Kim Won Jong, Yockman James W, Lee Minhyung, Jeong Ji Hoon, Kim Yong-Hee, Kim Sung Wan
Center for Controlled Chemical Delivery, Department of Pharmaceutics and Pharmaceutical Chemistry, 30 S 2000 E RM 201, University of Utah, Salt Lake City, UT 84112-5820, USA.
J Control Release. 2005 Aug 18;106(1-2):224-34. doi: 10.1016/j.jconrel.2005.04.016.
Vascular endothelial growth factor (VEGF), a potent angiogenic molecule specific for vascular endothelial cells, is overexpressed in most tumors and closely associated with tumor growth and metastasis. It has been shown that a soluble fragment of VEGF receptor Flt-1 (sFlt-1) has anti-angiogenic properties by way of its antagonist activity against VEGF. In the present study, we demonstrated that the stable expression of sFlt-1 by endothelial cell targeted non-viral gene delivery inhibited the angiogenesis of endothelial cells. A targeted polymeric gene delivery system, PEI-g-PEG-RGD, was developed by incorporating the alphanubeta3/alphanubeta5 integrin-binding RGD peptide, ACDCRGDCFC (single-letter amino acid code), into the cationic polymer, polyethylenimine (PEI) via a hydrophilic polyethylene glycol (PEG) spacer. The functional analysis of therapeutic gene encoding sFlt-1/carrier complex was performed with an endothelial cell proliferation assay. The complex of sFlt-1 gene with PEI-g-PEG-RGD conjugate efficiently inhibited the proliferation of cultured endothelial cells, representing that expressed sFlt-1 predominantly bound to exogenous VEGF and blocked the binding of VEGF to the full-length Flt-1 receptor. These findings suggest that the combination of targeted gene carrier and sFlt-1 possesses the potential to be an efficient tool for the anti-angiogenic gene therapy to treat cancer.
血管内皮生长因子(VEGF)是一种对血管内皮细胞具有特异性的强效血管生成分子,在大多数肿瘤中过度表达,且与肿瘤生长和转移密切相关。研究表明,VEGF受体Flt-1的可溶性片段(sFlt-1)通过其对VEGF的拮抗活性具有抗血管生成特性。在本研究中,我们证明了通过内皮细胞靶向非病毒基因递送实现sFlt-1的稳定表达可抑制内皮细胞的血管生成。通过将αβ3/αβ5整合素结合RGD肽ACDCRGDCFC(单字母氨基酸代码)经亲水性聚乙二醇(PEG)间隔基团掺入阳离子聚合物聚乙烯亚胺(PEI)中,开发了一种靶向聚合物基因递送系统PEI-g-PEG-RGD。利用内皮细胞增殖试验对编码sFlt-1/载体复合物的治疗性基因进行功能分析。sFlt-1基因与PEI-g-PEG-RGD缀合物的复合物有效抑制了培养的内皮细胞的增殖,这表明表达的sFlt-1主要与外源性VEGF结合,并阻断了VEGF与全长Flt-1受体的结合。这些发现表明,靶向基因载体与sFlt-1的组合具有成为治疗癌症的抗血管生成基因治疗有效工具的潜力。