ETV5 transcription factor is upregulated in ovarian cancer and contributes to ovarian tumor progression and dissemination
- Autores
- Llaurado, Marta; Abal, Miguel; Castellví, Josep; Cabrera, Silvia; Gil Moreno, Antonio; Pérez Benavente, Asumpció; Colás, Eva; Doll, Andreas; Dolcet, Xavier; Matias Guiu, Xavier; Vazquez, Monica Hebe; Reventós, Jaume; Ruiz, Anna
- Año de publicación
- 2011
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- Epithelial ovarian cancer is the most lethal gynecological malignancy and the fifth leading cause of cancer deaths in women in the Western world. ETS transcription factors are known to act as positive or negative regulators of the expression of genes that are involved in various biological processes, including those that control cellular proliferation, differentiation, apoptosis, tissue remodeling, angiogenesis and transformation. ETV5 belongs to the PEA3 subfamily. PEA3 subfamily members are able to activate the transcription of proteases, matrix metalloproteinases and tissue inhibitor of metalloproteases, which is central to both tumor invasion and angiogenesis. Here, we examined the role of the ETV5 transcription factor in epithelial ovarian cancer and we found ETV5 was upregulated in ovarian tumor samples compared to ovarian tissue controls. The in vitro inhibition of ETV5 decreased cell proliferation in serum-deprived conditions, induced EMT and cell migration and decreased cell adhesion to extracellular matrix components. ETV5 inhibition also decreased cell–cell adhesion and induced apoptosis in anchorage-independent conditions. Accordingly, upregulation of ETV5 induced the expression of cell adhesion molecules and enhanced cell survival in a spheroid model. Our findings suggest that the overexpression of ETV5 detected in ovarian cancer cells may contribute to ovarian tumor progression through the ability of ETV5 to enhance proliferation of ovarian cancer cells. In addition, upregulation of ETV5 would play a role in ovarian cancer cell dissemination and metastasis into the peritoneal cavity by protecting ovarian cancer cells from apoptosis and by increasing the adhesion of ovarian cancer cells to the peritoneal wall through the regulation of cell adhesion molecules.
Fil: Llaurado, Marta. Universidad Autonoma de Barcelona. Hospital Vall D; España
Fil: Abal, Miguel. Universidad Autonoma de Barcelona. Hospital Vall D; España
Fil: Castellví, Josep. Universidad Autónoma de Barcelona. Hospital Vall D; España
Fil: Cabrera, Silvia. Universidad Autonoma de Barcelona. Hospital Vall D; España
Fil: Gil Moreno, Antonio. Universitat Autònoma de Barcelona; España. Universidad Autónoma de Barcelona. Hospital Vall D; España
Fil: Pérez Benavente, Asumpció. Universidad Autónoma de Barcelona. Hospital Vall D; España
Fil: Colás, Eva. Universidad Autonoma de Barcelona. Hospital Vall D; España
Fil: Doll, Andreas. Universidad Autonoma de Barcelona. Hospital Vall D; España
Fil: Dolcet, Xavier. Universidad de Lleida. Instituto de Recerca Biomédica.; España
Fil: Matias Guiu, Xavier. Universidad de Lleida. Instituto de Recerca Biomédica.; España
Fil: Vazquez, Monica Hebe. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Biología y Medicina Experimental. Fundación de Instituto de Biología y Medicina Experimental. Instituto de Biología y Medicina Experimental; Argentina
Fil: Reventós, Jaume. Universidad Autonoma de Barcelona. Hospital Vall D; España. Universitat Autònoma de Barcelona; España
Fil: Ruiz, Anna. Universidad Autonoma de Barcelona. Hospital Vall D; España - Materia
-
Ovarian Cancer
Etv5
Epithelial Cadherin
Emt - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
- Repositorio
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/22269
Ver los metadatos del registro completo
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ETV5 transcription factor is upregulated in ovarian cancer and contributes to ovarian tumor progression and disseminationLlaurado, MartaAbal, MiguelCastellví, JosepCabrera, SilviaGil Moreno, AntonioPérez Benavente, AsumpcióColás, EvaDoll, AndreasDolcet, XavierMatias Guiu, XavierVazquez, Monica HebeReventós, JaumeRuiz, AnnaOvarian CancerEtv5Epithelial CadherinEmthttps://purl.org/becyt/ford/3.1https://purl.org/becyt/ford/3https://purl.org/becyt/ford/3.2https://purl.org/becyt/ford/3Epithelial ovarian cancer is the most lethal gynecological malignancy and the fifth leading cause of cancer deaths in women in the Western world. ETS transcription factors are known to act as positive or negative regulators of the expression of genes that are involved in various biological processes, including those that control cellular proliferation, differentiation, apoptosis, tissue remodeling, angiogenesis and transformation. ETV5 belongs to the PEA3 subfamily. PEA3 subfamily members are able to activate the transcription of proteases, matrix metalloproteinases and tissue inhibitor of metalloproteases, which is central to both tumor invasion and angiogenesis. Here, we examined the role of the ETV5 transcription factor in epithelial ovarian cancer and we found ETV5 was upregulated in ovarian tumor samples compared to ovarian tissue controls. The in vitro inhibition of ETV5 decreased cell proliferation in serum-deprived conditions, induced EMT and cell migration and decreased cell adhesion to extracellular matrix components. ETV5 inhibition also decreased cell–cell adhesion and induced apoptosis in anchorage-independent conditions. Accordingly, upregulation of ETV5 induced the expression of cell adhesion molecules and enhanced cell survival in a spheroid model. Our findings suggest that the overexpression of ETV5 detected in ovarian cancer cells may contribute to ovarian tumor progression through the ability of ETV5 to enhance proliferation of ovarian cancer cells. In addition, upregulation of ETV5 would play a role in ovarian cancer cell dissemination and metastasis into the peritoneal cavity by protecting ovarian cancer cells from apoptosis and by increasing the adhesion of ovarian cancer cells to the peritoneal wall through the regulation of cell adhesion molecules.Fil: Llaurado, Marta. Universidad Autonoma de Barcelona. Hospital Vall D; EspañaFil: Abal, Miguel. Universidad Autonoma de Barcelona. Hospital Vall D; EspañaFil: Castellví, Josep. Universidad Autónoma de Barcelona. Hospital Vall D; EspañaFil: Cabrera, Silvia. Universidad Autonoma de Barcelona. Hospital Vall D; EspañaFil: Gil Moreno, Antonio. Universitat Autònoma de Barcelona; España. Universidad Autónoma de Barcelona. Hospital Vall D; EspañaFil: Pérez Benavente, Asumpció. Universidad Autónoma de Barcelona. Hospital Vall D; EspañaFil: Colás, Eva. Universidad Autonoma de Barcelona. Hospital Vall D; EspañaFil: Doll, Andreas. Universidad Autonoma de Barcelona. Hospital Vall D; EspañaFil: Dolcet, Xavier. Universidad de Lleida. Instituto de Recerca Biomédica.; EspañaFil: Matias Guiu, Xavier. Universidad de Lleida. Instituto de Recerca Biomédica.; EspañaFil: Vazquez, Monica Hebe. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Biología y Medicina Experimental. Fundación de Instituto de Biología y Medicina Experimental. Instituto de Biología y Medicina Experimental; ArgentinaFil: Reventós, Jaume. Universidad Autonoma de Barcelona. Hospital Vall D; España. Universitat Autònoma de Barcelona; EspañaFil: Ruiz, Anna. Universidad Autonoma de Barcelona. Hospital Vall D; EspañaWiley2011-08info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/22269Llaurado, Marta; Abal, Miguel; Castellví, Josep; Cabrera, Silvia; Gil Moreno, Antonio; et al.; ETV5 transcription factor is upregulated in ovarian cancer and contributes to ovarian tumor progression and dissemination; Wiley; International Journal Of Cancer. Journal International Du Cancer.; 130; 7; 8-2011; 1532-15430020-71361097-0215CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/http://onlinelibrary.wiley.com/doi/10.1002/ijc.26148/abstractinfo:eu-repo/semantics/altIdentifier/doi/10.1002/ijc.26148info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-03T09:58:53Zoai:ri.conicet.gov.ar:11336/22269instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-09-03 09:58:53.557CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
dc.title.none.fl_str_mv |
ETV5 transcription factor is upregulated in ovarian cancer and contributes to ovarian tumor progression and dissemination |
title |
ETV5 transcription factor is upregulated in ovarian cancer and contributes to ovarian tumor progression and dissemination |
spellingShingle |
ETV5 transcription factor is upregulated in ovarian cancer and contributes to ovarian tumor progression and dissemination Llaurado, Marta Ovarian Cancer Etv5 Epithelial Cadherin Emt |
title_short |
ETV5 transcription factor is upregulated in ovarian cancer and contributes to ovarian tumor progression and dissemination |
title_full |
ETV5 transcription factor is upregulated in ovarian cancer and contributes to ovarian tumor progression and dissemination |
title_fullStr |
ETV5 transcription factor is upregulated in ovarian cancer and contributes to ovarian tumor progression and dissemination |
title_full_unstemmed |
ETV5 transcription factor is upregulated in ovarian cancer and contributes to ovarian tumor progression and dissemination |
title_sort |
ETV5 transcription factor is upregulated in ovarian cancer and contributes to ovarian tumor progression and dissemination |
dc.creator.none.fl_str_mv |
Llaurado, Marta Abal, Miguel Castellví, Josep Cabrera, Silvia Gil Moreno, Antonio Pérez Benavente, Asumpció Colás, Eva Doll, Andreas Dolcet, Xavier Matias Guiu, Xavier Vazquez, Monica Hebe Reventós, Jaume Ruiz, Anna |
author |
Llaurado, Marta |
author_facet |
Llaurado, Marta Abal, Miguel Castellví, Josep Cabrera, Silvia Gil Moreno, Antonio Pérez Benavente, Asumpció Colás, Eva Doll, Andreas Dolcet, Xavier Matias Guiu, Xavier Vazquez, Monica Hebe Reventós, Jaume Ruiz, Anna |
author_role |
author |
author2 |
Abal, Miguel Castellví, Josep Cabrera, Silvia Gil Moreno, Antonio Pérez Benavente, Asumpció Colás, Eva Doll, Andreas Dolcet, Xavier Matias Guiu, Xavier Vazquez, Monica Hebe Reventós, Jaume Ruiz, Anna |
author2_role |
author author author author author author author author author author author author |
dc.subject.none.fl_str_mv |
Ovarian Cancer Etv5 Epithelial Cadherin Emt |
topic |
Ovarian Cancer Etv5 Epithelial Cadherin Emt |
purl_subject.fl_str_mv |
https://purl.org/becyt/ford/3.1 https://purl.org/becyt/ford/3 https://purl.org/becyt/ford/3.2 https://purl.org/becyt/ford/3 |
dc.description.none.fl_txt_mv |
Epithelial ovarian cancer is the most lethal gynecological malignancy and the fifth leading cause of cancer deaths in women in the Western world. ETS transcription factors are known to act as positive or negative regulators of the expression of genes that are involved in various biological processes, including those that control cellular proliferation, differentiation, apoptosis, tissue remodeling, angiogenesis and transformation. ETV5 belongs to the PEA3 subfamily. PEA3 subfamily members are able to activate the transcription of proteases, matrix metalloproteinases and tissue inhibitor of metalloproteases, which is central to both tumor invasion and angiogenesis. Here, we examined the role of the ETV5 transcription factor in epithelial ovarian cancer and we found ETV5 was upregulated in ovarian tumor samples compared to ovarian tissue controls. The in vitro inhibition of ETV5 decreased cell proliferation in serum-deprived conditions, induced EMT and cell migration and decreased cell adhesion to extracellular matrix components. ETV5 inhibition also decreased cell–cell adhesion and induced apoptosis in anchorage-independent conditions. Accordingly, upregulation of ETV5 induced the expression of cell adhesion molecules and enhanced cell survival in a spheroid model. Our findings suggest that the overexpression of ETV5 detected in ovarian cancer cells may contribute to ovarian tumor progression through the ability of ETV5 to enhance proliferation of ovarian cancer cells. In addition, upregulation of ETV5 would play a role in ovarian cancer cell dissemination and metastasis into the peritoneal cavity by protecting ovarian cancer cells from apoptosis and by increasing the adhesion of ovarian cancer cells to the peritoneal wall through the regulation of cell adhesion molecules. Fil: Llaurado, Marta. Universidad Autonoma de Barcelona. Hospital Vall D; España Fil: Abal, Miguel. Universidad Autonoma de Barcelona. Hospital Vall D; España Fil: Castellví, Josep. Universidad Autónoma de Barcelona. Hospital Vall D; España Fil: Cabrera, Silvia. Universidad Autonoma de Barcelona. Hospital Vall D; España Fil: Gil Moreno, Antonio. Universitat Autònoma de Barcelona; España. Universidad Autónoma de Barcelona. Hospital Vall D; España Fil: Pérez Benavente, Asumpció. Universidad Autónoma de Barcelona. Hospital Vall D; España Fil: Colás, Eva. Universidad Autonoma de Barcelona. Hospital Vall D; España Fil: Doll, Andreas. Universidad Autonoma de Barcelona. Hospital Vall D; España Fil: Dolcet, Xavier. Universidad de Lleida. Instituto de Recerca Biomédica.; España Fil: Matias Guiu, Xavier. Universidad de Lleida. Instituto de Recerca Biomédica.; España Fil: Vazquez, Monica Hebe. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Biología y Medicina Experimental. Fundación de Instituto de Biología y Medicina Experimental. Instituto de Biología y Medicina Experimental; Argentina Fil: Reventós, Jaume. Universidad Autonoma de Barcelona. Hospital Vall D; España. Universitat Autònoma de Barcelona; España Fil: Ruiz, Anna. Universidad Autonoma de Barcelona. Hospital Vall D; España |
description |
Epithelial ovarian cancer is the most lethal gynecological malignancy and the fifth leading cause of cancer deaths in women in the Western world. ETS transcription factors are known to act as positive or negative regulators of the expression of genes that are involved in various biological processes, including those that control cellular proliferation, differentiation, apoptosis, tissue remodeling, angiogenesis and transformation. ETV5 belongs to the PEA3 subfamily. PEA3 subfamily members are able to activate the transcription of proteases, matrix metalloproteinases and tissue inhibitor of metalloproteases, which is central to both tumor invasion and angiogenesis. Here, we examined the role of the ETV5 transcription factor in epithelial ovarian cancer and we found ETV5 was upregulated in ovarian tumor samples compared to ovarian tissue controls. The in vitro inhibition of ETV5 decreased cell proliferation in serum-deprived conditions, induced EMT and cell migration and decreased cell adhesion to extracellular matrix components. ETV5 inhibition also decreased cell–cell adhesion and induced apoptosis in anchorage-independent conditions. Accordingly, upregulation of ETV5 induced the expression of cell adhesion molecules and enhanced cell survival in a spheroid model. Our findings suggest that the overexpression of ETV5 detected in ovarian cancer cells may contribute to ovarian tumor progression through the ability of ETV5 to enhance proliferation of ovarian cancer cells. In addition, upregulation of ETV5 would play a role in ovarian cancer cell dissemination and metastasis into the peritoneal cavity by protecting ovarian cancer cells from apoptosis and by increasing the adhesion of ovarian cancer cells to the peritoneal wall through the regulation of cell adhesion molecules. |
publishDate |
2011 |
dc.date.none.fl_str_mv |
2011-08 |
dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion http://purl.org/coar/resource_type/c_6501 info:ar-repo/semantics/articulo |
format |
article |
status_str |
publishedVersion |
dc.identifier.none.fl_str_mv |
http://hdl.handle.net/11336/22269 Llaurado, Marta; Abal, Miguel; Castellví, Josep; Cabrera, Silvia; Gil Moreno, Antonio; et al.; ETV5 transcription factor is upregulated in ovarian cancer and contributes to ovarian tumor progression and dissemination; Wiley; International Journal Of Cancer. Journal International Du Cancer.; 130; 7; 8-2011; 1532-1543 0020-7136 1097-0215 CONICET Digital CONICET |
url |
http://hdl.handle.net/11336/22269 |
identifier_str_mv |
Llaurado, Marta; Abal, Miguel; Castellví, Josep; Cabrera, Silvia; Gil Moreno, Antonio; et al.; ETV5 transcription factor is upregulated in ovarian cancer and contributes to ovarian tumor progression and dissemination; Wiley; International Journal Of Cancer. Journal International Du Cancer.; 130; 7; 8-2011; 1532-1543 0020-7136 1097-0215 CONICET Digital CONICET |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
info:eu-repo/semantics/altIdentifier/url/http://onlinelibrary.wiley.com/doi/10.1002/ijc.26148/abstract info:eu-repo/semantics/altIdentifier/doi/10.1002/ijc.26148 |
dc.rights.none.fl_str_mv |
info:eu-repo/semantics/openAccess https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
eu_rights_str_mv |
openAccess |
rights_invalid_str_mv |
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
dc.format.none.fl_str_mv |
application/pdf application/pdf application/pdf |
dc.publisher.none.fl_str_mv |
Wiley |
publisher.none.fl_str_mv |
Wiley |
dc.source.none.fl_str_mv |
reponame:CONICET Digital (CONICET) instname:Consejo Nacional de Investigaciones Científicas y Técnicas |
reponame_str |
CONICET Digital (CONICET) |
collection |
CONICET Digital (CONICET) |
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Consejo Nacional de Investigaciones Científicas y Técnicas |
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CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas |
repository.mail.fl_str_mv |
dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar |
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1842269548531679232 |
score |
13.13397 |