TY - JOUR
T1 - Biological and clinical implications of cancer stem cells in primary brain tumors
AU - Maugeri-Saccà, Marcello
AU - Di Martino, Simona
AU - De Maria Marchiano, Ruggero
PY - 2013
Y1 - 2013
N2 - 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.
AB - 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.
KW - glioblastoma multiforme, cancer stem cells, chemo-radioresistance, canonical pathway inhibitors, self- renewal pathway inhibitors, differentiation-inducing agents, hypoxia, stem cell-based endpoints
KW - glioblastoma multiforme, cancer stem cells, chemo-radioresistance, canonical pathway inhibitors, self- renewal pathway inhibitors, differentiation-inducing agents, hypoxia, stem cell-based endpoints
UR - http://hdl.handle.net/10807/111512
U2 - 10.3389/fonc.2013.00006
DO - 10.3389/fonc.2013.00006
M3 - Article
SN - 2234-943X
SP - N/A-N/A
JO - Frontiers in Oncology
JF - Frontiers in Oncology
ER -