Targeting HER3 using mono- and bispecific antibodies or alternative scaffolds

被引:37
作者
Malm, Magdalena [1 ]
Frejd, Fredrik Y. [2 ,3 ]
Stahl, Stefan [1 ]
Lofblom, John [1 ]
机构
[1] KTH Royal Inst Technol, Sch Biotechnol, Div Prot Technol, Stockholm, Sweden
[2] Affibody AB, Stockholm, Sweden
[3] Uppsala Univ, Dept Immunol Genet & Pathol, Uppsala, Sweden
关键词
Affibody molecules; alternative scaffolds; bispecific antibodies; ErbB3; HER3; monoclonal antibodies; protein therapeutics; tumor targeting; EPIDERMAL-GROWTH-FACTOR; ANTI-HER3; MONOCLONAL-ANTIBODY; C-ERBB-3 PROTEIN EXPRESSION; INHIBITS TUMOR-GROWTH; BREAST-CANCER CELLS; FACTOR RECEPTOR; TYROSINE KINASE; PHOSPHATIDYLINOSITOL; 3-KINASE; EXTRACELLULAR DOMAIN; ANTITUMOR-ACTIVITY;
D O I
10.1080/19420862.2016.1212147
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
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.
引用
收藏
页码:1195 / 1209
页数:15
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