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A Boolean-based machine learning framework identifies predictive biomarkers of HSP90-targeted therapy response in prostate cancer
Precision medicine has emerged as an important paradigm in oncology, driven by the significant heterogeneity of individual patients’ tumour. A key prerequisite for effective implementation of precision oncology is the development of companion biomarkers that can predict response to anti-cancer thera...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9892654/ https://www.ncbi.nlm.nih.gov/pubmed/36743211 http://dx.doi.org/10.3389/fmolb.2023.1094321 |
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author | Shin, Sung-Young Centenera, Margaret M. Hodgson, Joshua T. Nguyen, Elizabeth V. Butler, Lisa M. Daly, Roger J. Nguyen, Lan K. |
author_facet | Shin, Sung-Young Centenera, Margaret M. Hodgson, Joshua T. Nguyen, Elizabeth V. Butler, Lisa M. Daly, Roger J. Nguyen, Lan K. |
author_sort | Shin, Sung-Young |
collection | PubMed |
description | Precision medicine has emerged as an important paradigm in oncology, driven by the significant heterogeneity of individual patients’ tumour. A key prerequisite for effective implementation of precision oncology is the development of companion biomarkers that can predict response to anti-cancer therapies and guide patient selection for clinical trials and/or treatment. However, reliable predictive biomarkers are currently lacking for many anti-cancer therapies, hampering their clinical application. Here, we developed a novel machine learning-based framework to derive predictive multi-gene biomarker panels and associated expression signatures that accurately predict cancer drug sensitivity. We demonstrated the power of the approach by applying it to identify response biomarker panels for an Hsp90-based therapy in prostate cancer, using proteomic data profiled from prostate cancer patient-derived explants. Our approach employs a rational feature section strategy to maximise model performance, and innovatively utilizes Boolean algebra methods to derive specific expression signatures of the marker proteins. Given suitable data for model training, the approach is also applicable to other cancer drug agents in different tumour settings. |
format | Online Article Text |
id | pubmed-9892654 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-98926542023-02-03 A Boolean-based machine learning framework identifies predictive biomarkers of HSP90-targeted therapy response in prostate cancer Shin, Sung-Young Centenera, Margaret M. Hodgson, Joshua T. Nguyen, Elizabeth V. Butler, Lisa M. Daly, Roger J. Nguyen, Lan K. Front Mol Biosci Molecular Biosciences Precision medicine has emerged as an important paradigm in oncology, driven by the significant heterogeneity of individual patients’ tumour. A key prerequisite for effective implementation of precision oncology is the development of companion biomarkers that can predict response to anti-cancer therapies and guide patient selection for clinical trials and/or treatment. However, reliable predictive biomarkers are currently lacking for many anti-cancer therapies, hampering their clinical application. Here, we developed a novel machine learning-based framework to derive predictive multi-gene biomarker panels and associated expression signatures that accurately predict cancer drug sensitivity. We demonstrated the power of the approach by applying it to identify response biomarker panels for an Hsp90-based therapy in prostate cancer, using proteomic data profiled from prostate cancer patient-derived explants. Our approach employs a rational feature section strategy to maximise model performance, and innovatively utilizes Boolean algebra methods to derive specific expression signatures of the marker proteins. Given suitable data for model training, the approach is also applicable to other cancer drug agents in different tumour settings. Frontiers Media S.A. 2023-01-19 /pmc/articles/PMC9892654/ /pubmed/36743211 http://dx.doi.org/10.3389/fmolb.2023.1094321 Text en Copyright © 2023 Shin, Centenera, Hodgson, Nguyen, Butler, Daly and Nguyen. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Molecular Biosciences Shin, Sung-Young Centenera, Margaret M. Hodgson, Joshua T. Nguyen, Elizabeth V. Butler, Lisa M. Daly, Roger J. Nguyen, Lan K. A Boolean-based machine learning framework identifies predictive biomarkers of HSP90-targeted therapy response in prostate cancer |
title | A Boolean-based machine learning framework identifies predictive biomarkers of HSP90-targeted therapy response in prostate cancer |
title_full | A Boolean-based machine learning framework identifies predictive biomarkers of HSP90-targeted therapy response in prostate cancer |
title_fullStr | A Boolean-based machine learning framework identifies predictive biomarkers of HSP90-targeted therapy response in prostate cancer |
title_full_unstemmed | A Boolean-based machine learning framework identifies predictive biomarkers of HSP90-targeted therapy response in prostate cancer |
title_short | A Boolean-based machine learning framework identifies predictive biomarkers of HSP90-targeted therapy response in prostate cancer |
title_sort | boolean-based machine learning framework identifies predictive biomarkers of hsp90-targeted therapy response in prostate cancer |
topic | Molecular Biosciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9892654/ https://www.ncbi.nlm.nih.gov/pubmed/36743211 http://dx.doi.org/10.3389/fmolb.2023.1094321 |
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