The perivascular niche microenvironment in brain tumor progression

被引:138
作者
Charles, Nikki [1 ,2 ]
Holland, Eric C. [1 ,2 ,3 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Dept Canc Biol & Genet, New York, NY 10021 USA
[2] Mem Sloan Kettering Canc Ctr, Brain Tumor Ctr, New York, NY 10021 USA
[3] Mem Sloan Kettering Canc Ctr, Dept Neurosurg & Surg, New York, NY 10021 USA
关键词
glioblastoma; perivascular niche; brain tumor; cancer stem-like cells; microenvironment; NEURAL STEM-CELLS; ENDOTHELIAL GROWTH-FACTOR; BLOOD-VESSEL FORMATION; PROTEIN-KINASE B; GLIOMAS IN-VIVO; SONIC-HEDGEHOG; MALIGNANT GLIOMAS; PROGENITOR CELLS; VASCULAR NICHE; NOTCH PATHWAY;
D O I
10.4161/cc.9.15.12710
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Glioblastoma, the most frequent and aggressive malignant brain tumor, has a very poor prognosis of approximately 1-year. The associated aggressive phenotype and therapeutic resistance of glioblastoma is postulated to be due to putative brain tumor stem-like cells (BTSC). The best hope for improved therapy lies in the ability to understand the molecular biology that controls BTSC behavior. The tumor vascular microenvironment of brain tumors has emerged as important regulators of BTSC behavior. Emerging data have identified the vascular microenvironment as home to a multitude of cell types engaged in various signaling that work collectively to foster a supportive environment for BTSCs. Characterization of the signaling pathways and intercellular communication between resident cell types in the microvascular niche of brain tumors is critical to the identification of potential BTSC-specific targets for therapy.
引用
收藏
页码:3012 / 3021
页数:10
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