Brain angiogenesis in developmental and pathological processes: therapeutic aspects of vascular endothelial growth factor

被引:70
|
作者
Shibuya, Masabumi [1 ,2 ]
机构
[1] Tokyo Med & Dent Univ, Dept Mol Oncol, Bunkyo Ku, Tokyo 1138519, Japan
[2] Jobu Univ, Takasaki, Gunma, Japan
基金
日本学术振兴会;
关键词
macrophage; malignant glioma; motor neuron; tumor angiogenesis; vascular hyperpermeability; VEGF-A; VEGF-B; VEGF-E; VEGFR-1; VEGFR-2; INDEPENDENT REGULATION; FACTOR RECEPTOR; VEGF; BEVACIZUMAB; PROMOTES; MACROPHAGES; GLIOMAS; FLT-1; PERMEABILITY; MECHANISMS;
D O I
10.1111/j.1742-4658.2009.07175.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The angiogenic process in the central nervous system (CNS) is basically regulated by typical angiogenic signaling systems such as vascular endothelial growth factor (VEGF)-VEGF receptors and angiopoietin-Tie receptors. In addition to regular endothelial-pericyte interaction, the CNS vasculature has a unique system of cell to cell communication between endothelial cells and astrocytes which is known as the blood-brain barrier. Among the pathological conditions of the CNS vascular network, stroke is a major disease in which the supply of blood is decreased. Pro-angiogenic therapy using natural VEGF-A has so far been unsuccessful, indicating the possible need for a new approach related to upstream or downstream regulators involved in the VEGF-signaling pathway, or alternate VEGF family members. By contrast, a pathological increase in the blood supply in the CNS is seen in brain tumors, in particular malignant gliomas. In phase II clinical trials, anti-VEGF therapies have been shown to suppress tumor growth and improve survival rates to some extent. However, tumor invasion and the distant metastasis of gliomas can occur following anti-angiogenic therapy. Further studies are needed to obtain safer clinical outcomes by developing new strategies with combination therapy using known anti-angiogenic drugs or by developing unique medicines specifically targeting the blood vessels in brain tumors.
引用
收藏
页码:4636 / 4643
页数:8
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