抗体-药物偶联物
结合
前列腺癌
抗体
药品
癌症
计算生物学
药物发现
癌症研究
医学
单克隆抗体
生物
免疫学
生物信息学
药理学
内科学
数学分析
数学
作者
Xiaojie Chu,Seungmin Shin,Du-San Baek,Liyong Zhang,Alex Conard,Megan Shi,Ye‐Jin Kim,Cynthia Adams,Maggie Hines,Xianglei Liu,Chuan Chen,Zehua Sun,Dontcho V. Jelev,John W. Mellors,Dimiter S. Dimitrov,Wei Li
出处
期刊:mAbs
[Landes Bioscience]
日期:2024-08-08
卷期号:16 (1)
标识
DOI:10.1080/19420862.2024.2387240
摘要
Prostate stem cell antigen (PSCA) is expressed in all stages of prostate cancer, including in advanced androgen-independent tumors and bone metastasis. PSCA may associate with prostate carcinogenesis and lineage plasticity in prostate cancer. PSCA is also a promising theranostic marker for a variety of other solid tumors, including pancreatic adenocarcinoma and renal cell carcinoma. Here, we identified a novel fully human PSCA antibody using phage display methodology. The structure-based affinity maturation yielded a high-affinity binder, F12, which is highly specific and does not bind to 6,000 human membrane proteins based on a membrane proteome array assay. F12 targets PSCA amino acids 63-69 as tested by the peptide scanning microarray, and it cross-reacts with the murine PSCA. IgG1 F12 efficiently internalizes into PSCA-expressing tumor cells. The antimitotic reagent monomethyl auristatin E (MMAE)-conjugated IgG1 F12 (ADC, F12-MMAE) exhibits dose-dependent efficacy and specificity in a human prostate cancer PC-3-PSCA xenograft NSG mouse model. This is a first reported ADC based on a fully human PSCA antibody and MMAE that is characterized in a xenograft murine model, which warrants further optimizations and investigations in additional preclinical tumor models, including prostate and other solid tumors.
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