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.©2013 Maugeri-Saccà , Di Martino and De Maria.
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.©2013 Maugeri-Saccà , Di Martino and De Maria.
KW - Cancer Research
KW - Cancer stem cells
KW - Canonical pathway inhibitors
KW - Chemo-radioresistance
KW - Differentiation-inducing agents
KW - Glioblastoma multiforme
KW - Hypoxia
KW - Oncology
KW - Self-renewal pathway inhibitors
KW - Stem cell-based endpoints
KW - Cancer Research
KW - Cancer stem cells
KW - Canonical pathway inhibitors
KW - Chemo-radioresistance
KW - Differentiation-inducing agents
KW - Glioblastoma multiforme
KW - Hypoxia
KW - Oncology
KW - Self-renewal pathway inhibitors
KW - Stem cell-based endpoints
UR - http://hdl.handle.net/10807/112115
UR - http://www.frontiersin.org/journal/fulltext.aspx?art_doi=10.3389/fonc.2013.00006&x=y#h15
U2 - 10.3389/fonc.2013.00006
DO - 10.3389/fonc.2013.00006
M3 - Article
SN - 2234-943X
VL - 3
SP - N/A-N/A
JO - Frontiers in Oncology
JF - Frontiers in Oncology
ER -