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使用单特异性和双特异性抗体或其他支架靶向HER3。

Targeting HER3 using mono- and bispecific antibodies or alternative scaffolds.

作者信息

Malm Magdalena, Frejd Fredrik Y, Ståhl Stefan, Löfblom John

机构信息

a Division of Protein Technology, School of Biotechnology, KTH-Royal Institute of Technology, SE , Stockholm.

b Affibody AB, SE, Stockholm , Sweden.

出版信息

MAbs. 2016 Oct;8(7):1195-1209. doi: 10.1080/19420862.2016.1212147. Epub 2016 Aug 17.

Abstract

The human epidermal growth factor receptor 3 (HER3) has in recent years been recognized as a key node in the complex signaling network of many different cancers. It is implicated in de novo and acquired resistance against therapies targeting other growth factor receptors, e.g., EGFR, HER2, and it is a major activator of the PI3K/Akt signaling pathway. Consequently, HER3 has attracted substantial attention, and is today a key target for drugs in clinical development. Sophisticated protein engineering approaches have enabled the generation of a range of different affinity proteins targeting this receptor, including antibodies and alternative scaffolds that are either mono- or bispecific. Here, we describe HER3 and its role as a key tumor target, and give a comprehensive review of HER3-targeted proteins currently in development, including discussions on the opportunities and challenges of targeting this receptor.

摘要

近年来,人类表皮生长因子受体3(HER3)已被公认为多种不同癌症复杂信号网络中的关键节点。它与针对其他生长因子受体(如EGFR、HER2)的治疗的原发性和获得性耐药有关,并且是PI3K/Akt信号通路的主要激活剂。因此,HER3引起了广泛关注,如今是临床开发中药物的关键靶点。先进的蛋白质工程方法已能够生成一系列针对该受体的不同亲和蛋白,包括单特异性或双特异性的抗体和替代支架。在这里,我们描述HER3及其作为关键肿瘤靶点的作用,并对目前正在开发的HER3靶向蛋白进行全面综述,包括对靶向该受体的机遇和挑战的讨论。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e0f/5058629/053c4d339efa/kmab-08-07-1212147-g001.jpg

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