The investigation of transcriptional repression mediated by ZEB2 in canine invasive micropapillary carcinoma in mammary gland

Detalhes bibliográficos
Autor(a) principal: Conrado de Oliveira Gamba
Data de Publicação: 2019
Outros Autores: Karine Araújo Damasceno, Izabel Cristina Ferreira, Michele Angela Rodrigues, Dawidson Assis Gomes, Mariana Resende Alves, Rafael Malagoli Rocha, Alessandra Estrela Lima, Enio Ferreira, Geovanni Dantas Cassali
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UFMG
Texto Completo: https://doi.org/10.1371/journal.pone.0209497
http://hdl.handle.net/1843/56451
https://orcid.org/0000-0002-2035-8961
https://orcid.org/0000-0003-2087-1690
https://orcid.org/0000-0002-0233-7729
https://orcid.org/0000-0001-7714-991X
http://orcid.org/0000-0001-5904-4890
https://orcid.org/0000-0002-9879-7999
https://orcid.org/0000-0002-1835-0303
http://orcid.org/0000-0002-5650-6743
Resumo: The E-cadherin loss has frequently been associated with transcriptional repression mediated by transcription factors, such as the Zinc Finger E-Box Binding Homeobox-2 (ZEB2). Invasive micropapillary carcinomas (IMPCs) of the breast are aggressive neoplasms frequently related to lymph node metastasis and poor overall survival. In the canine mammary gland, IMPCs has just been reported and, based on its behavioral similarity with the human IMPCs, appears to be a good spontaneous model to this human entity. This study aimed to evaluate the relationship between E-cadherin and ZEB2 in a spontaneous canine model of invasive micropapillary carcinoma of the mammary gland. The correlation among gene expression (ZEB2 and CDH1) and clinicopathological findings was also explored. Nineteen cases of IMPC of the canine mammary gland were obtained, protein and mRNA expression were investigated through immunohistochemistry and RNA In Situ Hybridization, respectively. To better understand the relationship between E-cadherin and ZEB2, immunofluorescence was performed in canine IMPCs. Immunohistochemically, most of IMPCs showed 1+ (14/19, 73.7%) for E-cadherin; and positivity for ZEB2 was diagnosed in 47.4% of the IMPCs. Regarding the RNA In Situ Hybridization (ISH), most of IMPCs showed 4+ and 0+ for E-cadherin (CDH1) and ZEB2 respectively. Through immunofluorescence, the first and second more frequent combinatorial group were E-cadherin+ZEB2- and E-cadherin+ZEB2+; neoplastic cells showing concomitantly weak expression for E-cadherin and positivity for ZEB2 were frequently observed. A negative correlation was observed between E-cadherin and progesterone receptor expression in IMPCs. Based on these results, canine mammary IMPCs show E-cadherin lost and, at times reveals nuclear positivity for the transcription factor ZEB2 that seems to exert transcriptional repression of the CDH1.
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spelling 2023-07-17T19:01:37Z2023-07-17T19:01:37Z2019143https://doi.org/10.1371/journal.pone.02094971932-6203http://hdl.handle.net/1843/56451https://orcid.org/0000-0002-2035-8961https://orcid.org/0000-0003-2087-1690https://orcid.org/0000-0002-0233-7729https://orcid.org/0000-0001-7714-991Xhttp://orcid.org/0000-0001-5904-4890https://orcid.org/0000-0002-9879-7999https://orcid.org/0000-0002-1835-0303http://orcid.org/0000-0002-5650-6743The E-cadherin loss has frequently been associated with transcriptional repression mediated by transcription factors, such as the Zinc Finger E-Box Binding Homeobox-2 (ZEB2). Invasive micropapillary carcinomas (IMPCs) of the breast are aggressive neoplasms frequently related to lymph node metastasis and poor overall survival. In the canine mammary gland, IMPCs has just been reported and, based on its behavioral similarity with the human IMPCs, appears to be a good spontaneous model to this human entity. This study aimed to evaluate the relationship between E-cadherin and ZEB2 in a spontaneous canine model of invasive micropapillary carcinoma of the mammary gland. The correlation among gene expression (ZEB2 and CDH1) and clinicopathological findings was also explored. Nineteen cases of IMPC of the canine mammary gland were obtained, protein and mRNA expression were investigated through immunohistochemistry and RNA In Situ Hybridization, respectively. To better understand the relationship between E-cadherin and ZEB2, immunofluorescence was performed in canine IMPCs. Immunohistochemically, most of IMPCs showed 1+ (14/19, 73.7%) for E-cadherin; and positivity for ZEB2 was diagnosed in 47.4% of the IMPCs. Regarding the RNA In Situ Hybridization (ISH), most of IMPCs showed 4+ and 0+ for E-cadherin (CDH1) and ZEB2 respectively. Through immunofluorescence, the first and second more frequent combinatorial group were E-cadherin+ZEB2- and E-cadherin+ZEB2+; neoplastic cells showing concomitantly weak expression for E-cadherin and positivity for ZEB2 were frequently observed. A negative correlation was observed between E-cadherin and progesterone receptor expression in IMPCs. Based on these results, canine mammary IMPCs show E-cadherin lost and, at times reveals nuclear positivity for the transcription factor ZEB2 that seems to exert transcriptional repression of the CDH1.A perda de E-caderina tem sido frequentemente associada à repressão transcricional mediada por fatores de transcrição, como o Zinc Finger E-Box Binding Homeobox-2 (ZEB2). Carcinomas micropapilares invasivos (IMPCs) da mama são neoplasias agressivas frequentemente relacionadas a metástases linfonodais e baixa sobrevida global. Na glândula mamária canina, os IMPCs acabam de ser relatados e, com base em sua semelhança comportamental com os IMPCs humanos, parecem ser um bom modelo espontâneo para essa entidade humana. Este estudo teve como objetivo avaliar a relação entre E-caderina e ZEB2 em um modelo canino espontâneo de carcinoma micropapilar invasivo da glândula mamária. A correlação entre a expressão gênica (ZEB2 e CDH1) e os achados clínico-patológicos também foi explorada. Dezenove casos de IMPC da glândula mamária canina foram obtidos, a expressão de proteína e mRNA foram investigadas por imuno-histoquímica e hibridização in situ de RNA, respectivamente. Para entender melhor a relação entre E-caderina e ZEB2, a imunofluorescência foi realizada em IMPCs caninos. Imuno-histoquimicamente, a maioria dos IMPCs mostrou 1+ (14/19, 73,7%) para E-caderina; e a positividade para ZEB2 foi diagnosticada em 47,4% dos IMPCs. Em relação à Hibridização In Situ de RNA (ISH), a maioria dos IMPCs apresentou 4+ e 0+ para E-caderina (CDH1) e ZEB2, respectivamente. Por imunofluorescência, o primeiro e o segundo grupo combinatório mais frequente foram E-caderina+ZEB2- e E-caderina+ZEB2+; células neoplásicas mostrando concomitantemente fraca expressão para E-caderina e positividade para ZEB2 foram freqüentemente observadas. Uma correlação negativa foi observada entre a E-caderina e a expressão do receptor de progesterona em IMPCs. Com base nesses resultados, os IMPCs mamários caninos apresentam perda de E-caderina e, por vezes, revela positividade nuclear para o fator de transcrição ZEB2 que parece exercer repressão transcricional do CDH1.CNPq - Conselho Nacional de Desenvolvimento Científico e TecnológicoFAPEMIG - Fundação de Amparo à Pesquisa do Estado de Minas GeraisCAPES - Coordenação de Aperfeiçoamento de Pessoal de Nível SuperiorengUniversidade Federal de Minas GeraisUFMGBrasilICB - DEPARTAMENTO DE BIOQUÍMICA E IMUNOLOGIAICB - DEPARTAMENTO DE PATOLOGIAPLoS ONEHomeobox 2 de ligação a E-box com dedos de zincoCaderinasNeoplasias da MamaZEB2E-cadherinmammary gland carcinomaThe investigation of transcriptional repression mediated by ZEB2 in canine invasive micropapillary carcinoma in mammary glandA investigação da repressão transcricional mediada por ZEB2 no carcinoma micropapilar invasivo canino na glândula mamáriainfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttps://journals.plos.org/plosone/article?id=10.1371/journal.pone.0209497Conrado de Oliveira GambaKarine Araújo DamascenoIzabel Cristina FerreiraMichele Angela RodriguesDawidson Assis GomesMariana Resende AlvesRafael Malagoli RochaAlessandra Estrela LimaEnio FerreiraGeovanni Dantas Cassaliapplication/pdfinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFMGinstname:Universidade Federal de Minas Gerais (UFMG)instacron:UFMGORIGINALThe investigation of transcriptional repression mediated by ZEB2 in canine invasive micropapillary carcinoma in mammary gland.pdfThe investigation of transcriptional repression mediated by ZEB2 in canine invasive micropapillary carcinoma in mammary gland.pdfapplication/pdf14051021https://repositorio.ufmg.br/bitstream/1843/56451/2/The%20investigation%20of%20transcriptional%20repression%20mediated%20by%20ZEB2%20in%20canine%20invasive%20micropapillary%20carcinoma%20in%20mammary%20gland.pdfd71c261724f701bc05a4fa92d0a4a691MD52LICENSELicense.txtLicense.txttext/plain; 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dc.title.pt_BR.fl_str_mv The investigation of transcriptional repression mediated by ZEB2 in canine invasive micropapillary carcinoma in mammary gland
dc.title.alternative.pt_BR.fl_str_mv A investigação da repressão transcricional mediada por ZEB2 no carcinoma micropapilar invasivo canino na glândula mamária
title The investigation of transcriptional repression mediated by ZEB2 in canine invasive micropapillary carcinoma in mammary gland
spellingShingle The investigation of transcriptional repression mediated by ZEB2 in canine invasive micropapillary carcinoma in mammary gland
Conrado de Oliveira Gamba
ZEB2
E-cadherin
mammary gland carcinoma
Homeobox 2 de ligação a E-box com dedos de zinco
Caderinas
Neoplasias da Mama
title_short The investigation of transcriptional repression mediated by ZEB2 in canine invasive micropapillary carcinoma in mammary gland
title_full The investigation of transcriptional repression mediated by ZEB2 in canine invasive micropapillary carcinoma in mammary gland
title_fullStr The investigation of transcriptional repression mediated by ZEB2 in canine invasive micropapillary carcinoma in mammary gland
title_full_unstemmed The investigation of transcriptional repression mediated by ZEB2 in canine invasive micropapillary carcinoma in mammary gland
title_sort The investigation of transcriptional repression mediated by ZEB2 in canine invasive micropapillary carcinoma in mammary gland
author Conrado de Oliveira Gamba
author_facet Conrado de Oliveira Gamba
Karine Araújo Damasceno
Izabel Cristina Ferreira
Michele Angela Rodrigues
Dawidson Assis Gomes
Mariana Resende Alves
Rafael Malagoli Rocha
Alessandra Estrela Lima
Enio Ferreira
Geovanni Dantas Cassali
author_role author
author2 Karine Araújo Damasceno
Izabel Cristina Ferreira
Michele Angela Rodrigues
Dawidson Assis Gomes
Mariana Resende Alves
Rafael Malagoli Rocha
Alessandra Estrela Lima
Enio Ferreira
Geovanni Dantas Cassali
author2_role author
author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Conrado de Oliveira Gamba
Karine Araújo Damasceno
Izabel Cristina Ferreira
Michele Angela Rodrigues
Dawidson Assis Gomes
Mariana Resende Alves
Rafael Malagoli Rocha
Alessandra Estrela Lima
Enio Ferreira
Geovanni Dantas Cassali
dc.subject.por.fl_str_mv ZEB2
E-cadherin
mammary gland carcinoma
topic ZEB2
E-cadherin
mammary gland carcinoma
Homeobox 2 de ligação a E-box com dedos de zinco
Caderinas
Neoplasias da Mama
dc.subject.other.pt_BR.fl_str_mv Homeobox 2 de ligação a E-box com dedos de zinco
Caderinas
Neoplasias da Mama
description The E-cadherin loss has frequently been associated with transcriptional repression mediated by transcription factors, such as the Zinc Finger E-Box Binding Homeobox-2 (ZEB2). Invasive micropapillary carcinomas (IMPCs) of the breast are aggressive neoplasms frequently related to lymph node metastasis and poor overall survival. In the canine mammary gland, IMPCs has just been reported and, based on its behavioral similarity with the human IMPCs, appears to be a good spontaneous model to this human entity. This study aimed to evaluate the relationship between E-cadherin and ZEB2 in a spontaneous canine model of invasive micropapillary carcinoma of the mammary gland. The correlation among gene expression (ZEB2 and CDH1) and clinicopathological findings was also explored. Nineteen cases of IMPC of the canine mammary gland were obtained, protein and mRNA expression were investigated through immunohistochemistry and RNA In Situ Hybridization, respectively. To better understand the relationship between E-cadherin and ZEB2, immunofluorescence was performed in canine IMPCs. Immunohistochemically, most of IMPCs showed 1+ (14/19, 73.7%) for E-cadherin; and positivity for ZEB2 was diagnosed in 47.4% of the IMPCs. Regarding the RNA In Situ Hybridization (ISH), most of IMPCs showed 4+ and 0+ for E-cadherin (CDH1) and ZEB2 respectively. Through immunofluorescence, the first and second more frequent combinatorial group were E-cadherin+ZEB2- and E-cadherin+ZEB2+; neoplastic cells showing concomitantly weak expression for E-cadherin and positivity for ZEB2 were frequently observed. A negative correlation was observed between E-cadherin and progesterone receptor expression in IMPCs. Based on these results, canine mammary IMPCs show E-cadherin lost and, at times reveals nuclear positivity for the transcription factor ZEB2 that seems to exert transcriptional repression of the CDH1.
publishDate 2019
dc.date.issued.fl_str_mv 2019
dc.date.accessioned.fl_str_mv 2023-07-17T19:01:37Z
dc.date.available.fl_str_mv 2023-07-17T19:01:37Z
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/1843/56451
dc.identifier.doi.pt_BR.fl_str_mv https://doi.org/10.1371/journal.pone.0209497
dc.identifier.issn.pt_BR.fl_str_mv 1932-6203
dc.identifier.orcid.pt_BR.fl_str_mv https://orcid.org/0000-0002-2035-8961
https://orcid.org/0000-0003-2087-1690
https://orcid.org/0000-0002-0233-7729
https://orcid.org/0000-0001-7714-991X
http://orcid.org/0000-0001-5904-4890
https://orcid.org/0000-0002-9879-7999
https://orcid.org/0000-0002-1835-0303
http://orcid.org/0000-0002-5650-6743
url https://doi.org/10.1371/journal.pone.0209497
http://hdl.handle.net/1843/56451
https://orcid.org/0000-0002-2035-8961
https://orcid.org/0000-0003-2087-1690
https://orcid.org/0000-0002-0233-7729
https://orcid.org/0000-0001-7714-991X
http://orcid.org/0000-0001-5904-4890
https://orcid.org/0000-0002-9879-7999
https://orcid.org/0000-0002-1835-0303
http://orcid.org/0000-0002-5650-6743
identifier_str_mv 1932-6203
dc.language.iso.fl_str_mv eng
language eng
dc.relation.ispartof.pt_BR.fl_str_mv PLoS ONE
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 Universidade Federal de Minas Gerais
dc.publisher.initials.fl_str_mv UFMG
dc.publisher.country.fl_str_mv Brasil
dc.publisher.department.fl_str_mv ICB - DEPARTAMENTO DE BIOQUÍMICA E IMUNOLOGIA
ICB - DEPARTAMENTO DE PATOLOGIA
publisher.none.fl_str_mv Universidade Federal de Minas Gerais
dc.source.none.fl_str_mv reponame:Repositório Institucional da UFMG
instname:Universidade Federal de Minas Gerais (UFMG)
instacron:UFMG
instname_str Universidade Federal de Minas Gerais (UFMG)
instacron_str UFMG
institution UFMG
reponame_str Repositório Institucional da UFMG
collection Repositório Institucional da UFMG
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