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Inferring cancer common and specific gene networks via multi-layer joint graphical model
Cancer is a complex disease caused primarily by genetic variants. Reconstructing gene networks within tumors is essential for understanding the functional regulatory mechanisms of carcinogenesis. Advances in high-throughput sequencing technologies have provided tremendous opportunities for inferring...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Research Network of Computational and Structural Biotechnology
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9873583/ https://www.ncbi.nlm.nih.gov/pubmed/36733706 http://dx.doi.org/10.1016/j.csbj.2023.01.017 |
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author | Chen, Yuanxiao Zhang, Xiao-Fei Ou-Yang, Le |
author_facet | Chen, Yuanxiao Zhang, Xiao-Fei Ou-Yang, Le |
author_sort | Chen, Yuanxiao |
collection | PubMed |
description | Cancer is a complex disease caused primarily by genetic variants. Reconstructing gene networks within tumors is essential for understanding the functional regulatory mechanisms of carcinogenesis. Advances in high-throughput sequencing technologies have provided tremendous opportunities for inferring gene networks via computational approaches. However, due to the heterogeneity of the same cancer type and the similarities between different cancer types, it remains a challenge to systematically investigate the commonalities and specificities between gene networks of different cancer types, which is a crucial step towards precision cancer diagnosis and treatment. In this study, we propose a new sparse regularized multi-layer decomposition graphical model to jointly estimate the gene networks of multiple cancer types. Our model can handle various types of gene expression data and decomposes each cancer-type-specific network into three components, i.e., globally shared, partially shared and cancer-type-unique components. By identifying the globally and partially shared gene network components, our model can explore the heterogeneous similarities between different cancer types, and our identified cancer-type-unique components can help to reveal the regulatory mechanisms unique to each cancer type. Extensive experiments on synthetic data illustrate the effectiveness of our model in joint estimation of multiple gene networks. We also apply our model to two real data sets to infer the gene networks of multiple cancer subtypes or cell lines. By analyzing our estimated globally shared, partially shared, and cancer-type-unique components, we identified a number of important genes associated with common and specific regulatory mechanisms across different cancer types. |
format | Online Article Text |
id | pubmed-9873583 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Research Network of Computational and Structural Biotechnology |
record_format | MEDLINE/PubMed |
spelling | pubmed-98735832023-02-01 Inferring cancer common and specific gene networks via multi-layer joint graphical model Chen, Yuanxiao Zhang, Xiao-Fei Ou-Yang, Le Comput Struct Biotechnol J Research Article Cancer is a complex disease caused primarily by genetic variants. Reconstructing gene networks within tumors is essential for understanding the functional regulatory mechanisms of carcinogenesis. Advances in high-throughput sequencing technologies have provided tremendous opportunities for inferring gene networks via computational approaches. However, due to the heterogeneity of the same cancer type and the similarities between different cancer types, it remains a challenge to systematically investigate the commonalities and specificities between gene networks of different cancer types, which is a crucial step towards precision cancer diagnosis and treatment. In this study, we propose a new sparse regularized multi-layer decomposition graphical model to jointly estimate the gene networks of multiple cancer types. Our model can handle various types of gene expression data and decomposes each cancer-type-specific network into three components, i.e., globally shared, partially shared and cancer-type-unique components. By identifying the globally and partially shared gene network components, our model can explore the heterogeneous similarities between different cancer types, and our identified cancer-type-unique components can help to reveal the regulatory mechanisms unique to each cancer type. Extensive experiments on synthetic data illustrate the effectiveness of our model in joint estimation of multiple gene networks. We also apply our model to two real data sets to infer the gene networks of multiple cancer subtypes or cell lines. By analyzing our estimated globally shared, partially shared, and cancer-type-unique components, we identified a number of important genes associated with common and specific regulatory mechanisms across different cancer types. Research Network of Computational and Structural Biotechnology 2023-01-18 /pmc/articles/PMC9873583/ /pubmed/36733706 http://dx.doi.org/10.1016/j.csbj.2023.01.017 Text en © 2023 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Research Article Chen, Yuanxiao Zhang, Xiao-Fei Ou-Yang, Le Inferring cancer common and specific gene networks via multi-layer joint graphical model |
title | Inferring cancer common and specific gene networks via multi-layer joint graphical model |
title_full | Inferring cancer common and specific gene networks via multi-layer joint graphical model |
title_fullStr | Inferring cancer common and specific gene networks via multi-layer joint graphical model |
title_full_unstemmed | Inferring cancer common and specific gene networks via multi-layer joint graphical model |
title_short | Inferring cancer common and specific gene networks via multi-layer joint graphical model |
title_sort | inferring cancer common and specific gene networks via multi-layer joint graphical model |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9873583/ https://www.ncbi.nlm.nih.gov/pubmed/36733706 http://dx.doi.org/10.1016/j.csbj.2023.01.017 |
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