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ANTITUMOR EFFECT OF AN ANTI-ENDOTHELIAL CELL MONOCLONAL ANTIBODY BVE-1 ON SOLID TUMOR XENOGRAFT IN NUDE MICE

  
@article{CJCR1632,
	author = {Peiyu Li and Mei Yuan and Hongtian Xia and li Li and Yongxin Fang and Lihua Fei and Yanyong Jiang and Xiyun Yan},
	title = {ANTITUMOR EFFECT OF AN ANTI-ENDOTHELIAL CELL MONOCLONAL ANTIBODY BVE-1 ON SOLID TUMOR XENOGRAFT IN NUDE MICE},
	journal = {Chinese Journal of Cancer Research},
	volume = {11},
	number = {2},
	year = {2013},
	keywords = {},
	abstract = {Objective: To study the possibility of treatment for solid tumors by targeting vascular endothelial cells with a monoclonal antibody (MoAb) BVE-1. 
Methods: Leiomyosarcoma cell line SK-LMS-1, liver cancer cell line 7721 and pancreatic cancer cell line SW1990 xenografts in nude mice were treated ip with an antiendothelial cell monoclonal antibody BVE-1 or a31I labeled BVE-I, with normal mouse IgG or 131 I labeled IgG as controls. The tumor volume was measured at regular intervals following treatment. After sacrificing of the mice, the tumors were histologically examined and the intra-tumoral microvesse| density (TMVD) recorded. 
Results: The inhibition effects of tumor growth in mice treated with BVE-1 were 49.8% in SKLMS- 1, 48.7% in SW1990 and 70.5 in 7721 respectively. Metastasis of leiomyosarcoma was also inhibited by the antibody treatment, leading to a decrease in the death rate. This effect was enhanced when treated with 131Ilabeled BVE-1 as the inhibition rate of tumor growth increased to 82.2-86.6 %. Pathologically, vascular endothelial cells degeneration, occlusion of blood vessels and massive tumor cells necrosis around the degenerated vessels were observed in the BVE-1 treated mice. TMVD was significantly lower in the BVE-1 treated mice than that in mice treated with normal mouse IgG and in the untreated mice. 
Conclusion: The monoclonal antibody against vascular endothelial cells BVE-1 is effective in the treatment of human cancer xeno-grafted in nude mice by the induction of vascular endothelial degeneration and vascular occlusion inside the tumor. It may be used as a novel strategic approach in the treatment of human solid tumors.},
	issn = {1993-0631},	url = {https://cjcr.amegroups.org/article/view/1632}
}