Pharmaceutical Research Division, Takeda Pharmaceutical Company Limited, 26-1, Muraokahigashi 2-chome, Fujisawa, Kanagawa 251-8555, Japan.
Mol Cancer. 2013 Jun 12;12:60. doi: 10.1186/1476-4598-12-60.
Nectin-2 is a Ca(2+)-independent cell-cell adhesion molecule that is one of the plasma membrane components of adherens junctions. However, little has been reported about the involvement of Nectin-2 in cancer.
To determine the expression of Nectin-2 in cancer tissues and cancer cell lines, we performed gene expression profile analysis, immunohistochemistry studies, and flow cytometry analysis. We also investigated the potential of this molecule as a target for antibody therapeutics to treat cancers by generating and characterizing an anti-Nectin-2 rabbit polyclonal antibody (poAb) and 256 fully human anti-Nectin-2 monoclonal antibodies (mAbs). In addition, we tested anti-Nectin-2 mAbs in several in vivo tumor growth inhibition models to investigate the primary mechanisms of action of the mAbs.
In the present study, we found that Nectin-2 was over-expressed in clinical breast and ovarian cancer tissues by using gene expression profile analysis and immunohistochemistry studies. Nectin-2 was over-expressed in various cancer cell lines as well. Furthermore, the polyclonal antibody specific to Nectin-2 suppressed the in vitro proliferation of OV-90 ovarian cancer cells, which express endogenous Nectin-2 on the cell surface. The anti-Nectin-2 mAbs we generated were classified into 7 epitope bins. The anti-Nectin-2 mAbs demonstrated antibody-dependent cellular cytotoxicity (ADCC) and epitope bin-dependent features such as the inhibition of Nectin-2-Nectin-2 interaction, Nectin-2-Nectin-3 interaction, and in vitro cancer cell proliferation. A representative anti-Nectin-2 mAb in epitope bin VII, Y-443, showed anti-tumor effects against OV-90 cells and MDA-MB-231 breast cancer cells in mouse therapeutic models, and its main mechanism of action appeared to be ADCC.
We observed the over-expression of Nectin-2 in breast and ovarian cancers and anti-tumor activity of anti-Nectin-2 mAbs via strong ADCC. These findings suggest that Nectin-2 is a potential target for antibody therapy against breast and ovarian cancers.
Nectin-2 是一种不依赖 Ca(2+)的细胞间黏附分子,是黏着连接的质膜组成部分之一。然而,关于 Nectin-2 在癌症中的作用,目前报道较少。
为了确定 Nectin-2 在癌症组织和癌细胞系中的表达,我们进行了基因表达谱分析、免疫组织化学研究和流式细胞术分析。我们还通过生成和表征针对 Nectin-2 的抗兔多克隆抗体(poAb)和 256 种完全人源抗 Nectin-2 单克隆抗体(mAb),研究了该分子作为治疗癌症的抗体治疗靶标的潜力。此外,我们在几种体内肿瘤生长抑制模型中测试了抗 Nectin-2 mAb,以研究 mAb 的主要作用机制。
在本研究中,我们通过基因表达谱分析和免疫组织化学研究发现,Nectin-2 在临床乳腺癌和卵巢癌组织中过表达。各种癌细胞系也过表达 Nectin-2。此外,针对 Nectin-2 的多克隆抗体特异性抑制了表达内源性 Nectin-2 的 OV-90 卵巢癌细胞的体外增殖。我们生成的抗 Nectin-2 mAb 被分为 7 个表位簇。抗 Nectin-2 mAb 表现出抗体依赖的细胞毒性(ADCC)和表位簇依赖性特征,如抑制 Nectin-2-Nectin-2 相互作用、Nectin-2-Nectin-3 相互作用以及体外癌细胞增殖。表位簇 VII 中的代表性抗 Nectin-2 mAb Y-443 在小鼠治疗模型中对 OV-90 细胞和 MDA-MB-231 乳腺癌细胞表现出抗肿瘤作用,其主要作用机制似乎是 ADCC。
我们观察到 Nectin-2 在乳腺癌和卵巢癌中的过表达以及抗 Nectin-2 mAb 的抗肿瘤活性,通过强大的 ADCC。这些发现表明 Nectin-2 是针对乳腺癌和卵巢癌的抗体治疗的潜在靶标。