化学
肺癌
癌症研究
免疫组织化学
抗体
跨膜蛋白
癌症
单克隆抗体
拉顿
正电子发射断层摄影术
癌
肺
病理
肿瘤细胞
癌症治疗
细胞培养
分子生物学
癌细胞
Pet成像
体内
下调和上调
蛋白质表达
特异性抗体
分子探针
作者
Guanyun Wang,Lingling Zheng,Xu Yang,Xiaoya Wang,Zi’ang Zhou,Ying Kan,Wei Wang,Jianhua Gong,Jigang Yang
标识
DOI:10.1021/acs.jmedchem.5c02806
摘要
Seizure-related 6 homologue (SEZ6) is a highly expressed transmembrane protein that has emerged as a promising therapeutic target for small-cell lung cancer (SCLC). In this study, we developed a novel immuno-positron emission tomography probe ([64Cu]Cu-NOTA-GGB02-F9) based on the SEZ6-targeting antibody, GGB02-F9, for use in preclinical mouse models of SCLC. The diagnostic potential of [64Cu]Cu-NOTA-GGB02-F9 was evaluated in preclinical SCLC models with varying levels of SEZ6 expression. The H69 tumors exhibited a distinct accumulation of tracer uptake in the tumor xenograft mice, reaching a maximum uptake at 72 h postinjection, which was significantly higher than that in the H69 GGB02-F9-blocked and H460 groups (P < 0.01) at 24, 48, and 72 h postinjection. The uptake of the tumor tracer in mice was found to be associated with SEZ6 expression, as determined by immunohistochemical analysis. Our study demonstrated that [64Cu]Cu-NOTA-GGB02-F9 can noninvasively evaluate SEZ6 expression in preclinical SCLC mouse models.
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