Selective upregulation of vascular endothelial growth factor receptors neuropilin-1 and-2 in human neuroblastoma

被引:71
|
作者
Fakhari, M
Pullirsch, D
Abraham, D
Paya, K
Hofbauer, R
Holzfeind, P
Hofmann, M
Aharinejad, S
机构
[1] Univ Vienna, Dept Anat, Cardiovasc Res Lab, A-1090 Vienna, Austria
[2] Univ Vienna, Dept Pediat Surg, Vienna, Austria
[3] Univ Vienna, Inst Med Biochem, Dept Mol Biol, Vienna, Austria
[4] Univ Vienna, Dept Anat, Neuromuscular Res Lab, Vienna, Austria
关键词
neuroblastoma; neuropilin; vascular endothelial growth factor; gene expression;
D O I
10.1002/cncr.10177
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND. Recent studies show that vascular endothelial growth factor (VEGF) and its receptors Flt-1 and KDR, and a series of other angiogenic molecules, are upregulated in advanced but not low stage human neuroblastoma. Neuropilin-1 and 2 (NRP) are novel specific receptors of VEGF(165), whose role is unknown in human neuroblastoma. METHODS. Tissue biopsies of 37 cliildren with Stage I-IV neuroblastoma were obtained, as well as biopsies of 7 normal adrenals as controls. The mRNA expression of VEGF(165) and its receptors Flt-1, KDR, NRP1, and NRP2 was evaluated by real-time reverse transcripton polymerase chain reaction. NRP protein expression was detected by immunocytochemistry and Western blotting. RESULTS. VEGF(165) mRNA was Upregulated in Stage III and IV and FIt-1 and KDR gene expression was increased in Stage III, while NRP1 and 2 mRNA and protein levels were higher in Stages I-IV vs. controls (P < 0.05). NRP was expressed in vascular endothelial but nut tumor cells. CONCLUSIONS. These results show fur the first time that human neuroblastoma expresses NRP, and that NRP co-regulates VEGF angiogenic effect in human neuroblastoma. NRP might be a sensitive angiogenic measure of %VEGF systems in neuroblastoma, particularly, in its early stages. (C) 2002 American Cancer Society.
引用
收藏
页码:258 / 263
页数:6
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