Cargando…
Cancer stem cells in glioblastoma
Tissues with defined cellular hierarchies in development and homeostasis give rise to tumors with cellular hierarchies, suggesting that tumors recapitulate specific tissues and mimic their origins. Glioblastoma (GBM) is the most prevalent and malignant primary brain tumor and contains self-renewing,...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory Press
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4495393/ https://www.ncbi.nlm.nih.gov/pubmed/26109046 http://dx.doi.org/10.1101/gad.261982.115 |
_version_ | 1782380246803152896 |
---|---|
author | Lathia, Justin D. Mack, Stephen C. Mulkearns-Hubert, Erin E. Valentim, Claudia L.L. Rich, Jeremy N. |
author_facet | Lathia, Justin D. Mack, Stephen C. Mulkearns-Hubert, Erin E. Valentim, Claudia L.L. Rich, Jeremy N. |
author_sort | Lathia, Justin D. |
collection | PubMed |
description | Tissues with defined cellular hierarchies in development and homeostasis give rise to tumors with cellular hierarchies, suggesting that tumors recapitulate specific tissues and mimic their origins. Glioblastoma (GBM) is the most prevalent and malignant primary brain tumor and contains self-renewing, tumorigenic cancer stem cells (CSCs) that contribute to tumor initiation and therapeutic resistance. As normal stem and progenitor cells participate in tissue development and repair, these developmental programs re-emerge in CSCs to support the development and progressive growth of tumors. Elucidation of the molecular mechanisms that govern CSCs has informed the development of novel targeted therapeutics for GBM and other brain cancers. CSCs are not self-autonomous units; rather, they function within an ecological system, both actively remodeling the microenvironment and receiving critical maintenance cues from their niches. To fulfill the future goal of developing novel therapies to collapse CSC dynamics, drawing parallels to other normal and pathological states that are highly interactive with their microenvironments and that use developmental signaling pathways will be beneficial. |
format | Online Article Text |
id | pubmed-4495393 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Cold Spring Harbor Laboratory Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-44953932015-12-15 Cancer stem cells in glioblastoma Lathia, Justin D. Mack, Stephen C. Mulkearns-Hubert, Erin E. Valentim, Claudia L.L. Rich, Jeremy N. Genes Dev Review Tissues with defined cellular hierarchies in development and homeostasis give rise to tumors with cellular hierarchies, suggesting that tumors recapitulate specific tissues and mimic their origins. Glioblastoma (GBM) is the most prevalent and malignant primary brain tumor and contains self-renewing, tumorigenic cancer stem cells (CSCs) that contribute to tumor initiation and therapeutic resistance. As normal stem and progenitor cells participate in tissue development and repair, these developmental programs re-emerge in CSCs to support the development and progressive growth of tumors. Elucidation of the molecular mechanisms that govern CSCs has informed the development of novel targeted therapeutics for GBM and other brain cancers. CSCs are not self-autonomous units; rather, they function within an ecological system, both actively remodeling the microenvironment and receiving critical maintenance cues from their niches. To fulfill the future goal of developing novel therapies to collapse CSC dynamics, drawing parallels to other normal and pathological states that are highly interactive with their microenvironments and that use developmental signaling pathways will be beneficial. Cold Spring Harbor Laboratory Press 2015-06-15 /pmc/articles/PMC4495393/ /pubmed/26109046 http://dx.doi.org/10.1101/gad.261982.115 Text en © 2015 Lathia et al.; Published by Cold Spring Harbor Laboratory Press http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed exclusively by Cold Spring Harbor Laboratory Press for the first six months after the full-issue publication date (see http://genesdev.cshlp.org/site/misc/terms.xhtml). After six months, it is available under a Creative Commons License (Attribution-NonCommercial 4.0 International), as described at http://creativecommons.org/licenses/by-nc/4.0/. |
spellingShingle | Review Lathia, Justin D. Mack, Stephen C. Mulkearns-Hubert, Erin E. Valentim, Claudia L.L. Rich, Jeremy N. Cancer stem cells in glioblastoma |
title | Cancer stem cells in glioblastoma |
title_full | Cancer stem cells in glioblastoma |
title_fullStr | Cancer stem cells in glioblastoma |
title_full_unstemmed | Cancer stem cells in glioblastoma |
title_short | Cancer stem cells in glioblastoma |
title_sort | cancer stem cells in glioblastoma |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4495393/ https://www.ncbi.nlm.nih.gov/pubmed/26109046 http://dx.doi.org/10.1101/gad.261982.115 |
work_keys_str_mv | AT lathiajustind cancerstemcellsinglioblastoma AT mackstephenc cancerstemcellsinglioblastoma AT mulkearnshuberterine cancerstemcellsinglioblastoma AT valentimclaudiall cancerstemcellsinglioblastoma AT richjeremyn cancerstemcellsinglioblastoma |