Alterations in PTEN, MDM2, TP53 and AR protein and gene expression are associated with canine prostate carcinogenesis
Autor(a) principal: | |
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Data de Publicação: | 2016 |
Outros Autores: | , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
Texto Completo: | http://dx.doi.org/10.1016/j.rvsc.2016.03.008 http://hdl.handle.net/11449/172719 |
Resumo: | The PTEN, AR, MDM2 and p53 protein network plays a central role in the development of many human cancers, thus eliciting the development of targeted cancer therapeutics. Dogs spontaneously develop tumours, and they are considered a good model for comparative oncology initiatives. Due to the limited information on these proteins in canine tumours, this study aimed to investigate gene and protein alterations in PTEN, AR, MDM2 and p53 in canine prostate cancer (PC). Protein expression was evaluated by immunohistochemistry (15 normal, 22 proliferative inflammatory atrophy (PIA) and 19 PC samples) and Western blotting (2 normal prostate tissue, 2 BPH, 2 PIA samples and 2 PC samples) and gene expression by RT-qPCR (10 normal, 10 PIA and 15 PC samples) of formalin-fixed tissue. We identified nuclear and cytoplasmic expression of PTEN and p53 in all samples, with only nuclear staining found for MDM2 and AR. Our results revealed high expression of MDM2 in PC and PIA samples compared to normal samples, whereas PTEN, P53 and AR expression was down-regulated in PC compared to normal tissue. All tumour samples (n = 19) showed loss of nuclear PTEN expression, and all cancer mimickers showed positive nuclear staining. Therefore, nuclear PTEN staining could be a good diagnostic marker for differentiating between malignant lesions and mimickers. Canine prostate carcinogenesis involves increased expression of MDM2 in association with decreased expression of PTEN, p53 and AR, such as occurs in hormone refractory PC in men. Thus, dogs may be an important model for studying advanced stage PC. |
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Alterations in PTEN, MDM2, TP53 and AR protein and gene expression are associated with canine prostate carcinogenesisDogFormalin-fixed tissueGene expressionImmunohistochemistryProstatic diseaseThe PTEN, AR, MDM2 and p53 protein network plays a central role in the development of many human cancers, thus eliciting the development of targeted cancer therapeutics. Dogs spontaneously develop tumours, and they are considered a good model for comparative oncology initiatives. Due to the limited information on these proteins in canine tumours, this study aimed to investigate gene and protein alterations in PTEN, AR, MDM2 and p53 in canine prostate cancer (PC). Protein expression was evaluated by immunohistochemistry (15 normal, 22 proliferative inflammatory atrophy (PIA) and 19 PC samples) and Western blotting (2 normal prostate tissue, 2 BPH, 2 PIA samples and 2 PC samples) and gene expression by RT-qPCR (10 normal, 10 PIA and 15 PC samples) of formalin-fixed tissue. We identified nuclear and cytoplasmic expression of PTEN and p53 in all samples, with only nuclear staining found for MDM2 and AR. Our results revealed high expression of MDM2 in PC and PIA samples compared to normal samples, whereas PTEN, P53 and AR expression was down-regulated in PC compared to normal tissue. All tumour samples (n = 19) showed loss of nuclear PTEN expression, and all cancer mimickers showed positive nuclear staining. Therefore, nuclear PTEN staining could be a good diagnostic marker for differentiating between malignant lesions and mimickers. Canine prostate carcinogenesis involves increased expression of MDM2 in association with decreased expression of PTEN, p53 and AR, such as occurs in hormone refractory PC in men. Thus, dogs may be an important model for studying advanced stage PC.Faculdade de Ciências Agronômicas Univ. Estadual Paulista - UNESPDepartment of Veterinary Clinic School of Veterinary Medicine and Animal Science Univ. Estadual Paulista - UNESPDepartment of Urology Botucatu Medical School - FMB Univ. Estadual Paulista - UNESPFaculdade de Ciências Agronômicas Univ. Estadual Paulista - UNESPDepartment of Veterinary Clinic School of Veterinary Medicine and Animal Science Univ. Estadual Paulista - UNESPDepartment of Urology Botucatu Medical School - FMB Univ. Estadual Paulista - UNESPUniversidade Estadual Paulista (Unesp)Rivera-Calderón, Luis Gabriel [UNESP]Fonseca-Alves, Carlos Eduardo [UNESP]Kobayashi, Priscila Emiko [UNESP]Carvalho, Marcio [UNESP]Drigo, Sandra Aparecida [UNESP]de Oliveira Vasconcelos, Rosemeri [UNESP]Laufer-Amorim, Renée [UNESP]2018-12-11T17:01:54Z2018-12-11T17:01:54Z2016-06-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article56-61application/pdfhttp://dx.doi.org/10.1016/j.rvsc.2016.03.008Research in Veterinary Science, v. 106, p. 56-61.1532-26610034-5288http://hdl.handle.net/11449/17271910.1016/j.rvsc.2016.03.0082-s2.0-849612562362-s2.0-84961256236.pdfScopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengResearch in Veterinary Science0,593info:eu-repo/semantics/openAccess2024-09-03T14:29:56Zoai:repositorio.unesp.br:11449/172719Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestrepositoriounesp@unesp.bropendoar:29462024-09-03T14:29:56Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
Alterations in PTEN, MDM2, TP53 and AR protein and gene expression are associated with canine prostate carcinogenesis |
title |
Alterations in PTEN, MDM2, TP53 and AR protein and gene expression are associated with canine prostate carcinogenesis |
spellingShingle |
Alterations in PTEN, MDM2, TP53 and AR protein and gene expression are associated with canine prostate carcinogenesis Rivera-Calderón, Luis Gabriel [UNESP] Dog Formalin-fixed tissue Gene expression Immunohistochemistry Prostatic disease |
title_short |
Alterations in PTEN, MDM2, TP53 and AR protein and gene expression are associated with canine prostate carcinogenesis |
title_full |
Alterations in PTEN, MDM2, TP53 and AR protein and gene expression are associated with canine prostate carcinogenesis |
title_fullStr |
Alterations in PTEN, MDM2, TP53 and AR protein and gene expression are associated with canine prostate carcinogenesis |
title_full_unstemmed |
Alterations in PTEN, MDM2, TP53 and AR protein and gene expression are associated with canine prostate carcinogenesis |
title_sort |
Alterations in PTEN, MDM2, TP53 and AR protein and gene expression are associated with canine prostate carcinogenesis |
author |
Rivera-Calderón, Luis Gabriel [UNESP] |
author_facet |
Rivera-Calderón, Luis Gabriel [UNESP] Fonseca-Alves, Carlos Eduardo [UNESP] Kobayashi, Priscila Emiko [UNESP] Carvalho, Marcio [UNESP] Drigo, Sandra Aparecida [UNESP] de Oliveira Vasconcelos, Rosemeri [UNESP] Laufer-Amorim, Renée [UNESP] |
author_role |
author |
author2 |
Fonseca-Alves, Carlos Eduardo [UNESP] Kobayashi, Priscila Emiko [UNESP] Carvalho, Marcio [UNESP] Drigo, Sandra Aparecida [UNESP] de Oliveira Vasconcelos, Rosemeri [UNESP] Laufer-Amorim, Renée [UNESP] |
author2_role |
author author author author author author |
dc.contributor.none.fl_str_mv |
Universidade Estadual Paulista (Unesp) |
dc.contributor.author.fl_str_mv |
Rivera-Calderón, Luis Gabriel [UNESP] Fonseca-Alves, Carlos Eduardo [UNESP] Kobayashi, Priscila Emiko [UNESP] Carvalho, Marcio [UNESP] Drigo, Sandra Aparecida [UNESP] de Oliveira Vasconcelos, Rosemeri [UNESP] Laufer-Amorim, Renée [UNESP] |
dc.subject.por.fl_str_mv |
Dog Formalin-fixed tissue Gene expression Immunohistochemistry Prostatic disease |
topic |
Dog Formalin-fixed tissue Gene expression Immunohistochemistry Prostatic disease |
description |
The PTEN, AR, MDM2 and p53 protein network plays a central role in the development of many human cancers, thus eliciting the development of targeted cancer therapeutics. Dogs spontaneously develop tumours, and they are considered a good model for comparative oncology initiatives. Due to the limited information on these proteins in canine tumours, this study aimed to investigate gene and protein alterations in PTEN, AR, MDM2 and p53 in canine prostate cancer (PC). Protein expression was evaluated by immunohistochemistry (15 normal, 22 proliferative inflammatory atrophy (PIA) and 19 PC samples) and Western blotting (2 normal prostate tissue, 2 BPH, 2 PIA samples and 2 PC samples) and gene expression by RT-qPCR (10 normal, 10 PIA and 15 PC samples) of formalin-fixed tissue. We identified nuclear and cytoplasmic expression of PTEN and p53 in all samples, with only nuclear staining found for MDM2 and AR. Our results revealed high expression of MDM2 in PC and PIA samples compared to normal samples, whereas PTEN, P53 and AR expression was down-regulated in PC compared to normal tissue. All tumour samples (n = 19) showed loss of nuclear PTEN expression, and all cancer mimickers showed positive nuclear staining. Therefore, nuclear PTEN staining could be a good diagnostic marker for differentiating between malignant lesions and mimickers. Canine prostate carcinogenesis involves increased expression of MDM2 in association with decreased expression of PTEN, p53 and AR, such as occurs in hormone refractory PC in men. Thus, dogs may be an important model for studying advanced stage PC. |
publishDate |
2016 |
dc.date.none.fl_str_mv |
2016-06-01 2018-12-11T17:01:54Z 2018-12-11T17:01:54Z |
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://dx.doi.org/10.1016/j.rvsc.2016.03.008 Research in Veterinary Science, v. 106, p. 56-61. 1532-2661 0034-5288 http://hdl.handle.net/11449/172719 10.1016/j.rvsc.2016.03.008 2-s2.0-84961256236 2-s2.0-84961256236.pdf |
url |
http://dx.doi.org/10.1016/j.rvsc.2016.03.008 http://hdl.handle.net/11449/172719 |
identifier_str_mv |
Research in Veterinary Science, v. 106, p. 56-61. 1532-2661 0034-5288 10.1016/j.rvsc.2016.03.008 2-s2.0-84961256236 2-s2.0-84961256236.pdf |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Research in Veterinary Science 0,593 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
56-61 application/pdf |
dc.source.none.fl_str_mv |
Scopus reponame:Repositório Institucional da UNESP instname:Universidade Estadual Paulista (UNESP) instacron:UNESP |
instname_str |
Universidade Estadual Paulista (UNESP) |
instacron_str |
UNESP |
institution |
UNESP |
reponame_str |
Repositório Institucional da UNESP |
collection |
Repositório Institucional da UNESP |
repository.name.fl_str_mv |
Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP) |
repository.mail.fl_str_mv |
repositoriounesp@unesp.br |
_version_ |
1810021363539247104 |