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Patient-level proteomic network prediction by explainable artificial intelligence
Understanding the pathological properties of dysregulated protein networks in individual patients’ tumors is the basis for precision therapy. Functional experiments are commonly used, but cover only parts of the oncogenic signaling networks, whereas methods that reconstruct networks from omics data...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9174200/ https://www.ncbi.nlm.nih.gov/pubmed/35672443 http://dx.doi.org/10.1038/s41698-022-00278-4 |
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author | Keyl, Philipp Bockmayr, Michael Heim, Daniel Dernbach, Gabriel Montavon, Grégoire Müller, Klaus-Robert Klauschen, Frederick |
author_facet | Keyl, Philipp Bockmayr, Michael Heim, Daniel Dernbach, Gabriel Montavon, Grégoire Müller, Klaus-Robert Klauschen, Frederick |
author_sort | Keyl, Philipp |
collection | PubMed |
description | Understanding the pathological properties of dysregulated protein networks in individual patients’ tumors is the basis for precision therapy. Functional experiments are commonly used, but cover only parts of the oncogenic signaling networks, whereas methods that reconstruct networks from omics data usually only predict average network features across tumors. Here, we show that the explainable AI method layer-wise relevance propagation (LRP) can infer protein interaction networks for individual patients from proteomic profiling data. LRP reconstructs average and individual interaction networks with an AUC of 0.99 and 0.93, respectively, and outperforms state-of-the-art network prediction methods for individual tumors. Using data from The Cancer Proteome Atlas, we identify known and potentially novel oncogenic network features, among which some are cancer-type specific and show only minor variation among patients, while others are present across certain tumor types but differ among individual patients. Our approach may therefore support predictive diagnostics in precision oncology by inferring “patient-level” oncogenic mechanisms. |
format | Online Article Text |
id | pubmed-9174200 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-91742002022-06-09 Patient-level proteomic network prediction by explainable artificial intelligence Keyl, Philipp Bockmayr, Michael Heim, Daniel Dernbach, Gabriel Montavon, Grégoire Müller, Klaus-Robert Klauschen, Frederick NPJ Precis Oncol Article Understanding the pathological properties of dysregulated protein networks in individual patients’ tumors is the basis for precision therapy. Functional experiments are commonly used, but cover only parts of the oncogenic signaling networks, whereas methods that reconstruct networks from omics data usually only predict average network features across tumors. Here, we show that the explainable AI method layer-wise relevance propagation (LRP) can infer protein interaction networks for individual patients from proteomic profiling data. LRP reconstructs average and individual interaction networks with an AUC of 0.99 and 0.93, respectively, and outperforms state-of-the-art network prediction methods for individual tumors. Using data from The Cancer Proteome Atlas, we identify known and potentially novel oncogenic network features, among which some are cancer-type specific and show only minor variation among patients, while others are present across certain tumor types but differ among individual patients. Our approach may therefore support predictive diagnostics in precision oncology by inferring “patient-level” oncogenic mechanisms. Nature Publishing Group UK 2022-06-07 /pmc/articles/PMC9174200/ /pubmed/35672443 http://dx.doi.org/10.1038/s41698-022-00278-4 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Keyl, Philipp Bockmayr, Michael Heim, Daniel Dernbach, Gabriel Montavon, Grégoire Müller, Klaus-Robert Klauschen, Frederick Patient-level proteomic network prediction by explainable artificial intelligence |
title | Patient-level proteomic network prediction by explainable artificial intelligence |
title_full | Patient-level proteomic network prediction by explainable artificial intelligence |
title_fullStr | Patient-level proteomic network prediction by explainable artificial intelligence |
title_full_unstemmed | Patient-level proteomic network prediction by explainable artificial intelligence |
title_short | Patient-level proteomic network prediction by explainable artificial intelligence |
title_sort | patient-level proteomic network prediction by explainable artificial intelligence |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9174200/ https://www.ncbi.nlm.nih.gov/pubmed/35672443 http://dx.doi.org/10.1038/s41698-022-00278-4 |
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