EV20, a Novel Anti-ErbB-3 Humanized Antibody, Promotes ErbB-3 Down-Regulation and Inhibits Tumor Growth In Vivo

被引:31
|
作者
Sala, Gianluca [1 ,2 ]
Rapposelli, Ilario Giovanni [2 ]
Ghasemi, Reza [2 ,3 ]
Piccolo, Enza [1 ,2 ]
Traini, Sara [1 ,2 ]
Capone, Emily [2 ]
Rossi, Cosmo [2 ]
Pelliccia, Angela [4 ]
Di Risio, Annalisa [1 ,2 ]
D'Egidio, Maurizia [2 ]
Tinari, Nicola [1 ,2 ]
Muraro, Raffaella [1 ,2 ]
Iacobelli, Stefano [1 ,2 ]
机构
[1] MediaPharma Srl, Chieti, Italy
[2] Univ G dAnnunzio, Dept Expt & Clin Sci, I-66100 Chieti, Italy
[3] Tehran Univ Med Sci, Sch Med, Dept Med Genet, Tehran, Iran
[4] Sigma Tau Ind Farmaceut Riunite SpA, Pomezia, Italy
来源
TRANSLATIONAL ONCOLOGY | 2013年 / 6卷 / 06期
关键词
D O I
10.1593/tlo.13475
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
ErbB-3 (HER-3) receptor is involved in tumor progression and resistance to therapy. Development of specific inhibitors impairing the activity of ErbB-3 is an attractive tool for cancer therapeutics. MP-RM-1, a murine monoclonal antibody targeting human ErbB-3, has shown anticancer activity in preclinical models. With the aim to provide novel candidates for clinical use, we have successfully generated a humanized version of MP-RM-1. The humanized antibody, named EV20, abrogates both ligand-dependent and ligand-independent receptor signaling of several tumor cell types, strongly promotes ErbB-3 down-regulation, and efficiently and rapidly internalizes into tumor cells. Furthermore, treatment with EV20 significantly inhibits growth of xenografts originating from prostatic, ovarian, and pancreatic cancers as well as melanoma in nude mice. In conclusion, we provide a novel candidate for ErbB-3-targeted cancer therapy.
引用
收藏
页码:676 / U293
页数:11
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