Tracking Prostate Carcinogenesis over Time through Urine Proteome Profiling in an Animal Model: An Exploratory Approach

Detalhes bibliográficos
Autor(a) principal: Moreira-Pais, Alexandra
Data de Publicação: 2022
Outros Autores: Nogueira-Ferreira, Rita, Reis, Stephanie, Aveiro, Susana, Barros, António, Melo, Tânia, Matos, Bárbara, Duarte, José Alberto, Seixas, Fernanda, Domingues, Pedro, Amado, Francisco, Fardilha, Margarida, Oliveira, Paula A, Ferreira, Rita, Vitorino, Rui
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10773/40037
Resumo: Prostate cancer (PCa) is one of the most lethal diseases in men, which justifies the search for new diagnostic tools. The aim of the present study was to gain new insights into the progression of prostate carcinogenesis by analyzing the urine proteome. To this end, urine from healthy animals and animals with prostate adenocarcinoma was analyzed at two time points: 27 and 54 weeks. After 54 weeks, the incidence of pre-neoplastic and neoplastic lesions in the PCa animals was 100%. GeLC-MS/MS and subsequent bioinformatics analyses revealed several proteins involved in prostate carcinogenesis. Increased levels of retinol-binding protein 4 and decreased levels of cadherin-2 appear to be characteristic of early stages of the disease, whereas increased levels of enolase-1 and T-kininogen 2 and decreased levels of isocitrate dehydrogenase 2 describe more advanced stages. With increasing age, urinary levels of clusterin and corticosteroid-binding globulin increased and neprilysin levels decreased, all of which appear to play a role in prostate hyperplasia or carcinogenesis. The present exploratory analysis can be considered as a starting point for studies targeting specific human urine proteins for early detection of age-related maladaptive changes in the prostate that may lead to cancer.
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spelling Tracking Prostate Carcinogenesis over Time through Urine Proteome Profiling in an Animal Model: An Exploratory ApproachAging; cadherin-2Enolase-1GeLC-MS/MSProstate adenocarcinomaRetinol-binding protein 4Urinary proteomicsProstate cancer (PCa) is one of the most lethal diseases in men, which justifies the search for new diagnostic tools. The aim of the present study was to gain new insights into the progression of prostate carcinogenesis by analyzing the urine proteome. To this end, urine from healthy animals and animals with prostate adenocarcinoma was analyzed at two time points: 27 and 54 weeks. After 54 weeks, the incidence of pre-neoplastic and neoplastic lesions in the PCa animals was 100%. GeLC-MS/MS and subsequent bioinformatics analyses revealed several proteins involved in prostate carcinogenesis. Increased levels of retinol-binding protein 4 and decreased levels of cadherin-2 appear to be characteristic of early stages of the disease, whereas increased levels of enolase-1 and T-kininogen 2 and decreased levels of isocitrate dehydrogenase 2 describe more advanced stages. With increasing age, urinary levels of clusterin and corticosteroid-binding globulin increased and neprilysin levels decreased, all of which appear to play a role in prostate hyperplasia or carcinogenesis. The present exploratory analysis can be considered as a starting point for studies targeting specific human urine proteins for early detection of age-related maladaptive changes in the prostate that may lead to cancer.MDPI2024-01-10T11:16:29Z2022-07-08T00:00:00Z2022-07-08info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10773/40037eng1661-659610.3390/ijms23147560Moreira-Pais, AlexandraNogueira-Ferreira, RitaReis, StephanieAveiro, SusanaBarros, AntónioMelo, TâniaMatos, BárbaraDuarte, José AlbertoSeixas, FernandaDomingues, PedroAmado, FranciscoFardilha, MargaridaOliveira, Paula AFerreira, RitaVitorino, Ruiinfo: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:RCAAP2024-02-22T12:18:13Zoai:ria.ua.pt:10773/40037Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-20T03:10:04.154488Repositório 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 Tracking Prostate Carcinogenesis over Time through Urine Proteome Profiling in an Animal Model: An Exploratory Approach
title Tracking Prostate Carcinogenesis over Time through Urine Proteome Profiling in an Animal Model: An Exploratory Approach
spellingShingle Tracking Prostate Carcinogenesis over Time through Urine Proteome Profiling in an Animal Model: An Exploratory Approach
Moreira-Pais, Alexandra
Aging; cadherin-2
Enolase-1
GeLC-MS/MS
Prostate adenocarcinoma
Retinol-binding protein 4
Urinary proteomics
title_short Tracking Prostate Carcinogenesis over Time through Urine Proteome Profiling in an Animal Model: An Exploratory Approach
title_full Tracking Prostate Carcinogenesis over Time through Urine Proteome Profiling in an Animal Model: An Exploratory Approach
title_fullStr Tracking Prostate Carcinogenesis over Time through Urine Proteome Profiling in an Animal Model: An Exploratory Approach
title_full_unstemmed Tracking Prostate Carcinogenesis over Time through Urine Proteome Profiling in an Animal Model: An Exploratory Approach
title_sort Tracking Prostate Carcinogenesis over Time through Urine Proteome Profiling in an Animal Model: An Exploratory Approach
author Moreira-Pais, Alexandra
author_facet Moreira-Pais, Alexandra
Nogueira-Ferreira, Rita
Reis, Stephanie
Aveiro, Susana
Barros, António
Melo, Tânia
Matos, Bárbara
Duarte, José Alberto
Seixas, Fernanda
Domingues, Pedro
Amado, Francisco
Fardilha, Margarida
Oliveira, Paula A
Ferreira, Rita
Vitorino, Rui
author_role author
author2 Nogueira-Ferreira, Rita
Reis, Stephanie
Aveiro, Susana
Barros, António
Melo, Tânia
Matos, Bárbara
Duarte, José Alberto
Seixas, Fernanda
Domingues, Pedro
Amado, Francisco
Fardilha, Margarida
Oliveira, Paula A
Ferreira, Rita
Vitorino, Rui
author2_role author
author
author
author
author
author
author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Moreira-Pais, Alexandra
Nogueira-Ferreira, Rita
Reis, Stephanie
Aveiro, Susana
Barros, António
Melo, Tânia
Matos, Bárbara
Duarte, José Alberto
Seixas, Fernanda
Domingues, Pedro
Amado, Francisco
Fardilha, Margarida
Oliveira, Paula A
Ferreira, Rita
Vitorino, Rui
dc.subject.por.fl_str_mv Aging; cadherin-2
Enolase-1
GeLC-MS/MS
Prostate adenocarcinoma
Retinol-binding protein 4
Urinary proteomics
topic Aging; cadherin-2
Enolase-1
GeLC-MS/MS
Prostate adenocarcinoma
Retinol-binding protein 4
Urinary proteomics
description Prostate cancer (PCa) is one of the most lethal diseases in men, which justifies the search for new diagnostic tools. The aim of the present study was to gain new insights into the progression of prostate carcinogenesis by analyzing the urine proteome. To this end, urine from healthy animals and animals with prostate adenocarcinoma was analyzed at two time points: 27 and 54 weeks. After 54 weeks, the incidence of pre-neoplastic and neoplastic lesions in the PCa animals was 100%. GeLC-MS/MS and subsequent bioinformatics analyses revealed several proteins involved in prostate carcinogenesis. Increased levels of retinol-binding protein 4 and decreased levels of cadherin-2 appear to be characteristic of early stages of the disease, whereas increased levels of enolase-1 and T-kininogen 2 and decreased levels of isocitrate dehydrogenase 2 describe more advanced stages. With increasing age, urinary levels of clusterin and corticosteroid-binding globulin increased and neprilysin levels decreased, all of which appear to play a role in prostate hyperplasia or carcinogenesis. The present exploratory analysis can be considered as a starting point for studies targeting specific human urine proteins for early detection of age-related maladaptive changes in the prostate that may lead to cancer.
publishDate 2022
dc.date.none.fl_str_mv 2022-07-08T00:00:00Z
2022-07-08
2024-01-10T11:16:29Z
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/10773/40037
url http://hdl.handle.net/10773/40037
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 1661-6596
10.3390/ijms23147560
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
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dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv MDPI
publisher.none.fl_str_mv MDPI
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
instname_str Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron_str RCAAP
institution RCAAP
reponame_str Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
collection 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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