Wu Xiaoqiong, Chen Siqi, Lin Limin, Liu Jiayu, Wang Yanlan, Li Yumei, Li Qing, Wang Zhong
School of Pharmaceutical Sciences, Sun Yat-Sen University, Guangzhou, China 510006; Center for Cellular & Structural Biology, Sun Yat-Sen University, Guangzhou, China 510006.
Transl Oncol. 2018 Apr;11(2):366-373. doi: 10.1016/j.tranon.2018.01.024. Epub 2018 Feb 20.
Human epidermal growth factor receptor 2 (HER2) is overexpressed in approximately 20% to 30% of breast cancers and various other types of cancers, which plays a vital role in the cancer progression. Monoclonal antibodies targeting Her2 are now used in the clinic to treat Her2 overexpression cancer patients. However, relapse or resistance is frequent with the current therapies. To generate a new treatment avenue against Her2, we immunized and selected a specific anti-Her2 single domain antibody C3 for further studies. The C3-Fc antibody drove antibody-dependent cell-mediated cytotoxicity against Her2-positive tumor cells in vitro and resulted in potent antitumor growth in vivo. These data suggest that the C3-Fc antibody may provide an alternative avenue for Her2-positive cancer therapy.
人表皮生长因子受体2(HER2)在约20%至30%的乳腺癌及其他多种癌症类型中过表达,其在癌症进展中起着至关重要的作用。目前临床上使用靶向Her2的单克隆抗体来治疗Her2过表达的癌症患者。然而,当前疗法中复发或耐药情况频繁出现。为了开辟针对Her2的新治疗途径,我们进行免疫并筛选出一种特异性抗Her2单域抗体C3用于进一步研究。C3-Fc抗体在体外可驱动抗体依赖性细胞介导的细胞毒性作用于Her2阳性肿瘤细胞,并在体内产生强大的抗肿瘤生长效果。这些数据表明,C3-Fc抗体可能为Her2阳性癌症治疗提供一条替代途径。