Department of Orthopedics, Hualien Armed Forces Hospital, Hualien, 97144, Taiwan, ROC.
Cytotechnology. 2011 May;63(3):285-93. doi: 10.1007/s10616-011-9340-2. Epub 2011 Apr 3.
Vascular endothelial growth factor (VEGF) promotes the growth of solid tumor mainly via VEGF receptor-1 and receptor-2, which are expressed preferentially in proliferating endothelial cells. Therefore, a strategy for simultaneous blockage of both VEGF receptors may have a useful therapeutic effect in tumor growth. In this study, we utilized a fusion protein which is composed of receptor binding domain of VEGF-A (RBDV) and the constant region fragment (Fc) of a human immunoglobulin G1 (IgG1), to interfere with the growth of human umbilical vein endothelial cells (HUVECs) via VEGF receptors. The results showed that RBDV-IgG1 Fc was able to bind with both VEGF receptor-1 and receptor-2. In addition, RBDV-IgG1 Fc could decrease VEGF-induced proliferation and tube formation among HUVECs. Moreover, the cytotoxic test showed RBDV-IgG1 Fc could also enhance the cytotoxic activity of human natural killing cells. The data are suggesting that the fusion protein, RBDV-IgG1 Fc, may have potential as an angiogenesis antagonist for future tumor therapy.
血管内皮生长因子 (VEGF) 主要通过血管内皮生长因子受体-1 和受体-2 促进实体瘤的生长,而这两种受体在增殖的内皮细胞中优先表达。因此,同时阻断两种 VEGF 受体的策略可能对肿瘤生长具有有用的治疗效果。在这项研究中,我们利用一种融合蛋白,该蛋白由 VEGF-A 的受体结合域 (RBDV) 和人免疫球蛋白 G1 (IgG1) 的恒定区片段 (Fc) 组成,通过 VEGF 受体来干扰人脐静脉内皮细胞 (HUVEC) 的生长。结果表明,RBDV-IgG1 Fc 能够与 VEGF 受体-1 和受体-2 结合。此外,RBDV-IgG1 Fc 可以降低 VEGF 诱导的 HUVEC 增殖和管形成。此外,细胞毒性试验表明,RBDV-IgG1 Fc 还可以增强人自然杀伤细胞的细胞毒性活性。这些数据表明,融合蛋白 RBDV-IgG1 Fc 可能具有作为未来肿瘤治疗的血管生成拮抗剂的潜力。