文献类型：期刊文献

中文题名：抗EpCAM免疫毒素制备与体外活性研究

英文题名：Preparation and in vitro Activity of Anti-EpCAM Immunotoxin

作者：刘玉萍[1];邓昌平[2];马兴元[2];刘秋丽[1];鲍雯[1];郑文云[1]

机构：[1]华东理工大学药学院上海市新药设计重点实验室,上海200237;[2]华东理工大学生物工程学院生物反应器工程国家重点实验室,上海200237

年份：2023

卷号：43

期号：10

起止页码：10

中文期刊名：中国生物工程杂志

外文期刊名：China Biotechnology

收录：CSTPCD;;Scopus;北大核心:【北大核心2020】；CSCD:【CSCD2023_2024】；

基金：国家重点研发计划(2018YFA0902804)资助项目。

语种：中文

中文关键词：重组免疫毒素;EpCAM;绿脓杆菌外毒素A;单链抗体;靶向治疗

外文关键词：Recombinant immunotoxin;EpCAM;Pseudomonas aeruginosa exotoxin A;Single chain antibody;Targeted therapy

摘要：目的:上皮细胞粘附分子(epithelial cell adhesion molecule,EpCAM)在正常细胞中的表达局限于上皮基底外侧细胞,且具有隐蔽性,而在包括膀胱癌在内的多种上皮性癌症中过表达且处于易结合的状态,是抗肿瘤治疗的特异性有效靶标之一;以EpCAM作为膀胱癌靶向治疗的靶点,探索高效、安全的膀胱癌新型治疗方法。方法:在分子水平利用柔性肽GGGGS将EpCAM单链抗体4D5MOCB与毒素PE38KDEL连接设计制备免疫毒素,在大肠杆菌BL21(DE3)中进行表达,并研究其与膀胱癌细胞的结合和对癌细胞生长的抑制作用。结果:4D5MOCB介导的免疫毒素具有良好的选择性,与EpCAM高表达的膀胱癌细胞5637结合良好,其结合率约为阴性细胞结合率的169倍,并能有效抑制癌细胞生长,IC50最低可达0.5 pmol/L,同时能够抑制细胞克隆形成和细胞迁移,诱导细胞凋亡;免疫毒素与EpCAM阴性细胞HeLa不结合,也不具有抑制细胞活性的作用。结论:制备的基因工程免疫毒素具有较好的选择性,能够有效抑制阳性癌细胞的增殖和转移,且比相同抗原的抗体药物偶联物(antibody-drug conjugates,ADC)的制备更简单,均一性更好,为免疫毒素应用于实体瘤的治疗提供了实验基础。
Objective:Epithelial cell adhesion molecule(EpCAM)is one of the specific and effective targets of anti-tumor therapy,because the expression of EpCAM is limited to the basolateral epithelial cells in normal cells and is concealed.However,EpCAM is overexpressed in a variety of epithelial cancers,including bladder cancer,and is in a state of easy binding.Since immunotoxins targeting EpCAM have not been applied to the treatment of bladder cancer,new treatments for bladder cancer will be explored.Methods:The immunotoxin was constructed by linking the single-chain antibody of EpCAM 4D5MOCB with toxin PE38KDEL by flexible peptide GGGGS at the molecular level for design and preparation,and expressed in Escherichia coli BL21(DE3).The binding effect of the immunotoxin on bladder cancer cells and its inhibitory effect on the growth of bladder cancer cells were studied.Results:The quantity of 4D5MOCB-mediated immunotoxin selectively binding to positive cells is about 169 times that binding to negative cells.The immunotoxin could effectively inhibit the growth of 5637,SW780 and RT4 with an IC50 up to 0.5 pmol/L.At the same time,it could inhibit cell colony formation and cell migration and induce cell apoptosis.The immunotoxin did not bind to EpCAM-negative HeLa cells and had no inhibitory activity.Conclusion:The immunotoxin prepared in this study has good selectivity and can effectively inhibit the proliferation and metastasis of positive cancer cells.The preparation of immunotoxin is simpler than that of antibody-drug conjugates(ADCs)and it is more homogeneous than ADCs.This study also provides an experimental basis for the application of immunotoxin in the treatment of solid tumors.