An antibody directed against PDGF receptor β enhances the antitumor and the anti-angiogenic activities of an anti-VEGF receptor 2 antibody

被引:36
|
作者
Shen, Juqun [1 ]
Vil, Marie D. [1 ]
Zhang, Haifan [1 ]
Tonra, James R. [1 ]
Rong, Ling L. [1 ]
Damoci, Chris [1 ]
Prewett, Marie [1 ]
Deevi, Dhanvanthri S. [1 ]
Kearney, Jessica [1 ]
Surguladze, David [1 ]
Jimenez, Xenia [1 ]
Iacolina, Michelle [1 ]
Bassi, Rajiv [1 ]
Zhou, Kai [1 ]
Balderes, Paul [1 ]
Mangalampalli, Venkat R. M. [1 ]
Loizos, Nick [1 ]
Ludwig, Dale L. [1 ]
Zhu, Zhenping [1 ]
机构
[1] ImClone Syst Inc, New York, NY 10014 USA
关键词
angiogenesis; pericyte; endothelial cells; PDGFR; VEGFR2; neutralizing antibody; antibody combination; cancer therapy;
D O I
10.1016/j.bbrc.2007.04.075
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Platelet-derived growth factor (PDGF) and its receptors (PDGFR) play important roles in tumorigenesis through stimulating tumor growth and promoting angiogenesis via enhancing pericyte recruitment and vessel maturation. Here we produced a neutralizing antibody, IB3, directed against mouse PDGFR beta. IB3 binds to PDGFR beta with high affinity (9 x 10(-11) M) and blocks PDGF-BB from binding to the receptor with an IC50 of similar to 1.2 nM. The antibody also blocks ligand-stimulated activation of PDGFR beta and downstream signaling molecules, including Akt and MAPK p42/44, in tumor cells. In animal studies, IB3 significantly enhanced the antitumor and the anti-angiogenic activities of DC101, an antibody directed against mouse vascular endothelial growth factor receptor 2, in a pancreatic (BxPC-3) and a non-small cell lung (NCI-H460) tumor xenograft models. Treatment with the combination of IB3 and DC101 in BxPC-3 xenograft-bearing mice resulted in tumor regression in 58% of mice compared to that in 18% of mice treated with DC101 alone. Taken together, these results lend great support to use PDGFR beta antagonists in combinations with other antitumor and/or anti-angiogenic agents in the treatment of a variety of cancers. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:1142 / 1147
页数:6
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