknown and unobserved for all combinations of drugs and human cell...

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Autores principales: Iwata, Michio, Yuan, Longhao, Zhao, Qibin, Tabei, Yasuo, Berenger, Francois, Sawada, Ryusuke, Akiyoshi, Sayaka, Hamano, Momoko, Yamanishi, Yoshihiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6612872/
https://www.ncbi.nlm.nih.gov/pubmed/31510663
http://dx.doi.org/10.1093/bioinformatics/btz313
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author Iwata, Michio
Yuan, Longhao
Zhao, Qibin
Tabei, Yasuo
Berenger, Francois
Sawada, Ryusuke
Akiyoshi, Sayaka
Hamano, Momoko
Yamanishi, Yoshihiro
author_facet Iwata, Michio
Yuan, Longhao
Zhao, Qibin
Tabei, Yasuo
Berenger, Francois
Sawada, Ryusuke
Akiyoshi, Sayaka
Hamano, Momoko
Yamanishi, Yoshihiro
author_sort Iwata, Michio
collection PubMed
description MOTIVATION: Genome-wide identification of the transcriptomic responses of human cell lines to drug treatments is a challenging issue in medical and pharmaceutical research. However, drug-induced gene expression profiles are largely unknown and unobserved for all combinations of drugs and human cell lines, which is a serious obstacle in practical applications. RESULTS: Here, we developed a novel computational method to predict unknown parts of drug-induced gene expression profiles for various human cell lines and predict new drug therapeutic indications for a wide range of diseases. We proposed a tensor-train weighted optimization (TT-WOPT) algorithm to predict the potential values for unknown parts in tensor-structured gene expression data. Our results revealed that the proposed TT-WOPT algorithm can accurately reconstruct drug-induced gene expression data for a range of human cell lines in the Library of Integrated Network-based Cellular Signatures. The results also revealed that in comparison with the use of original gene expression profiles, the use of imputed gene expression profiles improved the accuracy of drug repositioning. We also performed a comprehensive prediction of drug indications for diseases with gene expression profiles, which suggested many potential drug indications that were not predicted by previous approaches. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
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spelling pubmed-66128722019-07-12 Predicting drug-induced transcriptome responses of a wide range of human cell lines by a novel tensor-train decomposition algorithm Iwata, Michio Yuan, Longhao Zhao, Qibin Tabei, Yasuo Berenger, Francois Sawada, Ryusuke Akiyoshi, Sayaka Hamano, Momoko Yamanishi, Yoshihiro Bioinformatics Ismb/Eccb 2019 Conference Proceedings MOTIVATION: Genome-wide identification of the transcriptomic responses of human cell lines to drug treatments is a challenging issue in medical and pharmaceutical research. However, drug-induced gene expression profiles are largely unknown and unobserved for all combinations of drugs and human cell lines, which is a serious obstacle in practical applications. RESULTS: Here, we developed a novel computational method to predict unknown parts of drug-induced gene expression profiles for various human cell lines and predict new drug therapeutic indications for a wide range of diseases. We proposed a tensor-train weighted optimization (TT-WOPT) algorithm to predict the potential values for unknown parts in tensor-structured gene expression data. Our results revealed that the proposed TT-WOPT algorithm can accurately reconstruct drug-induced gene expression data for a range of human cell lines in the Library of Integrated Network-based Cellular Signatures. The results also revealed that in comparison with the use of original gene expression profiles, the use of imputed gene expression profiles improved the accuracy of drug repositioning. We also performed a comprehensive prediction of drug indications for diseases with gene expression profiles, which suggested many potential drug indications that were not predicted by previous approaches. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online. Oxford University Press 2019-07 2019-07-05 /pmc/articles/PMC6612872/ /pubmed/31510663 http://dx.doi.org/10.1093/bioinformatics/btz313 Text en © The Author(s) 2019. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Ismb/Eccb 2019 Conference Proceedings
Iwata, Michio
Yuan, Longhao
Zhao, Qibin
Tabei, Yasuo
Berenger, Francois
Sawada, Ryusuke
Akiyoshi, Sayaka
Hamano, Momoko
Yamanishi, Yoshihiro
Predicting drug-induced transcriptome responses of a wide range of human cell lines by a novel tensor-train decomposition algorithm
title Predicting drug-induced transcriptome responses of a wide range of human cell lines by a novel tensor-train decomposition algorithm
title_full Predicting drug-induced transcriptome responses of a wide range of human cell lines by a novel tensor-train decomposition algorithm
title_fullStr Predicting drug-induced transcriptome responses of a wide range of human cell lines by a novel tensor-train decomposition algorithm
title_full_unstemmed Predicting drug-induced transcriptome responses of a wide range of human cell lines by a novel tensor-train decomposition algorithm
title_short Predicting drug-induced transcriptome responses of a wide range of human cell lines by a novel tensor-train decomposition algorithm
title_sort predicting drug-induced transcriptome responses of a wide range of human cell lines by a novel tensor-train decomposition algorithm
topic Ismb/Eccb 2019 Conference Proceedings
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6612872/
https://www.ncbi.nlm.nih.gov/pubmed/31510663
http://dx.doi.org/10.1093/bioinformatics/btz313
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