Mao Weiguang, Luis Elizabeth, Ross Sarajane, Silva Johnny, Tan Christine, Crowley Craig, Chui Clarissa, Franz Gretchen, Senter Peter, Koeppen Hartmut, Polakis Paul
Department of Molecular Biology, Genentech, Inc., South San Francisco, California, USA.
Cancer Res. 2004 Feb 1;64(3):781-8. doi: 10.1158/0008-5472.can-03-1047.
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.
对人类结肠直肠癌标本的分析显示EphB2受体酪氨酸激酶过表达。制备了针对EphB2细胞外序列的单克隆抗体(MAb),并测试其对结肠直肠癌细胞的活性。其中一种单克隆抗体2H9有效地阻断了EphB2与ephrin配体的相互作用,并抑制了受体随后的自磷酸化。然而,该抗体不影响表达EphB2的癌细胞的增殖。免疫细胞化学分析显示,单克隆抗体2H9与EphB2结合后迅速内化,这表明通过抗体-药物偶联物可以实现靶向依赖性细胞杀伤。当单克隆抗体2H9通过组织蛋白酶B可裂解的连接子与单甲基澳瑞他汀E偶联时,它在体外和体内特异性杀死表达EphB2的癌细胞。我们的结果表明,EphB2是免疫缀合物癌症治疗的一个有吸引力的靶点。