Biological and clinical implications of cancer stem cells in primary brain tumors
Despite therapeutic advances, glioblastoma multiforme (GBM) remains a lethal disease. The infiltrative nature of this disease and the presence of a cellular population resistant to current medical treatments account for the poor prognosis of these patients. Growing evidence indicates the existence o...
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doaj-3bd898bf863f448ab09a1382aa6e36e42020-11-24T23:31:42ZengFrontiers Media S.A.Frontiers in Oncology2234-943X2013-01-01310.3389/fonc.2013.0000640744Biological and clinical implications of cancer stem cells in primary brain tumorsMarcello eMaugeri-Saccà0Simona edi Martino1Ruggero eDe Maria2“Regina Elena” National Cancer Institute“Regina Elena” National Cancer Institute“Regina Elena” National Cancer InstituteDespite therapeutic advances, glioblastoma multiforme (GBM) remains a lethal disease. The infiltrative nature of this disease and the presence of a cellular population resistant to current medical treatments account for the poor prognosis of these patients. Growing evidence indicates the existence of a fraction of cancer cells sharing the functional properties of adult stem cells, including self-renewal and a greater ability to escape chemo-radiotherapy-induced death stimuli. Therefore, these cells are commonly defined as cancer stem cells (GBM-SCs). The initial GBM-SC concept has been challenged, and refined according to the emerging molecular taxonomy of GBM. This allowed to postulate the existence of multiple CSC types, each one driving a given molecular entity. Furthermore, it is becoming increasingly clear that GBM-SCs thrive through a dynamic and bidirectional interaction with the surrounding microenvironment. In this article, we discuss recent advances in GBM-SC biology, mechanisms through which these cells adapt to hostile conditions, pharmacological strategies for selectively killing GBM-SCs, and how novel CSC-associated endpoints have been investigated in the clinical setting.http://journal.frontiersin.org/Journal/10.3389/fonc.2013.00006/fullhypoxiacancer stem cellsGlioblastoma Multiformechemo-radioresistancecanonical pathway inhibitorsself-renewal pathway inhibitors |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Marcello eMaugeri-Saccà Simona edi Martino Ruggero eDe Maria |
spellingShingle |
Marcello eMaugeri-Saccà Simona edi Martino Ruggero eDe Maria Biological and clinical implications of cancer stem cells in primary brain tumors Frontiers in Oncology hypoxia cancer stem cells Glioblastoma Multiforme chemo-radioresistance canonical pathway inhibitors self-renewal pathway inhibitors |
author_facet |
Marcello eMaugeri-Saccà Simona edi Martino Ruggero eDe Maria |
author_sort |
Marcello eMaugeri-Saccà |
title |
Biological and clinical implications of cancer stem cells in primary brain tumors |
title_short |
Biological and clinical implications of cancer stem cells in primary brain tumors |
title_full |
Biological and clinical implications of cancer stem cells in primary brain tumors |
title_fullStr |
Biological and clinical implications of cancer stem cells in primary brain tumors |
title_full_unstemmed |
Biological and clinical implications of cancer stem cells in primary brain tumors |
title_sort |
biological and clinical implications of cancer stem cells in primary brain tumors |
publisher |
Frontiers Media S.A. |
series |
Frontiers in Oncology |
issn |
2234-943X |
publishDate |
2013-01-01 |
description |
Despite therapeutic advances, glioblastoma multiforme (GBM) remains a lethal disease. The infiltrative nature of this disease and the presence of a cellular population resistant to current medical treatments account for the poor prognosis of these patients. Growing evidence indicates the existence of a fraction of cancer cells sharing the functional properties of adult stem cells, including self-renewal and a greater ability to escape chemo-radiotherapy-induced death stimuli. Therefore, these cells are commonly defined as cancer stem cells (GBM-SCs). The initial GBM-SC concept has been challenged, and refined according to the emerging molecular taxonomy of GBM. This allowed to postulate the existence of multiple CSC types, each one driving a given molecular entity. Furthermore, it is becoming increasingly clear that GBM-SCs thrive through a dynamic and bidirectional interaction with the surrounding microenvironment. In this article, we discuss recent advances in GBM-SC biology, mechanisms through which these cells adapt to hostile conditions, pharmacological strategies for selectively killing GBM-SCs, and how novel CSC-associated endpoints have been investigated in the clinical setting. |
topic |
hypoxia cancer stem cells Glioblastoma Multiforme chemo-radioresistance canonical pathway inhibitors self-renewal pathway inhibitors |
url |
http://journal.frontiersin.org/Journal/10.3389/fonc.2013.00006/full |
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