Knowledge-guided fuzzy logic modeling to infer cellular signaling networks from proteomic data
Modeling of signaling pathways is crucial for understanding and predicting cellular responses to drug treatments. However, canonical signaling pathways curated from literature are seldom context-specific and thus can hardly predict cell type-specific response to external perturbations; purely data-d...
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sg-ntu-dr.10356-1554012022-02-25T07:21:12Z Knowledge-guided fuzzy logic modeling to infer cellular signaling networks from proteomic data Liu, Hui Zhang, Fan Mishra, Shital Kumar Zhou, Shuigeng Zheng, Jie School of Computer Science and Engineering Biomedical Informatics Lab Engineering::Computer science and engineering Signaling Pathways Cellular Signaling Networks Hybrid Modeling Modeling of signaling pathways is crucial for understanding and predicting cellular responses to drug treatments. However, canonical signaling pathways curated from literature are seldom context-specific and thus can hardly predict cell type-specific response to external perturbations; purely data-driven methods also have drawbacks such as limited biological interpretability. Therefore, hybrid methods that can integrate prior knowledge and real data for network inference are highly desirable. In this paper, we propose a knowledge-guided fuzzy logic network model to infer signaling pathways by exploiting both prior knowledge and time-series data. In particular, the dynamic time warping algorithm is employed to measure the goodness of fit between experimental and predicted data, so that our method can model temporally-ordered experimental observations. We evaluated the proposed method on a synthetic dataset and two real phosphoproteomic datasets. The experimental results demonstrate that our model can uncover drug-induced alterations in signaling pathways in cancer cells. Compared with existing hybrid models, our method can model feedback loops so that the dynamical mechanisms of signaling networks can be uncovered from time-series data. By calibrating generic models of signaling pathways against real data, our method supports precise predictions of context-specific anticancer drug effects, which is an important step towards precision medicine. Ministry of Education (MOE) Published version This work was supported by MOE AcRF Tier 2 grant ARC 39/13 (MOE2013-T2-1-079), Ministry of Education, Singapore, and Shuigeng Zhou was supported by the National Natural Science Foundation of China under grants No. 61672113 and No. 61272380, China. 2022-02-25T07:21:12Z 2022-02-25T07:21:12Z 2016 Journal Article Liu, H., Zhang, F., Mishra, S. K., Zhou, S. & Zheng, J. (2016). Knowledge-guided fuzzy logic modeling to infer cellular signaling networks from proteomic data. Scientific Reports, 6(1), 35652-. https://dx.doi.org/10.1038/srep35652 2045-2322 https://hdl.handle.net/10356/155401 10.1038/srep35652 27774993 2-s2.0-84992573744 1 6 35652 en ARC 39/12 (MOE2013-T2-1-079) Scientific Reports 10.21979/N9/VLZWCL © 2016 The Author(s). This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. application/pdf |
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Engineering::Computer science and engineering Signaling Pathways Cellular Signaling Networks Hybrid Modeling Liu, Hui Zhang, Fan Mishra, Shital Kumar Zhou, Shuigeng Zheng, Jie Knowledge-guided fuzzy logic modeling to infer cellular signaling networks from proteomic data |
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Modeling of signaling pathways is crucial for understanding and predicting cellular responses to drug treatments. However, canonical signaling pathways curated from literature are seldom context-specific and thus can hardly predict cell type-specific response to external perturbations; purely data-driven methods also have drawbacks such as limited biological interpretability. Therefore, hybrid methods that can integrate prior knowledge and real data for network inference are highly desirable. In this paper, we propose a knowledge-guided fuzzy logic network model to infer signaling pathways by exploiting both prior knowledge and time-series data. In particular, the dynamic time warping algorithm is employed to measure the goodness of fit between experimental and predicted data, so that our method can model temporally-ordered experimental observations. We evaluated the proposed method on a synthetic dataset and two real phosphoproteomic datasets. The experimental results demonstrate that our model can uncover drug-induced alterations in signaling pathways in cancer cells. Compared with existing hybrid models, our method can model feedback loops so that the dynamical mechanisms of signaling networks can be uncovered from time-series data. By calibrating generic models of signaling pathways against real data, our method supports precise predictions of context-specific anticancer drug effects, which is an important step towards precision medicine. |
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School of Computer Science and Engineering |
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School of Computer Science and Engineering Liu, Hui Zhang, Fan Mishra, Shital Kumar Zhou, Shuigeng Zheng, Jie |
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Article |
author |
Liu, Hui Zhang, Fan Mishra, Shital Kumar Zhou, Shuigeng Zheng, Jie |
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Liu, Hui |
title |
Knowledge-guided fuzzy logic modeling to infer cellular signaling networks from proteomic data |
title_short |
Knowledge-guided fuzzy logic modeling to infer cellular signaling networks from proteomic data |
title_full |
Knowledge-guided fuzzy logic modeling to infer cellular signaling networks from proteomic data |
title_fullStr |
Knowledge-guided fuzzy logic modeling to infer cellular signaling networks from proteomic data |
title_full_unstemmed |
Knowledge-guided fuzzy logic modeling to infer cellular signaling networks from proteomic data |
title_sort |
knowledge-guided fuzzy logic modeling to infer cellular signaling networks from proteomic data |
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2022 |
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https://hdl.handle.net/10356/155401 |
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1725985767387299840 |