Liao Mei-Ying, Lai Jun-Kai, Kuo Mark Yen-Ping, Lu Ruei-Min, Lin Cheng-Wei, Cheng Ping-Chang, Liang Kang-Hao, Wu Han-Chung
Institute of Cellular and Organismic Biology, Academia Sinica, Taipei, Taiwan.
Graduate Institute of Clinical Dentistry, School of Dentistry, National Taiwan University, Taipei, Taiwan.
Oncotarget. 2015 Sep 22;6(28):24947-68. doi: 10.18632/oncotarget.4453.
Epithelial cell adhesion molecule (EpCAM) is known to be overexpressed in epithelial cancers associated with enhanced malignant potential, particularly colorectal carcinoma (CRC) and head and neck squamous cell carcinoma (HNSCC). However, it is unknown whether progression of malignance can be directly inhibited by targeting EpCAM. Here, we have generated five novel monoclonal antibodies (mAbs) against EpCAM. One of these anti-EpCAM mAbs, EpAb2-6, was found to induce cancer cell apoptosis in vitro, inhibit tumor growth, and prolong the overall survival of both a pancreatic cancer metastatic mouse model and mice with human colon carcinoma xenografts. EpAb2-6 also increases the therapeutic efficacy of irinotecan, fluorouracil, and leucovorin (IFL) therapy in a colon cancer animal model and gemcitabine therapy in a pancreatic cancer animal model. Furthermore, EpAb2-6, which binds to positions Y95 and D96 of the EGF-II/TY domain of EpCAM, inhibits production of EpICD, thereby decreasing its translocation and subsequent signal activation. Collectively, our results indicate that the novel anti-EpCAM mAb can potentially be used for cancer-targeted therapy.
上皮细胞粘附分子(EpCAM)在与恶性潜能增强相关的上皮癌中过度表达,尤其是在结直肠癌(CRC)和头颈部鳞状细胞癌(HNSCC)中。然而,靶向EpCAM是否能直接抑制恶性肿瘤进展尚不清楚。在此,我们制备了五种新型抗EpCAM单克隆抗体(mAb)。其中一种抗EpCAM mAb,即EpAb2-6,被发现可在体外诱导癌细胞凋亡,抑制肿瘤生长,并延长胰腺癌转移小鼠模型和人结肠癌异种移植小鼠的总生存期。EpAb2-6还可提高伊立替康、氟尿嘧啶和亚叶酸(IFL)疗法在结肠癌动物模型中的治疗效果,以及吉西他滨疗法在胰腺癌动物模型中的治疗效果。此外,与EpCAM的EGF-II/TY结构域的Y95和D96位点结合的EpAb2-6可抑制EpICD的产生,从而减少其易位及随后的信号激活。总体而言,我们的结果表明,这种新型抗EpCAM mAb有潜力用于癌症靶向治疗。