Structure-based approaches to inhibition of erbB receptors with peptide mimetics

被引:4
|
作者
Berezov, A
Greene, MI
Murali, R
机构
[1] Univ Penn, Sch Med, Dept Pathol & Lab Med, Philadelphia, PA 19104 USA
[2] Abramson Family Canc Res Inst, Philadelphia, PA USA
关键词
antibodies; inhibitors; HER2; disabling erbB receptor ensembles; structure-based design; peptidomimetics;
D O I
10.1385/IR:27:2-3:303
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The epidermal growth factor (EGF) family of tyrosine kinase receptors (erbB receptors) are expressed at high levels in a wide variety of human cancers and have been associated with various features of advanced disease and poor prognosis. Therapeutic blockade of erbB signaling is a novel approach to the treatment of human tumors that could offer a noncytotoxic alternative to cancer treatment. A number of monoclonal antibodies (MAbs) directed against erbB receptors have been developed and demonstrated promising therapeutic results. We have designed small-molecule peptide mimetics of an anti-erbB rhu MAb 4D5 that can mimic structural and functional properties of the parental antibody. An alternative structure-based strategy of erbB receptor blockade with peptide milnetics by targeting receptor dimerization interfaces is also described.
引用
收藏
页码:303 / 308
页数:6
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