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pdCSM-cancer: Using Graph-Based Signatures to Identify Small Molecules with Anticancer Properties
[Image: see text] The development of new, effective, and safe drugs to treat cancer remains a challenging and time-consuming task due to limited hit rates, restraining subsequent development efforts. Despite the impressive progress of quantitative structure–activity relationship and machine learning...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8317153/ https://www.ncbi.nlm.nih.gov/pubmed/34213323 http://dx.doi.org/10.1021/acs.jcim.1c00168 |
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author | Al-Jarf, Raghad de Sá, Alex G. C. Pires, Douglas E. V. Ascher, David B. |
author_facet | Al-Jarf, Raghad de Sá, Alex G. C. Pires, Douglas E. V. Ascher, David B. |
author_sort | Al-Jarf, Raghad |
collection | PubMed |
description | [Image: see text] The development of new, effective, and safe drugs to treat cancer remains a challenging and time-consuming task due to limited hit rates, restraining subsequent development efforts. Despite the impressive progress of quantitative structure–activity relationship and machine learning-based models that have been developed to predict molecule pharmacodynamics and bioactivity, they have had mixed success at identifying compounds with anticancer properties against multiple cell lines. Here, we have developed a novel predictive tool, pdCSM-cancer, which uses a graph-based signature representation of the chemical structure of a small molecule in order to accurately predict molecules likely to be active against one or multiple cancer cell lines. pdCSM-cancer represents the most comprehensive anticancer bioactivity prediction platform developed till date, comprising trained and validated models on experimental data of the growth inhibition concentration (GI50%) effects, including over 18,000 compounds, on 9 tumor types and 74 distinct cancer cell lines. Across 10-fold cross-validation, it achieved Pearson’s correlation coefficients of up to 0.74 and comparable performance of up to 0.67 across independent, non-redundant blind tests. Leveraging the insights from these cell line-specific models, we developed a generic predictive model to identify molecules active in at least 60 cell lines. Our final model achieved an area under the receiver operating characteristic curve (AUC) of up to 0.94 on 10-fold cross-validation and up to 0.94 on independent non-redundant blind tests, outperforming alternative approaches. We believe that our predictive tool will provide a valuable resource to optimizing and enriching screening libraries for the identification of effective and safe anticancer molecules. To provide a simple and integrated platform to rapidly screen for potential biologically active molecules with favorable anticancer properties, we made pdCSM-cancer freely available online at http://biosig.unimelb.edu.au/pdcsm_cancer. |
format | Online Article Text |
id | pubmed-8317153 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-83171532021-07-28 pdCSM-cancer: Using Graph-Based Signatures to Identify Small Molecules with Anticancer Properties Al-Jarf, Raghad de Sá, Alex G. C. Pires, Douglas E. V. Ascher, David B. J Chem Inf Model [Image: see text] The development of new, effective, and safe drugs to treat cancer remains a challenging and time-consuming task due to limited hit rates, restraining subsequent development efforts. Despite the impressive progress of quantitative structure–activity relationship and machine learning-based models that have been developed to predict molecule pharmacodynamics and bioactivity, they have had mixed success at identifying compounds with anticancer properties against multiple cell lines. Here, we have developed a novel predictive tool, pdCSM-cancer, which uses a graph-based signature representation of the chemical structure of a small molecule in order to accurately predict molecules likely to be active against one or multiple cancer cell lines. pdCSM-cancer represents the most comprehensive anticancer bioactivity prediction platform developed till date, comprising trained and validated models on experimental data of the growth inhibition concentration (GI50%) effects, including over 18,000 compounds, on 9 tumor types and 74 distinct cancer cell lines. Across 10-fold cross-validation, it achieved Pearson’s correlation coefficients of up to 0.74 and comparable performance of up to 0.67 across independent, non-redundant blind tests. Leveraging the insights from these cell line-specific models, we developed a generic predictive model to identify molecules active in at least 60 cell lines. Our final model achieved an area under the receiver operating characteristic curve (AUC) of up to 0.94 on 10-fold cross-validation and up to 0.94 on independent non-redundant blind tests, outperforming alternative approaches. We believe that our predictive tool will provide a valuable resource to optimizing and enriching screening libraries for the identification of effective and safe anticancer molecules. To provide a simple and integrated platform to rapidly screen for potential biologically active molecules with favorable anticancer properties, we made pdCSM-cancer freely available online at http://biosig.unimelb.edu.au/pdcsm_cancer. American Chemical Society 2021-07-02 2021-07-26 /pmc/articles/PMC8317153/ /pubmed/34213323 http://dx.doi.org/10.1021/acs.jcim.1c00168 Text en © 2021 The Authors. Published by American Chemical Society Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Al-Jarf, Raghad de Sá, Alex G. C. Pires, Douglas E. V. Ascher, David B. pdCSM-cancer: Using Graph-Based Signatures to Identify Small Molecules with Anticancer Properties |
title | pdCSM-cancer: Using Graph-Based Signatures to Identify
Small Molecules with Anticancer Properties |
title_full | pdCSM-cancer: Using Graph-Based Signatures to Identify
Small Molecules with Anticancer Properties |
title_fullStr | pdCSM-cancer: Using Graph-Based Signatures to Identify
Small Molecules with Anticancer Properties |
title_full_unstemmed | pdCSM-cancer: Using Graph-Based Signatures to Identify
Small Molecules with Anticancer Properties |
title_short | pdCSM-cancer: Using Graph-Based Signatures to Identify
Small Molecules with Anticancer Properties |
title_sort | pdcsm-cancer: using graph-based signatures to identify
small molecules with anticancer properties |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8317153/ https://www.ncbi.nlm.nih.gov/pubmed/34213323 http://dx.doi.org/10.1021/acs.jcim.1c00168 |
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