Targeting Human Epidermal Growth Factor Receptor Signaling with the Neuregulin's Heparin-binding Domain

被引:21
|
作者
Ma, Zhenzhong
Li, Qunfang
An, Haiqian [1 ]
Pankonin, Mark S.
Wang, Jiajing
Loeb, Jeffrey A. [1 ]
机构
[1] Wayne State Univ, Sch Med, Dept Neurol, Detroit, MI 48201 USA
关键词
METASTATIC BREAST-CANCER; EPITHELIAL-CELLS; NERVOUS-SYSTEM; IN-VIVO; HEREGULIN; TUMORIGENICITY; ANTIBODY; FORMS; ARIA; HER2;
D O I
10.1074/jbc.M109.032714
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
A major limitation in biopharmaceutical development is selectively targeting drugs to diseased tissues. Growth factors and viruses have solved this problem by targeting tissue-specific cell-surface heparan sulfates. Neuregulin (NRG), a growth factor important in both nervous system development and cancer, has a unique heparin-binding domain (HBD) that targets to cell surfaces expressing its HER2/3/4 receptors (Esper, R. M., Pankonin, M. S., and Loeb, J. A. (2006) Brain Res. Rev. 51, 161-175). We have harnessed this natural targeting ability of NRG by fusing the HBD of NRG to soluble HER4. This fusion protein retains high affinity heparin binding to heparin and to cells that express heparan sulfates resulting in a more potent NRG antagonist. In vivo, it is targeted to peripheral nerve segments where it blocks the activity of NRG as a Schwann cell survival factor. The fusion protein also efficiently blocks autocrine and paracrine signaling and reduces the proliferation of MCF10CA1 breast cancer cells. These findings demonstrate the utility of the HBD of NRG in biopharmaceutical targeting and provide a new way to block HER signaling in cancer cells.
引用
收藏
页码:32108 / 32115
页数:8
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