Vessel co-option in glioblastoma: emerging insights and opportunities

被引:99
作者
Seano, Giorgio [1 ]
Jain, Rakesh K. [2 ,3 ]
机构
[1] PSL Res Univ, Tumor Microenvironm Lab, Paris Saclay Univ, Res Ctr,Inst Curie,Inserm U1021,CNRS,UMR3347, F-91405 Orsay, France
[2] Massachusetts Gen Hosp, Edwin L Steele Lab, Dept Radiat Oncol, Boston, MA 02114 USA
[3] Harvard Med Sch, Boston, MA 02114 USA
基金
欧洲研究理事会;
关键词
Vessel co-option; Glioblastoma; Anti-angiogenesis; Cell migration; Tumor microenvironment; ENDOTHELIAL GROWTH-FACTOR; NON-ANGIOGENIC TUMORS; FACTOR RECEPTOR; INVASION; CANCER; THERAPY; GLIOMA; METASTASES; CELLS; VASCULARIZATION;
D O I
10.1007/s10456-019-09691-z
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
Vessel co-option is the movement of cancer cells towards and along the pre-existing vasculature and is an alternative to angiogenesis to gain access to nutrients. Vessel co-option has been shown as a strategy employed by some glioblastoma (GBM) cells to invade further into the brain, leading to one of the greatest challenges in treating GBM. In GBM, vessel co-option may be an intrinsic feature or an acquired mechanism of resistance to anti-angiogenic treatment. Here, we describe the histological features and the dynamics visualized through intravital microscopy of vessel co-option in GBM, as well as the molecular players discovered until now. We also highlight key unanswered questions, as answering these is critical to improve understanding of GBM progression and for developing more effective approaches for GBM treatment.
引用
收藏
页码:9 / 16
页数:8
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