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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...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2016
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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. |
format | Online Article Text |
id | pubmed-5075570 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
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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