| Literature DB >> 14871799 |
Weiguang Mao1, Elizabeth Luis, Sarajane Ross, Johnny Silva, Christine Tan, Craig Crowley, Clarissa Chui, Gretchen Franz, Peter Senter, Hartmut Koeppen, Paul Polakis.
Abstract
Analysis of human colorectal cancer specimens revealed overexpression of the EphB2 receptor tyrosine kinase. Monoclonal antibodies (MAbs) to extracellular sequence of EphB2 were raised and tested for activity against colorectal cancer cells. One of the MAbs, 2H9, effectively blocked the interaction of ephB2 with ephrin ligands and inhibited the resulting autophosphorylation of the receptor. However, this antibody did not affect the proliferation of cancer cells expressing ephB2. Immunocytochemical analysis revealed rapid internalization of the MAb 2H9 on binding ephB2, suggesting that target-dependent cell killing could be achieved with an antibody-drug conjugate. When MAb 2H9 was conjugated to monomethylauristatin E through a cathepsin B-cleavable linker, it specifically killed ephB2-expressing cancer cells in vitro and in vivo. Our results suggest that ephB2 is an attractive target for immunoconjugate cancer therapy.Entities:
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Year: 2004 PMID: 14871799 DOI: 10.1158/0008-5472.can-03-1047
Source DB: PubMed Journal: Cancer Res ISSN: 0008-5472 Impact factor: 12.701