ETV4 plays a role on the primary events during the adenoma-adenocarcinoma progression in colorectal cancer
Autor(a) principal: | |
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Data de Publicação: | 2021 |
Outros Autores: | , , , , , , , , , , , , , , , , , , |
Tipo de documento: | Artigo |
Idioma: | por |
Título da fonte: | Repositório Institucional da FIOCRUZ (ARCA) |
Texto Completo: | https://www.arca.fiocruz.br/handle/icict/46942 |
Resumo: | Universidade de São Paulo. Faculdade de Medicina de Ribeirão Preto. Departamento de Genética. Ribeirão Preto, SP, Brasil. / Instituto Nacional de Ciências e Tecnologia em Células Tronco e Terapia Celular. Ribeirão Preto, SP, Brasil. / Centro de Terapia Celular. Ribeirão Preto, SP, Brasil. / Centro de Biologia de Sistemas Integrativos. Ribeirão Preto, SP, Brasil. / Instituto de Pesquisa Pelé Pequeno Príncipe. Curitiba, PR, Brasil. |
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Fonseca, Aline SimonetiRamão, AnelisaBürger, Matheus CarvalhoSouza, Jorge Estefano Santana deZanette, Dalila LucíolaMolfetta, Greice Andreotti deAraújo, Luiza Ferreira deBueno, Rafaela de Barros e LimaAguiar, Graziela MouraPlaça, Jessica RodriguesAlves, Cleidson de PáduaSantos, Anemari Ramos Dinarte dosVidal, Daniel OnofreSilva, Gyl Eanes BarrosPanepucci, Rodrigo AlexandrePeria, Fernanda MarisFeres, OmarRocha, José Joaquim Ribeiro daZago, Marco AntonioSilva Júnior, Wilson Araújo2021-04-27T19:35:13Z2021-04-27T19:35:13Z2021FONSECA, Aline Simoneti et al. ETV4 plays a role on the primary events during the adenoma-adenocarcinoma progression in colorectal cancer. BMC Cancer, v.21, n. 207, p. 1–14, 2021.1471-2407https://www.arca.fiocruz.br/handle/icict/4694210.1186/s12885-021-07857-xporBMCCâncer ColorretalETV4Colorectal NeoplasmsGenetic MarkersNeoplasias ColorrectalesMarcadores GenéticosAdénocarcinomeAdénomesTumeurs colorectalesMarqueurs génétiquesAdenocarcinomaAdenomaNeoplasias ColorretaisMarcadores GenéticosETV4 plays a role on the primary events during the adenoma-adenocarcinoma progression in colorectal cancerinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleUniversidade de São Paulo. Faculdade de Medicina de Ribeirão Preto. Departamento de Genética. Ribeirão Preto, SP, Brasil. / Instituto Nacional de Ciências e Tecnologia em Células Tronco e Terapia Celular. Ribeirão Preto, SP, Brasil. / Centro de Terapia Celular. Ribeirão Preto, SP, Brasil. / Centro de Biologia de Sistemas Integrativos. Ribeirão Preto, SP, Brasil. / Instituto de Pesquisa Pelé Pequeno Príncipe. Curitiba, PR, Brasil.Universidade de São Paulo. Faculdade de Medicina de Ribeirão Preto. Departamento de Genética. Ribeirão Preto, SP, Brasil. / Instituto Nacional de Ciências e Tecnologia em Células Tronco e Terapia Celular. Ribeirão Preto, SP, Brasil.Instituto Nacional de Ciências e Tecnologia em Células Tronco e Terapia Celular. Ribeirão Preto, SP, Brasil. / Centro de Terapia Celular. Ribeirão Preto, SP, Brasil.Instituto Nacional de Ciências e Tecnologia em Células Tronco e Terapia Celular. Ribeirão Preto, SP, Brasil. / Centro de Terapia Celular. Ribeirão Preto, SP, Brasil.Universidade de São Paulo. Faculdade de Medicina de Ribeirão Preto. Departamento de Genética. Ribeirão Preto, SP, Brasil. / Instituto Nacional de Ciências e Tecnologia em Células Tronco e Terapia Celular. Ribeirão Preto, SP, Brasil. / Centro de Terapia Celular. Ribeirão Preto, SP, Brasil. / Centro de Biologia de Sistemas Integrativos. Ribeirão Preto, SP, Brasil. / Fundação Oswaldo Cruz. Instituto Carlos Chagas. Laboratório de Ciências e Tecnologias Aplicadas em Saúde. Curitiba, PR, Brasil.Universidade de São Paulo. Faculdade de Medicina de Ribeirão Preto. Departamento de Genética. Ribeirão Preto, SP, Brasil. / Instituto Nacional de Ciências e Tecnologia em Células Tronco e Terapia Celular. Ribeirão Preto, SP, Brasil. / Centro de Terapia Celular. Ribeirão Preto, SP, Brasil. / Centro de Biologia de Sistemas Integrativos. Ribeirão Preto, SP, Brasil.Universidade de São Paulo. Faculdade de Medicina de Ribeirão Preto. Departamento de Genética. Ribeirão Preto, SP, Brasil. / Instituto Nacional de Ciências e Tecnologia em Células Tronco e Terapia Celular. Ribeirão Preto, SP, Brasil. / Centro de Terapia Celular. Ribeirão Preto, SP, Brasil. / Centro de Biologia de Sistemas Integrativos. Ribeirão Preto, SP, Brasil.Universidade de São Paulo. Faculdade de Medicina de Ribeirão Preto. Departamento de Genética. Ribeirão Preto, SP, Brasil. / Instituto Nacional de Ciências e Tecnologia em Células Tronco e Terapia Celular. Ribeirão Preto, SP, Brasil.Instituto Nacional de Ciências e Tecnologia em Células Tronco e Terapia Celular. Ribeirão Preto, SP, Brasil. / Centro de Terapia Celular. Ribeirão Preto, SP, Brasil.Instituto Nacional de Ciências e Tecnologia em Células Tronco e Terapia Celular. Ribeirão Preto, SP, Brasil. / Centro de Terapia Celular. Ribeirão Preto, SP, Brasil.Instituto Nacional de Ciências e Tecnologia em Células Tronco e Terapia Celular. Ribeirão Preto, SP, Brasil. / Centro de Terapia Celular. Ribeirão Preto, SP, Brasil.Instituto Nacional de Ciências e Tecnologia em Células Tronco e Terapia Celular. Ribeirão Preto, SP, Brasil. / Centro de Terapia Celular. Ribeirão Preto, SP, Brasil.Instituto Nacional de Ciências e Tecnologia em Células Tronco e Terapia Celular. Ribeirão Preto, SP, Brasil. / Centro de Terapia Celular. Ribeirão Preto, SP, Brasil.Hospital Universitário Presidente Dutra (HUUFMA). Laboratório de Imunofluorescência e Microscopia Eletrônica. São Luís, MA, Brasil.Instituto Nacional de Ciências e Tecnologia em Células Tronco e Terapia Celular. Ribeirão Preto, SP, Brasil. / Centro de Terapia Celular. Ribeirão Preto, SP, Brasil.Universidade de São Paulo. Faculdade de Medicina de Ribeirão Preto. Departamento de Clínica Médica. Ribeirão Preto, SP, Brasil.Universidade de São Paulo. Faculdade de Medicina de Ribeirão Preto. Departamento de Cirurgia e Anatomia. Ribeirão Preto, SP, Brasil.Universidade de São Paulo. Faculdade de Medicina de Ribeirão Preto. Departamento de Cirurgia e Anatomia. Ribeirão Preto, SP, Brasil.Instituto Nacional de Ciências e Tecnologia em Células Tronco e Terapia Celular. Ribeirão Preto, SP, Brasil. / Centro de Terapia Celular. Ribeirão Preto, SP, Brasil.Universidade de São Paulo. Faculdade de Medicina de Ribeirão Preto. Departamento de Genética. Ribeirão Preto, SP, Brasil. / Instituto Nacional de Ciências e Tecnologia em Células Tronco e Terapia Celular. Ribeirão Preto, SP, Brasil. / Centro de Terapia Celular. Ribeirão Preto, SP, Brasil. / Centro de Biologia de Sistemas Integrativos. Ribeirão Preto, SP, Brasil.Colorectal cancer (CRC) is one of the most common cancers worldwide; it is the fourth leading cause of death in the world and the third in Brazil. Mutations in the APC, DCC, KRAS and TP53 genes have been associated with the progression of sporadic CRC, occurring at defined pathological stages of the tumor progression and consequently modulating several genes in the corresponding signaling pathways. Therefore, the identification of gene signatures that occur at each stage during the CRC progression is critical and can present an impact on the diagnosis and prognosis of the patient. In this study, our main goal was to determine these signatures, by evaluating the gene expression of paired colorectal adenoma and adenocarcinoma samples to identify novel genetic markers in association to the adenoma-adenocarcinoma stage transition. As methods: ten paired adenoma and adenocarcinoma colorectal samples were subjected to microarray gene expression analysis. In addition, mutations in APC, KRAS and TP53 genes were investigated by DNA sequencing in paired samples of adenoma, adenocarcinoma, normal tissue, and peripheral blood from ten patients. In the results, gene expression analysis revealed a signature of 689 differentially expressed genes (DEG) (fold-change> 2, p< 0.05), between the adenoma and adenocarcinoma paired samples analyzed. Gene pathway analysis using the 689 DEG identified important cancer pathways such as remodeling of the extracellular matrix and epithelialmesenchymal transition. Among these DEG, the ETV4 stood out as one of the most expressed in the adenocarcinoma samples, further confirmed in the adenocarcinoma set of samples from the TCGA database. Subsequent in vitro siRNA assays against ETV4 resulted in the decrease of cell proliferation, colony formation and cell migration in the HT29 and SW480 colorectal cell lines. DNA sequencing analysis revealed KRAS and TP53 gene pathogenic mutations, exclusively in the adenocarcinomas samples. This way, our study identified a set of genes with high potential to be used as biomarkers in CRC, with a special emphasis on the ETV4 gene, which demonstrated involvement in proliferation and migration.info:eu-repo/semantics/openAccessreponame:Repositório Institucional da FIOCRUZ (ARCA)instname:Fundação Oswaldo Cruz (FIOCRUZ)instacron:FIOCRUZORIGINAL12885_2021_Article_7857ok.pdf12885_2021_Article_7857ok.pdfapplication/pdf1740374https://www.arca.fiocruz.br/bitstream/icict/46942/2/12885_2021_Article_7857ok.pdf61cf7554d39a666dca58fd17f8dd8befMD52LICENSElicense.txtlicense.txttext/plain; charset=utf-82991https://www.arca.fiocruz.br/bitstream/icict/46942/3/license.txt5a560609d32a3863062d77ff32785d58MD53TEXT12885_2021_Article_7857ok.pdf.txt12885_2021_Article_7857ok.pdf.txtExtracted texttext/plain60565https://www.arca.fiocruz.br/bitstream/icict/46942/4/12885_2021_Article_7857ok.pdf.txtb4a0023ae4309b92411d82b121092a35MD54icict/469422021-04-28 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dc.title.pt_BR.fl_str_mv |
ETV4 plays a role on the primary events during the adenoma-adenocarcinoma progression in colorectal cancer |
title |
ETV4 plays a role on the primary events during the adenoma-adenocarcinoma progression in colorectal cancer |
spellingShingle |
ETV4 plays a role on the primary events during the adenoma-adenocarcinoma progression in colorectal cancer Fonseca, Aline Simoneti Câncer Colorretal ETV4 Colorectal Neoplasms Genetic Markers Neoplasias Colorrectales Marcadores Genéticos Adénocarcinome Adénomes Tumeurs colorectales Marqueurs génétiques Adenocarcinoma Adenoma Neoplasias Colorretais Marcadores Genéticos |
title_short |
ETV4 plays a role on the primary events during the adenoma-adenocarcinoma progression in colorectal cancer |
title_full |
ETV4 plays a role on the primary events during the adenoma-adenocarcinoma progression in colorectal cancer |
title_fullStr |
ETV4 plays a role on the primary events during the adenoma-adenocarcinoma progression in colorectal cancer |
title_full_unstemmed |
ETV4 plays a role on the primary events during the adenoma-adenocarcinoma progression in colorectal cancer |
title_sort |
ETV4 plays a role on the primary events during the adenoma-adenocarcinoma progression in colorectal cancer |
author |
Fonseca, Aline Simoneti |
author_facet |
Fonseca, Aline Simoneti Ramão, Anelisa Bürger, Matheus Carvalho Souza, Jorge Estefano Santana de Zanette, Dalila Lucíola Molfetta, Greice Andreotti de Araújo, Luiza Ferreira de Bueno, Rafaela de Barros e Lima Aguiar, Graziela Moura Plaça, Jessica Rodrigues Alves, Cleidson de Pádua Santos, Anemari Ramos Dinarte dos Vidal, Daniel Onofre Silva, Gyl Eanes Barros Panepucci, Rodrigo Alexandre Peria, Fernanda Maris Feres, Omar Rocha, José Joaquim Ribeiro da Zago, Marco Antonio Silva Júnior, Wilson Araújo |
author_role |
author |
author2 |
Ramão, Anelisa Bürger, Matheus Carvalho Souza, Jorge Estefano Santana de Zanette, Dalila Lucíola Molfetta, Greice Andreotti de Araújo, Luiza Ferreira de Bueno, Rafaela de Barros e Lima Aguiar, Graziela Moura Plaça, Jessica Rodrigues Alves, Cleidson de Pádua Santos, Anemari Ramos Dinarte dos Vidal, Daniel Onofre Silva, Gyl Eanes Barros Panepucci, Rodrigo Alexandre Peria, Fernanda Maris Feres, Omar Rocha, José Joaquim Ribeiro da Zago, Marco Antonio Silva Júnior, Wilson Araújo |
author2_role |
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 |
Fonseca, Aline Simoneti Ramão, Anelisa Bürger, Matheus Carvalho Souza, Jorge Estefano Santana de Zanette, Dalila Lucíola Molfetta, Greice Andreotti de Araújo, Luiza Ferreira de Bueno, Rafaela de Barros e Lima Aguiar, Graziela Moura Plaça, Jessica Rodrigues Alves, Cleidson de Pádua Santos, Anemari Ramos Dinarte dos Vidal, Daniel Onofre Silva, Gyl Eanes Barros Panepucci, Rodrigo Alexandre Peria, Fernanda Maris Feres, Omar Rocha, José Joaquim Ribeiro da Zago, Marco Antonio Silva Júnior, Wilson Araújo |
dc.subject.other.pt_BR.fl_str_mv |
Câncer Colorretal ETV4 |
topic |
Câncer Colorretal ETV4 Colorectal Neoplasms Genetic Markers Neoplasias Colorrectales Marcadores Genéticos Adénocarcinome Adénomes Tumeurs colorectales Marqueurs génétiques Adenocarcinoma Adenoma Neoplasias Colorretais Marcadores Genéticos |
dc.subject.en.pt_BR.fl_str_mv |
Colorectal Neoplasms Genetic Markers |
dc.subject.es.pt_BR.fl_str_mv |
Neoplasias Colorrectales Marcadores Genéticos |
dc.subject.fr.pt_BR.fl_str_mv |
Adénocarcinome Adénomes Tumeurs colorectales Marqueurs génétiques |
dc.subject.decs.pt_BR.fl_str_mv |
Adenocarcinoma Adenoma Neoplasias Colorretais Marcadores Genéticos |
description |
Universidade de São Paulo. Faculdade de Medicina de Ribeirão Preto. Departamento de Genética. Ribeirão Preto, SP, Brasil. / Instituto Nacional de Ciências e Tecnologia em Células Tronco e Terapia Celular. Ribeirão Preto, SP, Brasil. / Centro de Terapia Celular. Ribeirão Preto, SP, Brasil. / Centro de Biologia de Sistemas Integrativos. Ribeirão Preto, SP, Brasil. / Instituto de Pesquisa Pelé Pequeno Príncipe. Curitiba, PR, Brasil. |
publishDate |
2021 |
dc.date.accessioned.fl_str_mv |
2021-04-27T19:35:13Z |
dc.date.available.fl_str_mv |
2021-04-27T19:35:13Z |
dc.date.issued.fl_str_mv |
2021 |
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.citation.fl_str_mv |
FONSECA, Aline Simoneti et al. ETV4 plays a role on the primary events during the adenoma-adenocarcinoma progression in colorectal cancer. BMC Cancer, v.21, n. 207, p. 1–14, 2021. |
dc.identifier.uri.fl_str_mv |
https://www.arca.fiocruz.br/handle/icict/46942 |
dc.identifier.issn.pt_BR.fl_str_mv |
1471-2407 |
dc.identifier.doi.none.fl_str_mv |
10.1186/s12885-021-07857-x |
identifier_str_mv |
FONSECA, Aline Simoneti et al. ETV4 plays a role on the primary events during the adenoma-adenocarcinoma progression in colorectal cancer. BMC Cancer, v.21, n. 207, p. 1–14, 2021. 1471-2407 10.1186/s12885-021-07857-x |
url |
https://www.arca.fiocruz.br/handle/icict/46942 |
dc.language.iso.fl_str_mv |
por |
language |
por |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
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openAccess |
dc.publisher.none.fl_str_mv |
BMC |
publisher.none.fl_str_mv |
BMC |
dc.source.none.fl_str_mv |
reponame:Repositório Institucional da FIOCRUZ (ARCA) instname:Fundação Oswaldo Cruz (FIOCRUZ) instacron:FIOCRUZ |
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Fundação Oswaldo Cruz (FIOCRUZ) |
instacron_str |
FIOCRUZ |
institution |
FIOCRUZ |
reponame_str |
Repositório Institucional da FIOCRUZ (ARCA) |
collection |
Repositório Institucional da FIOCRUZ (ARCA) |
bitstream.url.fl_str_mv |
https://www.arca.fiocruz.br/bitstream/icict/46942/2/12885_2021_Article_7857ok.pdf https://www.arca.fiocruz.br/bitstream/icict/46942/3/license.txt https://www.arca.fiocruz.br/bitstream/icict/46942/4/12885_2021_Article_7857ok.pdf.txt |
bitstream.checksum.fl_str_mv |
61cf7554d39a666dca58fd17f8dd8bef 5a560609d32a3863062d77ff32785d58 b4a0023ae4309b92411d82b121092a35 |
bitstream.checksumAlgorithm.fl_str_mv |
MD5 MD5 MD5 |
repository.name.fl_str_mv |
Repositório Institucional da FIOCRUZ (ARCA) - Fundação Oswaldo Cruz (FIOCRUZ) |
repository.mail.fl_str_mv |
repositorio.arca@fiocruz.br |
_version_ |
1798325088821444608 |