EphB2 as a therapeutic antibody drug target for the treatment of colorectal cancer

被引:112
作者
Mao, WG
Luis, E
Ross, S
Silva, J
Tan, C
Crowley, C
Chui, C
Franz, G
Senter, P
Koeppen, H
Polakis, P
机构
[1] Genentech Inc, Dept Mol Biol, San Francisco, CA 94080 USA
[2] Genentech Inc, Dept Prot Chem, San Francisco, CA 94080 USA
[3] Genentech Inc, Dept Mol Oncol, San Francisco, CA 94080 USA
[4] Seattle Genet, Bothell, WA USA
关键词
D O I
10.1158/0008-5472.CAN-03-1047
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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.
引用
收藏
页码:781 / 788
页数:8
相关论文
共 46 条
[41]  
Vogt T, 1998, CLIN CANCER RES, V4, P791
[42]  
Weiner LM, 1999, SEMIN ONCOL, V26, P43
[43]  
Wilkinson DG, 2000, INT REV CYTOL, V196, P177
[44]   Multiple roles of Eph receptors and ephrins in neural development [J].
Wilkinson, DG .
NATURE REVIEWS NEUROSCIENCE, 2001, 2 (03) :155-164
[45]   Multiple signaling interactions of Abl and Arg kinases with the EphB2 receptor [J].
Yu, HH ;
Zisch, AH ;
Dodelet, VC ;
Pasquale, EB .
ONCOGENE, 2001, 20 (30) :3995-4006
[46]   Complex formation between EphB2 and Src requires phosphorylation of tyrosine 611 in the EphB2 juxtamembrane region [J].
Zisch, AH ;
Kalo, MS ;
Chong, LD ;
Pasquale, EB .
ONCOGENE, 1998, 16 (20) :2657-2670