A selective p53 activator and anticancer agent to improve colorectal cancer therapy

Detalhes bibliográficos
Autor(a) principal: Ramos, Helena
Data de Publicação: 2021
Outros Autores: Soares, Maria I. L., Silva, Joana, Raimundo, Liliana, Calheiros, Juliana, Gomes, Célia, Reis, Flávio, Monteiro, Filipe A., Nunes, Cláudia, Reis, Salette, Bosco, Bartolomeo, Piazza, Silvano, Domingues, Lucília, Chlapek, Petr, Vlcek, Petr, Fabian, Pavel, Rajado, Ana Teresa, Carvalho, A. T. P., Veselska, Renata, Inga, Alberto, Melo, Teresa M. V. D. Pinho e, Saraiva, Lucília
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10316/103826
https://doi.org/10.1016/j.celrep.2021.108982
Resumo: Impairment of the p53 pathway is a critical event in cancer. Therefore, reestablishing p53 activity has become one of the most appealing anticancer therapeutic strategies. Here, we disclose the p53-activating anticancer drug (3S)-6,7-bis(hydroxymethyl)-5-methyl-3-phenyl-1H,3H-pyrrolo[1,2-c]thiazole (MANIO). MANIO demonstrates a notable selectivity to the p53 pathway, activating wild-type (WT)p53 and restoring WT-like function to mutant (mut)p53 in human cancer cells. MANIO directly binds to the WT/mutp53 DNA-binding domain, enhancing the protein thermal stability, DNA-binding ability, and transcriptional activity. The high efficacy of MANIO as an anticancer agent toward cancers harboring WT/mutp53 is further demonstrated in patient-derived cells and xenograft mouse models of colorectal cancer (CRC), with no signs of undesirable side effects. MANIO synergizes with conventional chemotherapeutic drugs, and in vitro and in vivo studies predict its adequate drug-likeness and pharmacokinetic properties for a clinical candidate. As a single agent or in combination, MANIO will advance anticancer-targeted therapy, particularly benefiting CRC patients harboring distinct p53 status.
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spelling A selective p53 activator and anticancer agent to improve colorectal cancer therapyanticancer drug; colorectal cancer; p53 activator; targeted therapyAnimalsAntineoplastic AgentsAntineoplastic Combined Chemotherapy ProtocolsApoptosisCell Cycle CheckpointsCell Line, TumorCell ProliferationCisplatinColorectal NeoplasmsDoxorubicinDrug DiscoveryDrug SynergismFemaleFluorouracilGene Expression Regulation, NeoplasticHCT116 CellsHumansMiceMice, NudeProtein BindingPyrrolesThiazolesTumor Suppressor Protein p53Xenograft Model Antitumor AssaysImpairment of the p53 pathway is a critical event in cancer. Therefore, reestablishing p53 activity has become one of the most appealing anticancer therapeutic strategies. Here, we disclose the p53-activating anticancer drug (3S)-6,7-bis(hydroxymethyl)-5-methyl-3-phenyl-1H,3H-pyrrolo[1,2-c]thiazole (MANIO). MANIO demonstrates a notable selectivity to the p53 pathway, activating wild-type (WT)p53 and restoring WT-like function to mutant (mut)p53 in human cancer cells. MANIO directly binds to the WT/mutp53 DNA-binding domain, enhancing the protein thermal stability, DNA-binding ability, and transcriptional activity. The high efficacy of MANIO as an anticancer agent toward cancers harboring WT/mutp53 is further demonstrated in patient-derived cells and xenograft mouse models of colorectal cancer (CRC), with no signs of undesirable side effects. MANIO synergizes with conventional chemotherapeutic drugs, and in vitro and in vivo studies predict its adequate drug-likeness and pharmacokinetic properties for a clinical candidate. As a single agent or in combination, MANIO will advance anticancer-targeted therapy, particularly benefiting CRC patients harboring distinct p53 status.Elsevier2021-04-13info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://hdl.handle.net/10316/103826http://hdl.handle.net/10316/103826https://doi.org/10.1016/j.celrep.2021.108982eng22111247Ramos, HelenaSoares, Maria I. L.Silva, JoanaRaimundo, LilianaCalheiros, JulianaGomes, CéliaReis, FlávioMonteiro, Filipe A.Nunes, CláudiaReis, SaletteBosco, BartolomeoPiazza, SilvanoDomingues, LucíliaChlapek, PetrVlcek, PetrFabian, PavelRajado, Ana TeresaCarvalho, A. T. P.Veselska, RenataInga, AlbertoMelo, Teresa M. V. D. Pinho eSaraiva, Lucíliainfo: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:RCAAP2022-11-30T21:38:41Zoai:estudogeral.uc.pt:10316/103826Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T21:20:35.839462Repositório 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 A selective p53 activator and anticancer agent to improve colorectal cancer therapy
title A selective p53 activator and anticancer agent to improve colorectal cancer therapy
spellingShingle A selective p53 activator and anticancer agent to improve colorectal cancer therapy
Ramos, Helena
anticancer drug; colorectal cancer; p53 activator; targeted therapy
Animals
Antineoplastic Agents
Antineoplastic Combined Chemotherapy Protocols
Apoptosis
Cell Cycle Checkpoints
Cell Line, Tumor
Cell Proliferation
Cisplatin
Colorectal Neoplasms
Doxorubicin
Drug Discovery
Drug Synergism
Female
Fluorouracil
Gene Expression Regulation, Neoplastic
HCT116 Cells
Humans
Mice
Mice, Nude
Protein Binding
Pyrroles
Thiazoles
Tumor Suppressor Protein p53
Xenograft Model Antitumor Assays
title_short A selective p53 activator and anticancer agent to improve colorectal cancer therapy
title_full A selective p53 activator and anticancer agent to improve colorectal cancer therapy
title_fullStr A selective p53 activator and anticancer agent to improve colorectal cancer therapy
title_full_unstemmed A selective p53 activator and anticancer agent to improve colorectal cancer therapy
title_sort A selective p53 activator and anticancer agent to improve colorectal cancer therapy
author Ramos, Helena
author_facet Ramos, Helena
Soares, Maria I. L.
Silva, Joana
Raimundo, Liliana
Calheiros, Juliana
Gomes, Célia
Reis, Flávio
Monteiro, Filipe A.
Nunes, Cláudia
Reis, Salette
Bosco, Bartolomeo
Piazza, Silvano
Domingues, Lucília
Chlapek, Petr
Vlcek, Petr
Fabian, Pavel
Rajado, Ana Teresa
Carvalho, A. T. P.
Veselska, Renata
Inga, Alberto
Melo, Teresa M. V. D. Pinho e
Saraiva, Lucília
author_role author
author2 Soares, Maria I. L.
Silva, Joana
Raimundo, Liliana
Calheiros, Juliana
Gomes, Célia
Reis, Flávio
Monteiro, Filipe A.
Nunes, Cláudia
Reis, Salette
Bosco, Bartolomeo
Piazza, Silvano
Domingues, Lucília
Chlapek, Petr
Vlcek, Petr
Fabian, Pavel
Rajado, Ana Teresa
Carvalho, A. T. P.
Veselska, Renata
Inga, Alberto
Melo, Teresa M. V. D. Pinho e
Saraiva, Lucília
author2_role author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Ramos, Helena
Soares, Maria I. L.
Silva, Joana
Raimundo, Liliana
Calheiros, Juliana
Gomes, Célia
Reis, Flávio
Monteiro, Filipe A.
Nunes, Cláudia
Reis, Salette
Bosco, Bartolomeo
Piazza, Silvano
Domingues, Lucília
Chlapek, Petr
Vlcek, Petr
Fabian, Pavel
Rajado, Ana Teresa
Carvalho, A. T. P.
Veselska, Renata
Inga, Alberto
Melo, Teresa M. V. D. Pinho e
Saraiva, Lucília
dc.subject.por.fl_str_mv anticancer drug; colorectal cancer; p53 activator; targeted therapy
Animals
Antineoplastic Agents
Antineoplastic Combined Chemotherapy Protocols
Apoptosis
Cell Cycle Checkpoints
Cell Line, Tumor
Cell Proliferation
Cisplatin
Colorectal Neoplasms
Doxorubicin
Drug Discovery
Drug Synergism
Female
Fluorouracil
Gene Expression Regulation, Neoplastic
HCT116 Cells
Humans
Mice
Mice, Nude
Protein Binding
Pyrroles
Thiazoles
Tumor Suppressor Protein p53
Xenograft Model Antitumor Assays
topic anticancer drug; colorectal cancer; p53 activator; targeted therapy
Animals
Antineoplastic Agents
Antineoplastic Combined Chemotherapy Protocols
Apoptosis
Cell Cycle Checkpoints
Cell Line, Tumor
Cell Proliferation
Cisplatin
Colorectal Neoplasms
Doxorubicin
Drug Discovery
Drug Synergism
Female
Fluorouracil
Gene Expression Regulation, Neoplastic
HCT116 Cells
Humans
Mice
Mice, Nude
Protein Binding
Pyrroles
Thiazoles
Tumor Suppressor Protein p53
Xenograft Model Antitumor Assays
description Impairment of the p53 pathway is a critical event in cancer. Therefore, reestablishing p53 activity has become one of the most appealing anticancer therapeutic strategies. Here, we disclose the p53-activating anticancer drug (3S)-6,7-bis(hydroxymethyl)-5-methyl-3-phenyl-1H,3H-pyrrolo[1,2-c]thiazole (MANIO). MANIO demonstrates a notable selectivity to the p53 pathway, activating wild-type (WT)p53 and restoring WT-like function to mutant (mut)p53 in human cancer cells. MANIO directly binds to the WT/mutp53 DNA-binding domain, enhancing the protein thermal stability, DNA-binding ability, and transcriptional activity. The high efficacy of MANIO as an anticancer agent toward cancers harboring WT/mutp53 is further demonstrated in patient-derived cells and xenograft mouse models of colorectal cancer (CRC), with no signs of undesirable side effects. MANIO synergizes with conventional chemotherapeutic drugs, and in vitro and in vivo studies predict its adequate drug-likeness and pharmacokinetic properties for a clinical candidate. As a single agent or in combination, MANIO will advance anticancer-targeted therapy, particularly benefiting CRC patients harboring distinct p53 status.
publishDate 2021
dc.date.none.fl_str_mv 2021-04-13
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 http://hdl.handle.net/10316/103826
http://hdl.handle.net/10316/103826
https://doi.org/10.1016/j.celrep.2021.108982
url http://hdl.handle.net/10316/103826
https://doi.org/10.1016/j.celrep.2021.108982
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 22111247
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
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dc.publisher.none.fl_str_mv Elsevier
publisher.none.fl_str_mv Elsevier
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