Tamoxifen treatment of breast cancer cells : Impact on Hedgehog/GLI1 signaling

The selective estrogen receptor (ER) modulator tamoxifen (TAM) has become the standard therapy for the treatment of ER+ breast cancer patients. Despite the obvious benefits of TAM, a proportion of patients acquire resistance to treatment, and this is a significant clinical problem. Consequently, the...

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Tipo de recurso:
Fecha de publicación:
2016
Institución:
Universidad del Rosario
Repositorio:
Repositorio EdocUR - U. Rosario
Idioma:
eng
OAI Identifier:
oai:repository.urosario.edu.co:10336/21353
Acceso en línea:
https://doi.org/10.3390/ijms17030308
https://repository.urosario.edu.co/handle/10336/21353
Palabra clave:
Hormona antineoplásica
Proteína GLI1
Tamoxifeno factor de transcripcion
Factor de transcripción Gli1
Cancer de mama
Enfermedades
Sonic hedgehog protein
Transcription factor Gli1
Antineoplastic hormone agonists and antagonists
Sonic hedgehog protein
Transcription factor
Transcription factor Gli1
human
GLI1 protein
Neoplasias
Tamoxifeno
Rights
License
Abierto (Texto Completo)
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spelling 315275506008fee86f9-6e55-442a-b5c9-289c56bb75a8600a0931f96-cbc1-4b6a-957c-fbdbc1198cf360093cdcd0f-f4c6-44e2-b0a5-9930b6f34677600550a05db-8308-4ff2-9dbd-157d65a79f476008e474073-64ec-418e-a7ab-8335f150f5e06004cde5d58-abfa-4474-9421-4efdce39d3d86002020-04-01T15:25:42Z2020-04-01T15:25:42Z20162016The selective estrogen receptor (ER) modulator tamoxifen (TAM) has become the standard therapy for the treatment of ER+ breast cancer patients. Despite the obvious benefits of TAM, a proportion of patients acquire resistance to treatment, and this is a significant clinical problem. Consequently, the identification of possible mechanisms involved in TAM-resistance should help the development of new therapeutic targets. In this study, we present in vitro data using a panel of different breast cancer cell lines and demonstrate the modulatory effect of TAM on cellular proliferation and expression of Hedgehog signaling components, including the terminal effector of the pathway, the transcription factor GLI1. A variable pattern of expression following TAM administration was observed, reflecting the distinctive properties of the ER+ and ER´ cell lines analyzed. Remarkably, the TAM-induced increase in the proliferation of the ER+ ZR-75-1 and BT474 cells parallels a sustained upregulation of GLI1 expression and its translocation to the nucleus. These findings, implicating a TAM-GLI1 signaling cross-talk, could ultimately be exploited not only as a means for novel prognostication markers but also in efforts to effectively target breast cancer subtypes. © 2016 by the authors; licensee MDPI, Basel, Switzerland.application/pdfhttps://doi.org/10.3390/ijms170303081661-6596https://repository.urosario.edu.co/handle/10336/21353engNo. 3International Journal of Molecular SciencesVol. 17International Journal of Molecular Sciences, ISSN: 1661-6596 Vol. 17, No. 3 (2016)https://www.mdpi.com/1422-0067/17/3/308Abierto (Texto Completo)http://purl.org/coar/access_right/c_abf2instname:Universidad del Rosarioreponame:Repositorio Institucional EdocURHormona antineoplásicaProteína GLI1Tamoxifeno factor de transcripcionFactor de transcripción Gli1Cancer de mamaEnfermedades616600Sonic hedgehog proteinTranscription factor Gli1Antineoplastic hormone agonists and antagonistsSonic hedgehog proteinTranscription factorTranscription factor Gli1humanGLI1 proteinNeoplasiasTamoxifenoTamoxifen treatment of breast cancer cells : Impact on Hedgehog/GLI1 signalingarticleArtículohttp://purl.org/coar/version/c_970fb48d4fbd8a85http://purl.org/coar/resource_type/c_6501Villegas Gálvez, Victoria EugeniaRondón Lagos, MilenaAnnaratone, LauraCastellano, isabellaGrismaldo, AdrianaSapino, AnnaZaphiropoulos, PeterVillegas, Victoria E.Rondón-Lagos, MilenaAnnaratone, LauraCastellano, IsabellaGrismaldo, AdrianaSapino, AnnaZaphiropoulos, Peter G.ORIGINALTamoxifen_treatment_of_breast_cancer_cells.pdfapplication/pdf4052981https://repository.urosario.edu.co/bitstreams/fa238389-6623-420b-b596-0e13f298e159/download3479bef6bebd92a9d98a15c13dea5b32MD51TEXTTamoxifen_treatment_of_breast_cancer_cells.pdf.txtTamoxifen_treatment_of_breast_cancer_cells.pdf.txtExtracted texttext/plain39599https://repository.urosario.edu.co/bitstreams/4ceac09d-ee72-493f-87a0-8100b3cfe0de/download21d83fa86034d77eae73ef7327c7ef3cMD52THUMBNAILTamoxifen_treatment_of_breast_cancer_cells.pdf.jpgTamoxifen_treatment_of_breast_cancer_cells.pdf.jpgGenerated Thumbnailimage/jpeg4809https://repository.urosario.edu.co/bitstreams/cec9f97c-7448-4bc8-a347-04323ba5a95d/downloadaaa2c4899d4f42f4b196708f3d291e0fMD5310336/21353oai:repository.urosario.edu.co:10336/213532020-05-13 14:48:46.478https://repository.urosario.edu.coRepositorio institucional EdocURedocur@urosario.edu.co
dc.title.spa.fl_str_mv Tamoxifen treatment of breast cancer cells : Impact on Hedgehog/GLI1 signaling
title Tamoxifen treatment of breast cancer cells : Impact on Hedgehog/GLI1 signaling
spellingShingle Tamoxifen treatment of breast cancer cells : Impact on Hedgehog/GLI1 signaling
Hormona antineoplásica
Proteína GLI1
Tamoxifeno factor de transcripcion
Factor de transcripción Gli1
Cancer de mama
Enfermedades
Sonic hedgehog protein
Transcription factor Gli1
Antineoplastic hormone agonists and antagonists
Sonic hedgehog protein
Transcription factor
Transcription factor Gli1
human
GLI1 protein
Neoplasias
Tamoxifeno
title_short Tamoxifen treatment of breast cancer cells : Impact on Hedgehog/GLI1 signaling
title_full Tamoxifen treatment of breast cancer cells : Impact on Hedgehog/GLI1 signaling
title_fullStr Tamoxifen treatment of breast cancer cells : Impact on Hedgehog/GLI1 signaling
title_full_unstemmed Tamoxifen treatment of breast cancer cells : Impact on Hedgehog/GLI1 signaling
title_sort Tamoxifen treatment of breast cancer cells : Impact on Hedgehog/GLI1 signaling
dc.subject.spa.fl_str_mv Hormona antineoplásica
Proteína GLI1
Tamoxifeno factor de transcripcion
Factor de transcripción Gli1
Cancer de mama
topic Hormona antineoplásica
Proteína GLI1
Tamoxifeno factor de transcripcion
Factor de transcripción Gli1
Cancer de mama
Enfermedades
Sonic hedgehog protein
Transcription factor Gli1
Antineoplastic hormone agonists and antagonists
Sonic hedgehog protein
Transcription factor
Transcription factor Gli1
human
GLI1 protein
Neoplasias
Tamoxifeno
dc.subject.ddc.spa.fl_str_mv Enfermedades
dc.subject.keyword.spa.fl_str_mv Sonic hedgehog protein
Transcription factor Gli1
Antineoplastic hormone agonists and antagonists
Sonic hedgehog protein
Transcription factor
Transcription factor Gli1
dc.subject.keyword.eng.fl_str_mv human
GLI1 protein
dc.subject.lemb.spa.fl_str_mv Neoplasias
Tamoxifeno
description The selective estrogen receptor (ER) modulator tamoxifen (TAM) has become the standard therapy for the treatment of ER+ breast cancer patients. Despite the obvious benefits of TAM, a proportion of patients acquire resistance to treatment, and this is a significant clinical problem. Consequently, the identification of possible mechanisms involved in TAM-resistance should help the development of new therapeutic targets. In this study, we present in vitro data using a panel of different breast cancer cell lines and demonstrate the modulatory effect of TAM on cellular proliferation and expression of Hedgehog signaling components, including the terminal effector of the pathway, the transcription factor GLI1. A variable pattern of expression following TAM administration was observed, reflecting the distinctive properties of the ER+ and ER´ cell lines analyzed. Remarkably, the TAM-induced increase in the proliferation of the ER+ ZR-75-1 and BT474 cells parallels a sustained upregulation of GLI1 expression and its translocation to the nucleus. These findings, implicating a TAM-GLI1 signaling cross-talk, could ultimately be exploited not only as a means for novel prognostication markers but also in efforts to effectively target breast cancer subtypes. © 2016 by the authors; licensee MDPI, Basel, Switzerland.
publishDate 2016
dc.date.created.none.fl_str_mv 2016
dc.date.issued.none.fl_str_mv 2016
dc.date.accessioned.none.fl_str_mv 2020-04-01T15:25:42Z
dc.date.available.none.fl_str_mv 2020-04-01T15:25:42Z
dc.type.eng.fl_str_mv article
dc.type.coarversion.fl_str_mv http://purl.org/coar/version/c_970fb48d4fbd8a85
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dc.type.spa.spa.fl_str_mv Artículo
dc.identifier.doi.none.fl_str_mv https://doi.org/10.3390/ijms17030308
dc.identifier.issn.none.fl_str_mv 1661-6596
dc.identifier.uri.none.fl_str_mv https://repository.urosario.edu.co/handle/10336/21353
url https://doi.org/10.3390/ijms17030308
https://repository.urosario.edu.co/handle/10336/21353
identifier_str_mv 1661-6596
dc.language.iso.spa.fl_str_mv eng
language eng
dc.relation.citationIssue.none.fl_str_mv No. 3
dc.relation.citationTitle.none.fl_str_mv International Journal of Molecular Sciences
dc.relation.citationVolume.none.fl_str_mv Vol. 17
dc.relation.ispartof.spa.fl_str_mv International Journal of Molecular Sciences, ISSN: 1661-6596 Vol. 17, No. 3 (2016)
dc.relation.uri.spa.fl_str_mv https://www.mdpi.com/1422-0067/17/3/308
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dc.rights.acceso.spa.fl_str_mv Abierto (Texto Completo)
rights_invalid_str_mv Abierto (Texto Completo)
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institution Universidad del Rosario
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