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Inhibition of lymphatic metastasis in neuroblastoma by a novel neutralizing antibody to vascular endothelial growth factor‐D

机译:新型抗血管内皮生长因子-D中和抗体抑制神经母细胞瘤淋巴转移

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AbstractLymphatic spread is an important clinical determinant in the prognosis of many human cancers. The lymphangiogenic factor vascular endothelial growth factor-D (VEGF-D) is implicated in the promotion of lymphatic metastasis through the development of lymphatic vessels in some human cancers. In this study, we developed an anti-VEGF-D monoclonal antibody, cVE199, and investigated its in vitro properties, in vivo effects against tumors and possible target indications to evaluate its potential as a therapeutic antibody. The cVE199 molecule was revealed to have a specific binding reactivity against human VEGF-D, as well as a specific inhibitory activity against the binding of human VEGF-D to VEGFR-3. In addition, cVE199 was found to inhibit the biological activity of VEGF-D against lymphatic cells in vitro. Because we determined that a neuroblastoma cell line, SK-N-DZ, abundantly expressed VEGF-D, an in vivo efficacy study was performed using a xenograft model of SK-N-DZ. We found that cVE199 significantly decreased lymphatic metastasis of SK-N-DZ as well as lymphangiogenesis in primary lesions. Finally, we investigated VEGF-D expression in human neuroblastoma, finding that the molecule was expressed in 11 of 29 human neuroblastoma specimens (37.9%). In conclusion, we found that a novel anti-VEGF-D monoclonal antibody, cVE199, with specific reactivity against human VEGF-D, prevents lymphatic metastasis of neuroblastoma through the inhibition of lymphangiogenesis in an animal model. In addition, our results show that VEGF-D is expressed in some cases of human neuroblastomas, which suggests that cVE199 is a potential anti-metastasis therapeutic antibody in neuroblastoma treatment.
机译:摘要淋巴管扩散是许多人类癌症预后的重要临床决定因素。在某些人类癌症中,淋巴管生成因子血管内皮生长因子-D(VEGF-D)参与通过淋巴管的发育促进淋巴转移。在这项研究中,我们开发了抗VEGF-D单克隆抗体cVE199,并研究了其体外特性,对肿瘤的体内作用以及可能的靶标以评估其作为治疗性抗体的潜力。揭示了cVE199分子具有针对人VEGF-D的特异性结合反应,以及针对人VEGF-D与VEGFR-3的结合的特异性抑制活性。此外,发现cVE199在体外抑制VEGF-D对淋巴细胞的生物学活性。因为我们确定神经母细胞瘤细胞系SK-N-DZ大量表达VEGF-D,所以使用SK-N-DZ异种移植模型进行了体内功效研究。我们发现cVE199显着降低了SK-N-DZ的淋巴转移以及原发灶中的淋巴管生成。最后,我们研究了人神经母细胞瘤中VEGF-D的表达,发现该分子在29个人神经母细胞瘤样本中的11个(37.9%)中表达。总之,我们发现一种新型抗VEGF-D单克隆抗体cVE199对人VEGF-D具有特异性反应,可通过抑制动物模型中的淋巴管生成来防止神经母细胞瘤的淋巴转移。此外,我们的结果表明,VEGF-D在某些人类神经母细胞瘤病例中表达,这表明cVE199是神经母细胞瘤治疗中潜在的抗转移治疗抗体。

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