In silico HCT116 human colon cancer cell-based models en route to the discovery of lead-like anticancer drugs
Autor(a) principal: | |
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Data de Publicação: | 2018 |
Outros Autores: | , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
Texto Completo: | https://doi.org/10.3390/biom8030056 |
Resumo: | Financial support from Fundacao para a Ciencia e Tecnologia (FCT) Portugal, under Project PTDC/QUIQUI/119116/2010 and grants SFRH/BPD/108237/2015 (F.P.) and IF/00700/2014 (S.P.G.) are greatly appreciated. This work was also supported by the LAQV and UCIBIO, which are financed by national funds from FCT/MEC (UID/QUI/50006/2013 and UID/Multi/04378/2013), respectively) and co-financed by the ERDF under the PT2020 Partnership Agreement (POCI-01-0145-FEDER-007265 and POCI-010145-FEDER-007728, respectively), and by Programme grant SAICTPAC/0019/2015 funded by European Structural and Investment Funds through the COMPETE Programme and by National Funds through FCT. The NMR spectrometers are part of The National NMR Facility, supported by FCT (RECI/BBB-BQB/0230/2012). |
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In silico HCT116 human colon cancer cell-based models en route to the discovery of lead-like anticancer drugsAnticancer activityHCT116 cell lineMachine learning (ML)Marine natural products (MNPs)Marine-derived actinobacteriaMolecular descriptorsNMR descriptorsQuantitative structure-Activity relationship (QSAR)BiochemistryMolecular BiologySDG 3 - Good Health and Well-beingSDG 14 - Life Below WaterFinancial support from Fundacao para a Ciencia e Tecnologia (FCT) Portugal, under Project PTDC/QUIQUI/119116/2010 and grants SFRH/BPD/108237/2015 (F.P.) and IF/00700/2014 (S.P.G.) are greatly appreciated. This work was also supported by the LAQV and UCIBIO, which are financed by national funds from FCT/MEC (UID/QUI/50006/2013 and UID/Multi/04378/2013), respectively) and co-financed by the ERDF under the PT2020 Partnership Agreement (POCI-01-0145-FEDER-007265 and POCI-010145-FEDER-007728, respectively), and by Programme grant SAICTPAC/0019/2015 funded by European Structural and Investment Funds through the COMPETE Programme and by National Funds through FCT. The NMR spectrometers are part of The National NMR Facility, supported by FCT (RECI/BBB-BQB/0230/2012).To discover new inhibitors against the human colon carcinoma HCT116 cell line, two quantitative structure–activity relationship (QSAR) studies using molecular and nuclear magnetic resonance (NMR) descriptors were developed through exploration of machine learning techniques and using the value of half maximal inhibitory concentration (IC50). In the first approach, A, regression models were developed using a total of 7339 molecules that were extracted from the ChEMBL and ZINC databases and recent literature. The performance of the regression models was successfully evaluated by internal and external validations, the best model achieved R2 of 0.75 and 0.73 and root mean square error (RMSE) of 0.66 and 0.69 for the training and test sets, respectively. With the inherent time-consuming efforts of working with natural products (NPs), we conceived a new NP drug hit discovery strategy that consists in frontloading samples with 1D NMR descriptors to predict compounds with anticancer activity prior to bioactivity screening for NPs discovery, approach B. The NMR QSAR classification models were built using 1D NMR data (1H and13C) as descriptors, from 50 crude extracts, 55 fractions and five pure compounds obtained from actinobacteria isolated from marine sediments collected off the Madeira Archipelago. The overall predictability accuracies of the best model exceeded 63% for both training and test sets.LAQV@REQUIMTEDQ - Departamento de QuímicaUCIBIO - Applied Molecular Biosciences UnitDCV - Departamento de Ciências da VidaRUNCruz, SaraGomes, Sofia E.Borralho, Pedro M.Rodrigues, Cecília M. P.Gaudêncio, Susana P.Pereira, Florbela2019-01-29T23:44:48Z2018-09-012018-09-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttps://doi.org/10.3390/biom8030056eng2218-273XPURE: 5704499http://www.scopus.com/inward/record.url?scp=85050362659&partnerID=8YFLogxKhttps://doi.org/10.3390/biom8030056info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2024-03-11T04:28:22Zoai:run.unl.pt:10362/59003Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-20T03:33:19.378041Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse |
dc.title.none.fl_str_mv |
In silico HCT116 human colon cancer cell-based models en route to the discovery of lead-like anticancer drugs |
title |
In silico HCT116 human colon cancer cell-based models en route to the discovery of lead-like anticancer drugs |
spellingShingle |
In silico HCT116 human colon cancer cell-based models en route to the discovery of lead-like anticancer drugs Cruz, Sara Anticancer activity HCT116 cell line Machine learning (ML) Marine natural products (MNPs) Marine-derived actinobacteria Molecular descriptors NMR descriptors Quantitative structure-Activity relationship (QSAR) Biochemistry Molecular Biology SDG 3 - Good Health and Well-being SDG 14 - Life Below Water |
title_short |
In silico HCT116 human colon cancer cell-based models en route to the discovery of lead-like anticancer drugs |
title_full |
In silico HCT116 human colon cancer cell-based models en route to the discovery of lead-like anticancer drugs |
title_fullStr |
In silico HCT116 human colon cancer cell-based models en route to the discovery of lead-like anticancer drugs |
title_full_unstemmed |
In silico HCT116 human colon cancer cell-based models en route to the discovery of lead-like anticancer drugs |
title_sort |
In silico HCT116 human colon cancer cell-based models en route to the discovery of lead-like anticancer drugs |
author |
Cruz, Sara |
author_facet |
Cruz, Sara Gomes, Sofia E. Borralho, Pedro M. Rodrigues, Cecília M. P. Gaudêncio, Susana P. Pereira, Florbela |
author_role |
author |
author2 |
Gomes, Sofia E. Borralho, Pedro M. Rodrigues, Cecília M. P. Gaudêncio, Susana P. Pereira, Florbela |
author2_role |
author author author author author |
dc.contributor.none.fl_str_mv |
LAQV@REQUIMTE DQ - Departamento de Química UCIBIO - Applied Molecular Biosciences Unit DCV - Departamento de Ciências da Vida RUN |
dc.contributor.author.fl_str_mv |
Cruz, Sara Gomes, Sofia E. Borralho, Pedro M. Rodrigues, Cecília M. P. Gaudêncio, Susana P. Pereira, Florbela |
dc.subject.por.fl_str_mv |
Anticancer activity HCT116 cell line Machine learning (ML) Marine natural products (MNPs) Marine-derived actinobacteria Molecular descriptors NMR descriptors Quantitative structure-Activity relationship (QSAR) Biochemistry Molecular Biology SDG 3 - Good Health and Well-being SDG 14 - Life Below Water |
topic |
Anticancer activity HCT116 cell line Machine learning (ML) Marine natural products (MNPs) Marine-derived actinobacteria Molecular descriptors NMR descriptors Quantitative structure-Activity relationship (QSAR) Biochemistry Molecular Biology SDG 3 - Good Health and Well-being SDG 14 - Life Below Water |
description |
Financial support from Fundacao para a Ciencia e Tecnologia (FCT) Portugal, under Project PTDC/QUIQUI/119116/2010 and grants SFRH/BPD/108237/2015 (F.P.) and IF/00700/2014 (S.P.G.) are greatly appreciated. This work was also supported by the LAQV and UCIBIO, which are financed by national funds from FCT/MEC (UID/QUI/50006/2013 and UID/Multi/04378/2013), respectively) and co-financed by the ERDF under the PT2020 Partnership Agreement (POCI-01-0145-FEDER-007265 and POCI-010145-FEDER-007728, respectively), and by Programme grant SAICTPAC/0019/2015 funded by European Structural and Investment Funds through the COMPETE Programme and by National Funds through FCT. The NMR spectrometers are part of The National NMR Facility, supported by FCT (RECI/BBB-BQB/0230/2012). |
publishDate |
2018 |
dc.date.none.fl_str_mv |
2018-09-01 2018-09-01T00:00:00Z 2019-01-29T23:44:48Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
https://doi.org/10.3390/biom8030056 |
url |
https://doi.org/10.3390/biom8030056 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
2218-273X PURE: 5704499 http://www.scopus.com/inward/record.url?scp=85050362659&partnerID=8YFLogxK https://doi.org/10.3390/biom8030056 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.source.none.fl_str_mv |
reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação instacron:RCAAP |
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Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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RCAAP |
institution |
RCAAP |
reponame_str |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
repository.name.fl_str_mv |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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1799137955160260608 |