System-Based Differential Gene Network Analysis for Characterizing a Sample-Specific Subnetwork

Gene network estimation is a method key to understanding a fundamental cellular system from high throughput omics data. However, the existing gene network analysis relies on having a sufficient number of samples and is required to handle a huge number of nodes and estimated edges, which remain diffi...

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Main Authors: Yoshihisa Tanaka, Yoshinori Tamada, Marie Ikeguchi, Fumiyoshi Yamashita, Yasushi Okuno
Format: Article
Language:English
Published: MDPI AG 2020-02-01
Series:Biomolecules
Subjects:
emt
Online Access:https://www.mdpi.com/2218-273X/10/2/306
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spelling doaj-fe60fe305d9f40498c717463ad55fe7a2020-11-25T02:20:56ZengMDPI AGBiomolecules2218-273X2020-02-0110230610.3390/biom10020306biom10020306System-Based Differential Gene Network Analysis for Characterizing a Sample-Specific SubnetworkYoshihisa Tanaka0Yoshinori Tamada1Marie Ikeguchi2Fumiyoshi Yamashita3Yasushi Okuno4Graduate School of Pharmaceutical Sciences, Kyoto University, Kyoto 606-8507, JapanGraduate School of Medicine, Kyoto University, Kyoto 606-8507, JapanGraduate School of Medicine, Kyoto University, Kyoto 606-8507, JapanGraduate School of Pharmaceutical Sciences, Kyoto University, Kyoto 606-8507, JapanRIKEN Cluster for Science, Technology and Innovation Hub, Medical Sciences Innovation Hub Program, Kanagawa 230-0045, JapanGene network estimation is a method key to understanding a fundamental cellular system from high throughput omics data. However, the existing gene network analysis relies on having a sufficient number of samples and is required to handle a huge number of nodes and estimated edges, which remain difficult to interpret, especially in discovering the clinically relevant portions of the network. Here, we propose a novel method to extract a biomedically significant subnetwork using a Bayesian network, a type of unsupervised machine learning method that can be used as an explainable and interpretable artificial intelligence algorithm. Our method quantifies sample specific networks using our proposed <i>Edge Contribution value</i> (ECv) based on the estimated system, which realizes condition-specific subnetwork extraction using a limited number of samples. We applied this method to the Epithelial-Mesenchymal Transition (EMT) data set that is related to the process of metastasis and thus prognosis in cancer biology. We established our method-driven EMT network representing putative gene interactions. Furthermore, we found that the sample-specific ECv patterns of this EMT network can characterize the survival of lung cancer patients. These results show that our method unveils the explainable network differences in biological and clinical features through artificial intelligence technology.https://www.mdpi.com/2218-273X/10/2/306gene networkdifferential network analysislung cancer survival analysisemt
collection DOAJ
language English
format Article
sources DOAJ
author Yoshihisa Tanaka
Yoshinori Tamada
Marie Ikeguchi
Fumiyoshi Yamashita
Yasushi Okuno
spellingShingle Yoshihisa Tanaka
Yoshinori Tamada
Marie Ikeguchi
Fumiyoshi Yamashita
Yasushi Okuno
System-Based Differential Gene Network Analysis for Characterizing a Sample-Specific Subnetwork
Biomolecules
gene network
differential network analysis
lung cancer survival analysis
emt
author_facet Yoshihisa Tanaka
Yoshinori Tamada
Marie Ikeguchi
Fumiyoshi Yamashita
Yasushi Okuno
author_sort Yoshihisa Tanaka
title System-Based Differential Gene Network Analysis for Characterizing a Sample-Specific Subnetwork
title_short System-Based Differential Gene Network Analysis for Characterizing a Sample-Specific Subnetwork
title_full System-Based Differential Gene Network Analysis for Characterizing a Sample-Specific Subnetwork
title_fullStr System-Based Differential Gene Network Analysis for Characterizing a Sample-Specific Subnetwork
title_full_unstemmed System-Based Differential Gene Network Analysis for Characterizing a Sample-Specific Subnetwork
title_sort system-based differential gene network analysis for characterizing a sample-specific subnetwork
publisher MDPI AG
series Biomolecules
issn 2218-273X
publishDate 2020-02-01
description Gene network estimation is a method key to understanding a fundamental cellular system from high throughput omics data. However, the existing gene network analysis relies on having a sufficient number of samples and is required to handle a huge number of nodes and estimated edges, which remain difficult to interpret, especially in discovering the clinically relevant portions of the network. Here, we propose a novel method to extract a biomedically significant subnetwork using a Bayesian network, a type of unsupervised machine learning method that can be used as an explainable and interpretable artificial intelligence algorithm. Our method quantifies sample specific networks using our proposed <i>Edge Contribution value</i> (ECv) based on the estimated system, which realizes condition-specific subnetwork extraction using a limited number of samples. We applied this method to the Epithelial-Mesenchymal Transition (EMT) data set that is related to the process of metastasis and thus prognosis in cancer biology. We established our method-driven EMT network representing putative gene interactions. Furthermore, we found that the sample-specific ECv patterns of this EMT network can characterize the survival of lung cancer patients. These results show that our method unveils the explainable network differences in biological and clinical features through artificial intelligence technology.
topic gene network
differential network analysis
lung cancer survival analysis
emt
url https://www.mdpi.com/2218-273X/10/2/306
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AT fumiyoshiyamashita systembaseddifferentialgenenetworkanalysisforcharacterizingasamplespecificsubnetwork
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