Glioma Stem Cells: Signaling, Microenvironment, and Therapy

被引:144
作者
Liebelt, Brandon D. [1 ,2 ]
Shingu, Takashi [3 ]
Zhou, Xin [3 ]
Ren, Jiangong [3 ]
Shin, Seul A. [3 ]
Hu, Jian [3 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Neurosurg, Houston, TX 77030 USA
[2] Houston Methodist Neurol Inst, Dept Neurosurg, Houston, TX 77030 USA
[3] Univ Texas MD Anderson Canc Ctr, Dept Canc Biol, Houston, TX 77030 USA
关键词
DNA-DAMAGE RESPONSE; SONIC HEDGEHOG; VASCULOGENIC MIMICRY; TUMOR ANGIOGENESIS; HUMAN GLIOBLASTOMA; SELF-RENEWAL; TIE2-EXPRESSING MONOCYTES; CHEMOTHERAPY RESISTANCE; ADJUVANT TEMOZOLOMIDE; SUBEPENDYMAL PLATE;
D O I
10.1155/2016/7849890
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Glioblastoma remains the most common and devastating primary brain tumor despite maximal therapy with surgery, chemotherapy, and radiation. The glioma stem cell (GSC) subpopulation has been identified in glioblastoma and likely plays a key role in resistance of these tumors to conventional therapies as well as recurrent disease. GSCs are capable of self-renewal and differentiation; glioblastoma-derived GSCs are capable of de novo tumor formation when implanted in xenograft models. Further, GSCs possess unique surface markers, modulate characteristic signaling pathways to promote tumorigenesis, and play key roles in glioma vascular formation. These features, in addition to microenvironmental factors, present possible targets for specifically directing therapy against the GSC population within glioblastoma. In this review, the authors summarize the current knowledge of GSC biology and function and the role of GSCs in new vascular formation within glioblastoma and discuss potential therapeutic approaches to target GSCs.
引用
收藏
页数:10
相关论文
共 147 条
[1]   Sonic hedgehog control of size and shape in midbrain pattern formation [J].
Agarwala, S ;
Sanders, TA ;
Ragsdale, CW .
SCIENCE, 2001, 291 (5511) :2147-2150
[2]   Pericytes: Developmental, Physiological, and Pathological Perspectives, Problems, and Promises [J].
Armulik, Annika ;
Genove, Guillem ;
Betsholtz, Christer .
DEVELOPMENTAL CELL, 2011, 21 (02) :193-215
[3]   Notch signaling: Cell fate control and signal integration in development [J].
Artavanis-Tsakonas, S ;
Rand, MD ;
Lake, RJ .
SCIENCE, 1999, 284 (5415) :770-776
[4]   Isolation of putative progenitor endothelial cells for angiogenesis [J].
Asahara, T ;
Murohara, T ;
Sullivan, A ;
Silver, M ;
vanderZee, R ;
Li, T ;
Witzenbichler, B ;
Schatteman, G ;
Isner, JM .
SCIENCE, 1997, 275 (5302) :964-967
[5]  
Atkins R. J., 2012, J CLIN NEUROSCI, V19, P1558
[6]   The role of glioma stem cells in chemotherapy resistance and glioblastoma multiforme recurrence [J].
Auffinger, Brenda ;
Spencer, Drew ;
Pytel, Peter ;
Ahmed, Atique U. ;
Lesniak, Maciej S. .
EXPERT REVIEW OF NEUROTHERAPEUTICS, 2015, 15 (07) :741-752
[7]  
Ayuso-Sacido Angel, 2006, Curr Stem Cell Res Ther, V1, P387
[8]   Activated EGFR signaling increases proliferation, survival, and migration and blocks neuronal differentiation in post-natal neural stem cells [J].
Ayuso-Sacido, Angel ;
Moliterno, Jennifer A. ;
Kratovac, Sebila ;
Kapoor, Gurpreet S. ;
O'Rourke, Donald M. ;
Holland, Eric C. ;
Manuel Garcia-Verdugo, Jose ;
Roy, Neeta S. ;
Boockvar, John A. .
JOURNAL OF NEURO-ONCOLOGY, 2010, 97 (03) :323-337
[9]   Role of microglia in glioma biology [J].
Badie, B ;
Schartner, J .
MICROSCOPY RESEARCH AND TECHNIQUE, 2001, 54 (02) :106-113
[10]   Hedgehog signaling in the subventricular zone is required for both the maintenance of stem cells and the migration of newborn neurons [J].
Balordi, Francesca ;
Fishell, Gord .
JOURNAL OF NEUROSCIENCE, 2007, 27 (22) :5936-5947