首页> 美国卫生研究院文献>Translational Oncology >EV20 a Novel Anti-ErbB-3 Humanized Antibody Promotes ErbB-3 Down-Regulation and Inhibits Tumor Growth In Vivo
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EV20 a Novel Anti-ErbB-3 Humanized Antibody Promotes ErbB-3 Down-Regulation and Inhibits Tumor Growth In Vivo

机译:EV20一种新型抗ErbB-3人源化抗体可促进ErbB-3下调并抑制体内肿瘤的生长

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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.
机译:ErbB-3(HER-3)受体参与肿瘤的进展和对治疗的抵抗力。破坏ErbB-3活性的特异性抑制剂的开发是用于癌症治疗的有吸引力的工具。 MP-RM-1是一种针对人ErbB-3的鼠类单克隆抗体,已在临床前模型中显示出抗癌活性。为了为临床提供新颖的候选药物,我们成功生成了人性化的MP-RM-1。被称为EV20的人源化抗体消除了几种肿瘤细胞类型的配体依赖性和配体依赖性受体信号,强烈促进ErbB-3下调,并有效且快速地内化到肿瘤细胞中。此外,在裸鼠中,用EV20处理可显着抑制源自前列腺癌,卵巢癌和胰腺癌以及黑色素瘤的异种移植物的生长。总之,我们为针对ErbB-3的癌症治疗提供了一种新的候选药物。

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