Do GnRH analogues directly affect human endometrial epithelial cell gene expression?

Autores
Zhang, Xiaomei; Bocca, Silvina; Franchi, Nilda Anahi; Anderson, Sandra; Kaur, Mandeep; Bajic, Vladimir B.; Oehninger, Sergio
Año de publicación
2010
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
We examined whether Gonadotrophin-releasing hormone (GnRH) analogues [leuprolide acetate (LA) and ganirelix acetate (GA)] modulate gene expression in Ishikawa cells used as surrogate for human endometrial epithelial cells in vitro. The specific aims were: (i) to study the modulatory effect of GnRH analogues by RT –PCR [in the absence and presence of E2 and P4, and cyclic adenosine monophosphate (cAMP)] on mRNA expression of genes modulated during the window of implantation in GnRH analogues/rFSH-treated assisted reproductive technology cycles including OPTINEURIN (OPTN), CHROMATIN MODIFYING PROTEIN (CHMP1A), PROSAPOSIN (PSAP), IGFBP-5 and SORTING NEXIN 7 (SNX7), and (ii) to analyze the 5′ -flanking regions of such genes for the presence of putative steroid-response elements [estrogen-response elements (EREs) and P4-response element (PREs)]. Ishikawa cells were cytokeratin+/vimentin2 and expressed ERa, ERb, PR and GnRH-R proteins. At 6 and 24 h, neither LA nor GA alone had an effect on gene expression. GnRH analogues alone or following E2 and/or P4 co-incubation for 24 h also had no effect on gene expression, but P4 significantly increased expression of CHMP1A. E2 + P4 treatment for 4 days, alone or followed by GA, had no effect, but E2 + P4 treatment followed by LA significantly decreased IGFBP-5 expression. The addition of 8-Br cAMP did not modify gene expression, with the exception of IGFBP-5 that was significantly increased. The GnRH analogues did not modify intracellular cAMP levels. We identified conserved EREs for OPN, CHMP1A, SNX7 and PSAP and PREs for SNX7. We conclude that GnRH analogues appear not to have major direct effects on gene expression of human endometrial epithelial cells in vitro.
Fil: Zhang, Xiaomei. Eastern Virginia Medical School; Estados Unidos
Fil: Bocca, Silvina. Eastern Virginia Medical School; Estados Unidos
Fil: Franchi, Nilda Anahi. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Investigaciones Biológicas y Tecnológicas. Universidad Nacional de Córdoba. Facultad de Ciencias Exactas, Físicas y Naturales. Instituto de Investigaciones Biológicas y Tecnológicas; Argentina
Fil: Anderson, Sandra. Eastern Virginia Medical School; Estados Unidos
Fil: Kaur, Mandeep. King Abdullah University of Science and Technology; Arabia Saudita
Fil: Bajic, Vladimir B.. King Abdullah University of Science and Technology; Arabia Saudita
Fil: Oehninger, Sergio. Eastern Virginia Medical School; Estados Unidos
Materia
Gene Expression
Ishikawa Cells
Endometrium
Gnrh
Nivel de accesibilidad
acceso abierto
Condiciones de uso
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
Repositorio
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/43009

id CONICETDig_064d95a28044c511e239a7fa9241b1f7
oai_identifier_str oai:ri.conicet.gov.ar:11336/43009
network_acronym_str CONICETDig
repository_id_str 3498
network_name_str CONICET Digital (CONICET)
spelling Do GnRH analogues directly affect human endometrial epithelial cell gene expression?Zhang, XiaomeiBocca, SilvinaFranchi, Nilda AnahiAnderson, SandraKaur, MandeepBajic, Vladimir B.Oehninger, SergioGene ExpressionIshikawa CellsEndometriumGnrhhttps://purl.org/becyt/ford/1.6https://purl.org/becyt/ford/1We examined whether Gonadotrophin-releasing hormone (GnRH) analogues [leuprolide acetate (LA) and ganirelix acetate (GA)] modulate gene expression in Ishikawa cells used as surrogate for human endometrial epithelial cells in vitro. The specific aims were: (i) to study the modulatory effect of GnRH analogues by RT –PCR [in the absence and presence of E2 and P4, and cyclic adenosine monophosphate (cAMP)] on mRNA expression of genes modulated during the window of implantation in GnRH analogues/rFSH-treated assisted reproductive technology cycles including OPTINEURIN (OPTN), CHROMATIN MODIFYING PROTEIN (CHMP1A), PROSAPOSIN (PSAP), IGFBP-5 and SORTING NEXIN 7 (SNX7), and (ii) to analyze the 5′ -flanking regions of such genes for the presence of putative steroid-response elements [estrogen-response elements (EREs) and P4-response element (PREs)]. Ishikawa cells were cytokeratin+/vimentin2 and expressed ERa, ERb, PR and GnRH-R proteins. At 6 and 24 h, neither LA nor GA alone had an effect on gene expression. GnRH analogues alone or following E2 and/or P4 co-incubation for 24 h also had no effect on gene expression, but P4 significantly increased expression of CHMP1A. E2 + P4 treatment for 4 days, alone or followed by GA, had no effect, but E2 + P4 treatment followed by LA significantly decreased IGFBP-5 expression. The addition of 8-Br cAMP did not modify gene expression, with the exception of IGFBP-5 that was significantly increased. The GnRH analogues did not modify intracellular cAMP levels. We identified conserved EREs for OPN, CHMP1A, SNX7 and PSAP and PREs for SNX7. We conclude that GnRH analogues appear not to have major direct effects on gene expression of human endometrial epithelial cells in vitro.Fil: Zhang, Xiaomei. Eastern Virginia Medical School; Estados UnidosFil: Bocca, Silvina. Eastern Virginia Medical School; Estados UnidosFil: Franchi, Nilda Anahi. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Investigaciones Biológicas y Tecnológicas. Universidad Nacional de Córdoba. Facultad de Ciencias Exactas, Físicas y Naturales. Instituto de Investigaciones Biológicas y Tecnológicas; ArgentinaFil: Anderson, Sandra. Eastern Virginia Medical School; Estados UnidosFil: Kaur, Mandeep. King Abdullah University of Science and Technology; Arabia SauditaFil: Bajic, Vladimir B.. King Abdullah University of Science and Technology; Arabia SauditaFil: Oehninger, Sergio. Eastern Virginia Medical School; Estados UnidosOxford University Press2010-06info: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/11336/43009Zhang, Xiaomei; Bocca, Silvina; Franchi, Nilda Anahi; Anderson, Sandra; Kaur, Mandeep; et al.; Do GnRH analogues directly affect human endometrial epithelial cell gene expression?; Oxford University Press; Molecular Human Reproduction; 16; 5; 6-2010; 347-3601360-99471460-2407CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://academic.oup.com/molehr/article/16/5/347/1060836info:eu-repo/semantics/altIdentifier/doi/10.1093/molehr/gaq012info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-29T09:42:15Zoai:ri.conicet.gov.ar:11336/43009instacron: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 09:42:16.13CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv Do GnRH analogues directly affect human endometrial epithelial cell gene expression?
title Do GnRH analogues directly affect human endometrial epithelial cell gene expression?
spellingShingle Do GnRH analogues directly affect human endometrial epithelial cell gene expression?
Zhang, Xiaomei
Gene Expression
Ishikawa Cells
Endometrium
Gnrh
title_short Do GnRH analogues directly affect human endometrial epithelial cell gene expression?
title_full Do GnRH analogues directly affect human endometrial epithelial cell gene expression?
title_fullStr Do GnRH analogues directly affect human endometrial epithelial cell gene expression?
title_full_unstemmed Do GnRH analogues directly affect human endometrial epithelial cell gene expression?
title_sort Do GnRH analogues directly affect human endometrial epithelial cell gene expression?
dc.creator.none.fl_str_mv Zhang, Xiaomei
Bocca, Silvina
Franchi, Nilda Anahi
Anderson, Sandra
Kaur, Mandeep
Bajic, Vladimir B.
Oehninger, Sergio
author Zhang, Xiaomei
author_facet Zhang, Xiaomei
Bocca, Silvina
Franchi, Nilda Anahi
Anderson, Sandra
Kaur, Mandeep
Bajic, Vladimir B.
Oehninger, Sergio
author_role author
author2 Bocca, Silvina
Franchi, Nilda Anahi
Anderson, Sandra
Kaur, Mandeep
Bajic, Vladimir B.
Oehninger, Sergio
author2_role author
author
author
author
author
author
dc.subject.none.fl_str_mv Gene Expression
Ishikawa Cells
Endometrium
Gnrh
topic Gene Expression
Ishikawa Cells
Endometrium
Gnrh
purl_subject.fl_str_mv https://purl.org/becyt/ford/1.6
https://purl.org/becyt/ford/1
dc.description.none.fl_txt_mv We examined whether Gonadotrophin-releasing hormone (GnRH) analogues [leuprolide acetate (LA) and ganirelix acetate (GA)] modulate gene expression in Ishikawa cells used as surrogate for human endometrial epithelial cells in vitro. The specific aims were: (i) to study the modulatory effect of GnRH analogues by RT –PCR [in the absence and presence of E2 and P4, and cyclic adenosine monophosphate (cAMP)] on mRNA expression of genes modulated during the window of implantation in GnRH analogues/rFSH-treated assisted reproductive technology cycles including OPTINEURIN (OPTN), CHROMATIN MODIFYING PROTEIN (CHMP1A), PROSAPOSIN (PSAP), IGFBP-5 and SORTING NEXIN 7 (SNX7), and (ii) to analyze the 5′ -flanking regions of such genes for the presence of putative steroid-response elements [estrogen-response elements (EREs) and P4-response element (PREs)]. Ishikawa cells were cytokeratin+/vimentin2 and expressed ERa, ERb, PR and GnRH-R proteins. At 6 and 24 h, neither LA nor GA alone had an effect on gene expression. GnRH analogues alone or following E2 and/or P4 co-incubation for 24 h also had no effect on gene expression, but P4 significantly increased expression of CHMP1A. E2 + P4 treatment for 4 days, alone or followed by GA, had no effect, but E2 + P4 treatment followed by LA significantly decreased IGFBP-5 expression. The addition of 8-Br cAMP did not modify gene expression, with the exception of IGFBP-5 that was significantly increased. The GnRH analogues did not modify intracellular cAMP levels. We identified conserved EREs for OPN, CHMP1A, SNX7 and PSAP and PREs for SNX7. We conclude that GnRH analogues appear not to have major direct effects on gene expression of human endometrial epithelial cells in vitro.
Fil: Zhang, Xiaomei. Eastern Virginia Medical School; Estados Unidos
Fil: Bocca, Silvina. Eastern Virginia Medical School; Estados Unidos
Fil: Franchi, Nilda Anahi. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Investigaciones Biológicas y Tecnológicas. Universidad Nacional de Córdoba. Facultad de Ciencias Exactas, Físicas y Naturales. Instituto de Investigaciones Biológicas y Tecnológicas; Argentina
Fil: Anderson, Sandra. Eastern Virginia Medical School; Estados Unidos
Fil: Kaur, Mandeep. King Abdullah University of Science and Technology; Arabia Saudita
Fil: Bajic, Vladimir B.. King Abdullah University of Science and Technology; Arabia Saudita
Fil: Oehninger, Sergio. Eastern Virginia Medical School; Estados Unidos
description We examined whether Gonadotrophin-releasing hormone (GnRH) analogues [leuprolide acetate (LA) and ganirelix acetate (GA)] modulate gene expression in Ishikawa cells used as surrogate for human endometrial epithelial cells in vitro. The specific aims were: (i) to study the modulatory effect of GnRH analogues by RT –PCR [in the absence and presence of E2 and P4, and cyclic adenosine monophosphate (cAMP)] on mRNA expression of genes modulated during the window of implantation in GnRH analogues/rFSH-treated assisted reproductive technology cycles including OPTINEURIN (OPTN), CHROMATIN MODIFYING PROTEIN (CHMP1A), PROSAPOSIN (PSAP), IGFBP-5 and SORTING NEXIN 7 (SNX7), and (ii) to analyze the 5′ -flanking regions of such genes for the presence of putative steroid-response elements [estrogen-response elements (EREs) and P4-response element (PREs)]. Ishikawa cells were cytokeratin+/vimentin2 and expressed ERa, ERb, PR and GnRH-R proteins. At 6 and 24 h, neither LA nor GA alone had an effect on gene expression. GnRH analogues alone or following E2 and/or P4 co-incubation for 24 h also had no effect on gene expression, but P4 significantly increased expression of CHMP1A. E2 + P4 treatment for 4 days, alone or followed by GA, had no effect, but E2 + P4 treatment followed by LA significantly decreased IGFBP-5 expression. The addition of 8-Br cAMP did not modify gene expression, with the exception of IGFBP-5 that was significantly increased. The GnRH analogues did not modify intracellular cAMP levels. We identified conserved EREs for OPN, CHMP1A, SNX7 and PSAP and PREs for SNX7. We conclude that GnRH analogues appear not to have major direct effects on gene expression of human endometrial epithelial cells in vitro.
publishDate 2010
dc.date.none.fl_str_mv 2010-06
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/11336/43009
Zhang, Xiaomei; Bocca, Silvina; Franchi, Nilda Anahi; Anderson, Sandra; Kaur, Mandeep; et al.; Do GnRH analogues directly affect human endometrial epithelial cell gene expression?; Oxford University Press; Molecular Human Reproduction; 16; 5; 6-2010; 347-360
1360-9947
1460-2407
CONICET Digital
CONICET
url http://hdl.handle.net/11336/43009
identifier_str_mv Zhang, Xiaomei; Bocca, Silvina; Franchi, Nilda Anahi; Anderson, Sandra; Kaur, Mandeep; et al.; Do GnRH analogues directly affect human endometrial epithelial cell gene expression?; Oxford University Press; Molecular Human Reproduction; 16; 5; 6-2010; 347-360
1360-9947
1460-2407
CONICET Digital
CONICET
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/url/https://academic.oup.com/molehr/article/16/5/347/1060836
info:eu-repo/semantics/altIdentifier/doi/10.1093/molehr/gaq012
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 Oxford University Press
publisher.none.fl_str_mv Oxford University Press
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)
instname_str 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
_version_ 1844613332046184448
score 13.070432