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Targeting SOX2 as a Therapeutic Strategy in Glioblastoma

Glioblastoma is the most common and malignant brain cancer in adults. Current therapy consisting of surgery followed by radiation and temozolomide has a moderate success rate and the tumor reappears. Among the features that a cancer cell must have to survive the therapeutic treatment and reconstitut...

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Autores principales: Garros-Regulez, Laura, Garcia, Idoia, Carrasco-Garcia, Estefania, Lantero, Aquilino, Aldaz, Paula, Moreno-Cugnon, Leire, Arrizabalaga, Olatz, Undabeitia, Jose, Torres-Bayona, Sergio, Villanua, Jorge, Ruiz, Irune, Egaña, Larraitz, Sampron, Nicolas, Matheu, Ander
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5075570/
https://www.ncbi.nlm.nih.gov/pubmed/27822457
http://dx.doi.org/10.3389/fonc.2016.00222
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author Garros-Regulez, Laura
Garcia, Idoia
Carrasco-Garcia, Estefania
Lantero, Aquilino
Aldaz, Paula
Moreno-Cugnon, Leire
Arrizabalaga, Olatz
Undabeitia, Jose
Torres-Bayona, Sergio
Villanua, Jorge
Ruiz, Irune
Egaña, Larraitz
Sampron, Nicolas
Matheu, Ander
author_facet Garros-Regulez, Laura
Garcia, Idoia
Carrasco-Garcia, Estefania
Lantero, Aquilino
Aldaz, Paula
Moreno-Cugnon, Leire
Arrizabalaga, Olatz
Undabeitia, Jose
Torres-Bayona, Sergio
Villanua, Jorge
Ruiz, Irune
Egaña, Larraitz
Sampron, Nicolas
Matheu, Ander
author_sort Garros-Regulez, Laura
collection PubMed
description Glioblastoma is the most common and malignant brain cancer in adults. Current therapy consisting of surgery followed by radiation and temozolomide has a moderate success rate and the tumor reappears. Among the features that a cancer cell must have to survive the therapeutic treatment and reconstitute the tumor is the ability of self-renewal. Therefore, it is vital to identify the molecular mechanisms that regulate this activity. Sex-determining region Y (SRY)-box 2 (SOX2) is a transcription factor whose activity has been associated with the maintenance of the undifferentiated state of cancer stem cells in several tissues, including the brain. Several groups have detected increased SOX2 levels in biopsies of glioblastoma patients, with the highest levels associated with poor outcome. Therefore, SOX2 silencing might be a novel therapeutic approach to combat cancer and particularly brain tumors. In this review, we will summarize the current knowledge about SOX2 in glioblastoma and recapitulate several strategies that have recently been described targeting SOX2 in this malignancy.
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spelling pubmed-50755702016-11-07 Targeting SOX2 as a Therapeutic Strategy in Glioblastoma Garros-Regulez, Laura Garcia, Idoia Carrasco-Garcia, Estefania Lantero, Aquilino Aldaz, Paula Moreno-Cugnon, Leire Arrizabalaga, Olatz Undabeitia, Jose Torres-Bayona, Sergio Villanua, Jorge Ruiz, Irune Egaña, Larraitz Sampron, Nicolas Matheu, Ander Front Oncol Oncology Glioblastoma is the most common and malignant brain cancer in adults. Current therapy consisting of surgery followed by radiation and temozolomide has a moderate success rate and the tumor reappears. Among the features that a cancer cell must have to survive the therapeutic treatment and reconstitute the tumor is the ability of self-renewal. Therefore, it is vital to identify the molecular mechanisms that regulate this activity. Sex-determining region Y (SRY)-box 2 (SOX2) is a transcription factor whose activity has been associated with the maintenance of the undifferentiated state of cancer stem cells in several tissues, including the brain. Several groups have detected increased SOX2 levels in biopsies of glioblastoma patients, with the highest levels associated with poor outcome. Therefore, SOX2 silencing might be a novel therapeutic approach to combat cancer and particularly brain tumors. In this review, we will summarize the current knowledge about SOX2 in glioblastoma and recapitulate several strategies that have recently been described targeting SOX2 in this malignancy. Frontiers Media S.A. 2016-10-24 /pmc/articles/PMC5075570/ /pubmed/27822457 http://dx.doi.org/10.3389/fonc.2016.00222 Text en Copyright © 2016 Garros-Regulez, Garcia, Carrasco-Garcia, Lantero, Aldaz, Moreno-Cugnon, Arrizabalaga, Undabeitia, Torres-Bayona, Villanua, Ruiz, Egaña, Sampron and Matheu. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Garros-Regulez, Laura
Garcia, Idoia
Carrasco-Garcia, Estefania
Lantero, Aquilino
Aldaz, Paula
Moreno-Cugnon, Leire
Arrizabalaga, Olatz
Undabeitia, Jose
Torres-Bayona, Sergio
Villanua, Jorge
Ruiz, Irune
Egaña, Larraitz
Sampron, Nicolas
Matheu, Ander
Targeting SOX2 as a Therapeutic Strategy in Glioblastoma
title Targeting SOX2 as a Therapeutic Strategy in Glioblastoma
title_full Targeting SOX2 as a Therapeutic Strategy in Glioblastoma
title_fullStr Targeting SOX2 as a Therapeutic Strategy in Glioblastoma
title_full_unstemmed Targeting SOX2 as a Therapeutic Strategy in Glioblastoma
title_short Targeting SOX2 as a Therapeutic Strategy in Glioblastoma
title_sort targeting sox2 as a therapeutic strategy in glioblastoma
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5075570/
https://www.ncbi.nlm.nih.gov/pubmed/27822457
http://dx.doi.org/10.3389/fonc.2016.00222
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