Tracking prostate carcinogenesis over time through urine proteome profiling in an animal model: an exploratory approach
Autor(a) principal: | |
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Data de Publicação: | 2022 |
Outros Autores: | , , , , , , , , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
Texto Completo: | http://hdl.handle.net/10400.1/18105 |
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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Tracking prostate carcinogenesis over time through urine proteome profiling in an animal model: an exploratory approachAgingGeLC-MS/MSUrinary proteomicsProstate adenocarcinomaRetinol-binding protein 4Cadherin-2Enolase-1Prostate 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.CEECIND/03935/2021MDPISapientiaMoreira-Pais, AlexandraNogueira-Ferreira, RitaReis, StephanieAveiro, SusanaBarros, AntónioMelo, TâniaMatos, BárbaraDuarte, José AlbertoSeixas, FernandaDomingues, PedroAmado, FranciscoFardilha, MargaridaOliveira, Paula A.Ferreira, RitaVitorino, Rui2022-07-27T09:20:15Z2022-07-082022-07-25T16:32:52Z2022-07-08T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.1/18105engInternational Journal of Molecular Sciences 23 (14): 7560 (2022)10.3390/ijms231475601422-0067info: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:RCAAP2024-03-13T02:07:45Zoai:sapientia.ualg.pt:10400.1/18105Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T20:07:54.198718Repositório 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 GeLC-MS/MS Urinary proteomics Prostate adenocarcinoma Retinol-binding protein 4 Cadherin-2 Enolase-1 |
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.none.fl_str_mv |
Sapientia |
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 GeLC-MS/MS Urinary proteomics Prostate adenocarcinoma Retinol-binding protein 4 Cadherin-2 Enolase-1 |
topic |
Aging GeLC-MS/MS Urinary proteomics Prostate adenocarcinoma Retinol-binding protein 4 Cadherin-2 Enolase-1 |
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 |
2022-07-27T09:20:15Z 2022-07-08 2022-07-25T16:32:52Z 2022-07-08T00:00:00Z |
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/10400.1/18105 |
url |
http://hdl.handle.net/10400.1/18105 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
International Journal of Molecular Sciences 23 (14): 7560 (2022) 10.3390/ijms23147560 1422-0067 |
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.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 |
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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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1799133324439977984 |