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Biologically informed deep neural network for prostate cancer discovery
The determination of molecular features that mediate clinically aggressive phenotypes in prostate cancer remains a major biological and clinical challenge(1,2). Recent advances in interpretability of machine learning models as applied to biomedical problems may enable discovery and prediction in cli...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8514339/ https://www.ncbi.nlm.nih.gov/pubmed/34552244 http://dx.doi.org/10.1038/s41586-021-03922-4 |
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author | Elmarakeby, Haitham A. Hwang, Justin Arafeh, Rand Crowdis, Jett Gang, Sydney Liu, David AlDubayan, Saud H. Salari, Keyan Kregel, Steven Richter, Camden Arnoff, Taylor E. Park, Jihye Hahn, William C. Van Allen, Eliezer M. |
author_facet | Elmarakeby, Haitham A. Hwang, Justin Arafeh, Rand Crowdis, Jett Gang, Sydney Liu, David AlDubayan, Saud H. Salari, Keyan Kregel, Steven Richter, Camden Arnoff, Taylor E. Park, Jihye Hahn, William C. Van Allen, Eliezer M. |
author_sort | Elmarakeby, Haitham A. |
collection | PubMed |
description | The determination of molecular features that mediate clinically aggressive phenotypes in prostate cancer remains a major biological and clinical challenge(1,2). Recent advances in interpretability of machine learning models as applied to biomedical problems may enable discovery and prediction in clinical cancer genomics(3–5). Here we developed P-NET—a biologically informed deep learning model—to stratify patients with prostate cancer by treatment-resistance state and evaluate molecular drivers of treatment resistance for therapeutic targeting through complete model interpretability. We demonstrate that P-NET can predict cancer state using molecular data with a performance that is superior to other modelling approaches. Moreover, the biological interpretability within P-NET revealed established and novel molecularly altered candidates, such as MDM4 and FGFR1, which were implicated in predicting advanced disease and validated in vitro. Broadly, biologically informed fully interpretable neural networks enable preclinical discovery and clinical prediction in prostate cancer and may have general applicability across cancer types. |
format | Online Article Text |
id | pubmed-8514339 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-85143392021-10-29 Biologically informed deep neural network for prostate cancer discovery Elmarakeby, Haitham A. Hwang, Justin Arafeh, Rand Crowdis, Jett Gang, Sydney Liu, David AlDubayan, Saud H. Salari, Keyan Kregel, Steven Richter, Camden Arnoff, Taylor E. Park, Jihye Hahn, William C. Van Allen, Eliezer M. Nature Article The determination of molecular features that mediate clinically aggressive phenotypes in prostate cancer remains a major biological and clinical challenge(1,2). Recent advances in interpretability of machine learning models as applied to biomedical problems may enable discovery and prediction in clinical cancer genomics(3–5). Here we developed P-NET—a biologically informed deep learning model—to stratify patients with prostate cancer by treatment-resistance state and evaluate molecular drivers of treatment resistance for therapeutic targeting through complete model interpretability. We demonstrate that P-NET can predict cancer state using molecular data with a performance that is superior to other modelling approaches. Moreover, the biological interpretability within P-NET revealed established and novel molecularly altered candidates, such as MDM4 and FGFR1, which were implicated in predicting advanced disease and validated in vitro. Broadly, biologically informed fully interpretable neural networks enable preclinical discovery and clinical prediction in prostate cancer and may have general applicability across cancer types. Nature Publishing Group UK 2021-09-22 2021 /pmc/articles/PMC8514339/ /pubmed/34552244 http://dx.doi.org/10.1038/s41586-021-03922-4 Text en © The Author(s), under exclusive licence to Springer Nature Limited 2021 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 Elmarakeby, Haitham A. Hwang, Justin Arafeh, Rand Crowdis, Jett Gang, Sydney Liu, David AlDubayan, Saud H. Salari, Keyan Kregel, Steven Richter, Camden Arnoff, Taylor E. Park, Jihye Hahn, William C. Van Allen, Eliezer M. Biologically informed deep neural network for prostate cancer discovery |
title | Biologically informed deep neural network for prostate cancer discovery |
title_full | Biologically informed deep neural network for prostate cancer discovery |
title_fullStr | Biologically informed deep neural network for prostate cancer discovery |
title_full_unstemmed | Biologically informed deep neural network for prostate cancer discovery |
title_short | Biologically informed deep neural network for prostate cancer discovery |
title_sort | biologically informed deep neural network for prostate cancer discovery |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8514339/ https://www.ncbi.nlm.nih.gov/pubmed/34552244 http://dx.doi.org/10.1038/s41586-021-03922-4 |
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