PLAGL1 gene function during hepatoma cells proliferation
- Autores
- Vega Benedetti, Ana Florencia; Saucedo, Cinthia Natalia; Zavattari, Patrizia; Vanni, Roberta; Royo, Felix; LLavero, Freancisco; Zugaza, José L.; Parada, Luis Antonio
- Año de publicación
- 2018
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- Hepatocellular carcinoma develops as a multistep process, in which cell cycle deregulation is a central feature, resulting in unscheduled proliferation. The PLAGL1 gene encodes a homonym zinc finger protein that is involved in cell-proliferation control. We determined the genomic profile and the transcription and expression level of PLAGL1, simultaneously with that of its molecular partners p53, PPARγ and p21, in cell-lines derived from patients with liver cancer, during in vitro cell growth. Our investigations revealed that genomic and epigenetic changes of PLAGL1 are also present in hepatoma cell-lines. Transcription of PLAGL1 in tumor cells is significantly lower than in normal fibroblasts, but no significant differences in terms of protein expression were detected between these two cell-types, indicating that there is not a direct relationship between the gene transcriptional activity and protein expression. RT-PCR analyses on normal fibroblasts, used as control, also showed that PLAGL1 and p53 genes transcription occurs as an apparent orchestrated process during normal cells proliferation, which gets disturbed in cancer cells. Furthermore, abnormal trafficking of the PLAGL1 protein may occur in hepatocarcinogenesis.
Fil: Vega Benedetti, Ana Florencia. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Salta. Instituto de Patología Experimental. Universidad Nacional de Salta. Facultad de Ciencias de la Salud. Instituto de Patología Experimental; Argentina
Fil: Saucedo, Cinthia Natalia. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Salta. Instituto de Patología Experimental. Universidad Nacional de Salta. Facultad de Ciencias de la Salud. Instituto de Patología Experimental; Argentina
Fil: Zavattari, Patrizia. University of Cagliari; Italia
Fil: Vanni, Roberta. University of Cagliari; Italia
Fil: Royo, Felix. CIC BioGUNE CIBERehd; España
Fil: LLavero, Freancisco. Universidad del País Vasco; España. IKERBASQUE; España
Fil: Zugaza, José L.. Universidad del País Vasco; España. IKERBASQUE; España
Fil: Parada, Luis Antonio. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Salta. Instituto de Patología Experimental. Universidad Nacional de Salta. Facultad de Ciencias de la Salud. Instituto de Patología Experimental; Argentina - Materia
-
CELL PROLIFERATION
CHROMOSOME
HEPATOCELLULAR CARCINOMA
METHYLATION
PLAGL1 - 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:11336/86657
Ver los metadatos del registro completo
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oai:ri.conicet.gov.ar:11336/86657 |
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CONICET Digital (CONICET) |
spelling |
PLAGL1 gene function during hepatoma cells proliferationVega Benedetti, Ana FlorenciaSaucedo, Cinthia NataliaZavattari, PatriziaVanni, RobertaRoyo, FelixLLavero, FreanciscoZugaza, José L.Parada, Luis AntonioCELL PROLIFERATIONCHROMOSOMEHEPATOCELLULAR CARCINOMAMETHYLATIONPLAGL1https://purl.org/becyt/ford/3.5https://purl.org/becyt/ford/3Hepatocellular carcinoma develops as a multistep process, in which cell cycle deregulation is a central feature, resulting in unscheduled proliferation. The PLAGL1 gene encodes a homonym zinc finger protein that is involved in cell-proliferation control. We determined the genomic profile and the transcription and expression level of PLAGL1, simultaneously with that of its molecular partners p53, PPARγ and p21, in cell-lines derived from patients with liver cancer, during in vitro cell growth. Our investigations revealed that genomic and epigenetic changes of PLAGL1 are also present in hepatoma cell-lines. Transcription of PLAGL1 in tumor cells is significantly lower than in normal fibroblasts, but no significant differences in terms of protein expression were detected between these two cell-types, indicating that there is not a direct relationship between the gene transcriptional activity and protein expression. RT-PCR analyses on normal fibroblasts, used as control, also showed that PLAGL1 and p53 genes transcription occurs as an apparent orchestrated process during normal cells proliferation, which gets disturbed in cancer cells. Furthermore, abnormal trafficking of the PLAGL1 protein may occur in hepatocarcinogenesis.Fil: Vega Benedetti, Ana Florencia. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Salta. Instituto de Patología Experimental. Universidad Nacional de Salta. Facultad de Ciencias de la Salud. Instituto de Patología Experimental; ArgentinaFil: Saucedo, Cinthia Natalia. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Salta. Instituto de Patología Experimental. Universidad Nacional de Salta. Facultad de Ciencias de la Salud. Instituto de Patología Experimental; ArgentinaFil: Zavattari, Patrizia. University of Cagliari; ItaliaFil: Vanni, Roberta. University of Cagliari; ItaliaFil: Royo, Felix. CIC BioGUNE CIBERehd; EspañaFil: LLavero, Freancisco. Universidad del País Vasco; España. IKERBASQUE; EspañaFil: Zugaza, José L.. Universidad del País Vasco; España. IKERBASQUE; EspañaFil: Parada, Luis Antonio. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Salta. Instituto de Patología Experimental. Universidad Nacional de Salta. Facultad de Ciencias de la Salud. Instituto de Patología Experimental; ArgentinaImpact Journals LLC2018-08-28info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/86657Vega Benedetti, Ana Florencia; Saucedo, Cinthia Natalia; Zavattari, Patrizia; Vanni, Roberta; Royo, Felix; et al.; PLAGL1 gene function during hepatoma cells proliferation; Impact Journals LLC; Oncotarget; 9; 67; 28-8-2018; 32775-327941949-2553CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/doi/10.18632/oncotarget.25996info:eu-repo/semantics/altIdentifier/url/http://www.oncotarget.com/index.php?journal=oncotarget&page=article&op=view&path[]=25996&path[]=81113info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-29T10:20:57Zoai:ri.conicet.gov.ar:11336/86657instacron: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:34982025-09-29 10:20:57.653CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
dc.title.none.fl_str_mv |
PLAGL1 gene function during hepatoma cells proliferation |
title |
PLAGL1 gene function during hepatoma cells proliferation |
spellingShingle |
PLAGL1 gene function during hepatoma cells proliferation Vega Benedetti, Ana Florencia CELL PROLIFERATION CHROMOSOME HEPATOCELLULAR CARCINOMA METHYLATION PLAGL1 |
title_short |
PLAGL1 gene function during hepatoma cells proliferation |
title_full |
PLAGL1 gene function during hepatoma cells proliferation |
title_fullStr |
PLAGL1 gene function during hepatoma cells proliferation |
title_full_unstemmed |
PLAGL1 gene function during hepatoma cells proliferation |
title_sort |
PLAGL1 gene function during hepatoma cells proliferation |
dc.creator.none.fl_str_mv |
Vega Benedetti, Ana Florencia Saucedo, Cinthia Natalia Zavattari, Patrizia Vanni, Roberta Royo, Felix LLavero, Freancisco Zugaza, José L. Parada, Luis Antonio |
author |
Vega Benedetti, Ana Florencia |
author_facet |
Vega Benedetti, Ana Florencia Saucedo, Cinthia Natalia Zavattari, Patrizia Vanni, Roberta Royo, Felix LLavero, Freancisco Zugaza, José L. Parada, Luis Antonio |
author_role |
author |
author2 |
Saucedo, Cinthia Natalia Zavattari, Patrizia Vanni, Roberta Royo, Felix LLavero, Freancisco Zugaza, José L. Parada, Luis Antonio |
author2_role |
author author author author author author author |
dc.subject.none.fl_str_mv |
CELL PROLIFERATION CHROMOSOME HEPATOCELLULAR CARCINOMA METHYLATION PLAGL1 |
topic |
CELL PROLIFERATION CHROMOSOME HEPATOCELLULAR CARCINOMA METHYLATION PLAGL1 |
purl_subject.fl_str_mv |
https://purl.org/becyt/ford/3.5 https://purl.org/becyt/ford/3 |
dc.description.none.fl_txt_mv |
Hepatocellular carcinoma develops as a multistep process, in which cell cycle deregulation is a central feature, resulting in unscheduled proliferation. The PLAGL1 gene encodes a homonym zinc finger protein that is involved in cell-proliferation control. We determined the genomic profile and the transcription and expression level of PLAGL1, simultaneously with that of its molecular partners p53, PPARγ and p21, in cell-lines derived from patients with liver cancer, during in vitro cell growth. Our investigations revealed that genomic and epigenetic changes of PLAGL1 are also present in hepatoma cell-lines. Transcription of PLAGL1 in tumor cells is significantly lower than in normal fibroblasts, but no significant differences in terms of protein expression were detected between these two cell-types, indicating that there is not a direct relationship between the gene transcriptional activity and protein expression. RT-PCR analyses on normal fibroblasts, used as control, also showed that PLAGL1 and p53 genes transcription occurs as an apparent orchestrated process during normal cells proliferation, which gets disturbed in cancer cells. Furthermore, abnormal trafficking of the PLAGL1 protein may occur in hepatocarcinogenesis. Fil: Vega Benedetti, Ana Florencia. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Salta. Instituto de Patología Experimental. Universidad Nacional de Salta. Facultad de Ciencias de la Salud. Instituto de Patología Experimental; Argentina Fil: Saucedo, Cinthia Natalia. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Salta. Instituto de Patología Experimental. Universidad Nacional de Salta. Facultad de Ciencias de la Salud. Instituto de Patología Experimental; Argentina Fil: Zavattari, Patrizia. University of Cagliari; Italia Fil: Vanni, Roberta. University of Cagliari; Italia Fil: Royo, Felix. CIC BioGUNE CIBERehd; España Fil: LLavero, Freancisco. Universidad del País Vasco; España. IKERBASQUE; España Fil: Zugaza, José L.. Universidad del País Vasco; España. IKERBASQUE; España Fil: Parada, Luis Antonio. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Salta. Instituto de Patología Experimental. Universidad Nacional de Salta. Facultad de Ciencias de la Salud. Instituto de Patología Experimental; Argentina |
description |
Hepatocellular carcinoma develops as a multistep process, in which cell cycle deregulation is a central feature, resulting in unscheduled proliferation. The PLAGL1 gene encodes a homonym zinc finger protein that is involved in cell-proliferation control. We determined the genomic profile and the transcription and expression level of PLAGL1, simultaneously with that of its molecular partners p53, PPARγ and p21, in cell-lines derived from patients with liver cancer, during in vitro cell growth. Our investigations revealed that genomic and epigenetic changes of PLAGL1 are also present in hepatoma cell-lines. Transcription of PLAGL1 in tumor cells is significantly lower than in normal fibroblasts, but no significant differences in terms of protein expression were detected between these two cell-types, indicating that there is not a direct relationship between the gene transcriptional activity and protein expression. RT-PCR analyses on normal fibroblasts, used as control, also showed that PLAGL1 and p53 genes transcription occurs as an apparent orchestrated process during normal cells proliferation, which gets disturbed in cancer cells. Furthermore, abnormal trafficking of the PLAGL1 protein may occur in hepatocarcinogenesis. |
publishDate |
2018 |
dc.date.none.fl_str_mv |
2018-08-28 |
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/11336/86657 Vega Benedetti, Ana Florencia; Saucedo, Cinthia Natalia; Zavattari, Patrizia; Vanni, Roberta; Royo, Felix; et al.; PLAGL1 gene function during hepatoma cells proliferation; Impact Journals LLC; Oncotarget; 9; 67; 28-8-2018; 32775-32794 1949-2553 CONICET Digital CONICET |
url |
http://hdl.handle.net/11336/86657 |
identifier_str_mv |
Vega Benedetti, Ana Florencia; Saucedo, Cinthia Natalia; Zavattari, Patrizia; Vanni, Roberta; Royo, Felix; et al.; PLAGL1 gene function during hepatoma cells proliferation; Impact Journals LLC; Oncotarget; 9; 67; 28-8-2018; 32775-32794 1949-2553 CONICET Digital CONICET |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
info:eu-repo/semantics/altIdentifier/doi/10.18632/oncotarget.25996 info:eu-repo/semantics/altIdentifier/url/http://www.oncotarget.com/index.php?journal=oncotarget&page=article&op=view&path[]=25996&path[]=81113 |
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 |
dc.publisher.none.fl_str_mv |
Impact Journals LLC |
publisher.none.fl_str_mv |
Impact Journals LLC |
dc.source.none.fl_str_mv |
reponame:CONICET Digital (CONICET) instname:Consejo Nacional de Investigaciones Científicas y Técnicas |
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CONICET Digital (CONICET) |
collection |
CONICET Digital (CONICET) |
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Consejo Nacional de Investigaciones Científicas y Técnicas |
repository.name.fl_str_mv |
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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13.070432 |