Growth factor-mediated angiogenesis in the malignant progression of glial tumors: A review

被引:147
作者
Jensen, RL [1 ]
机构
[1] Loyola Univ, Med Ctr, Dept Neurosurg, Maywood, IL 60153 USA
来源
SURGICAL NEUROLOGY | 1998年 / 49卷 / 02期
关键词
glioblastoma multiforme; astrocytoma; angiogenesis; vascular endothelial growth factor; platelet-derived growth factor; fibroblast growth factor; epidermal growth factor; transforming growth factor beta; neovascularization; vascular permeability;
D O I
10.1016/S0090-3019(97)00218-8
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
BACKGROUND We review the role of peptide growth factors in angiogenesis and progression of low grade glial tumors to higher grade glioblastoma multiforme (GEM). METHODS Vascular pathology is a key feature of glioblastoma multiforme characterized by hypervascularity, vascular permeability, and hypercoagulability. RESULTS Vascular endothelial growth factor (VEGF) can mediate all of these effects, but by itself does not promote malignant growth. Epidermal growth factor (EGF), platelet-derived growth factor (PDGF), fibroblast growth factor (FGF), and transforming growth factor beta (TGF-beta) are implicated in the angiogenesis of a number of tumors including those of glial origin. CONCLUSIONS These growth factors are suggested to play a role in autocrine and/or paracrine mediated tumorogenesis of astrocytic tumors. VEGF secretion might be the product of induction by physiologic concentrations of other growth factors with VEGF being the common pathway of neovascularization and progression to GEM. (C) 1998 by Elsevier Science Inc.
引用
收藏
页码:189 / 195
页数:7
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