{"title":"A Radiofluorinated Nanobody PET Tracer to Dynamically Visualize Differential Nectin4 Expression In Vivo.","authors":"Dongye Zheng,Yong Huang,Chengze Li,Yanye Lu,Zhaoheng Xie,Qiushi Ren,Ying Liang,Xiangxi Meng","doi":"10.1021/acs.jmedchem.5c01260","DOIUrl":null,"url":null,"abstract":"Nectin4 is a potential therapeutic target for multiple cancer types. To develop a diagnostic radiotracer for nectin4, a nanobody-based PET tracer was selected from several candidate sequences and prepared via [18F]AlF radiolabeling. The radiochemical quality was assessed, and tracer uptake was evaluated in cell lines and tumor models with varying nectin4 expression levels. In vitro and in vivo studies showed that the tracer exhibited a specific affinity for nectin4, with a binding affinity (KD) of 6.77 nM in cell lines. The tracer enabled clear visualization of nectin4-expressing lesions, and its uptake profile and pharmacokinetic behavior were characterized using dynamic PET imaging and kinetic analysis. A correlation between PET signal intensity and histological nectin4 expression was also observed in tumor models. Thus, it may have the potential to become a nectin4 tracer for clinical applications.","PeriodicalId":46,"journal":{"name":"Journal of Medicinal Chemistry","volume":"6 1","pages":""},"PeriodicalIF":6.8000,"publicationDate":"2025-10-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Medicinal Chemistry","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1021/acs.jmedchem.5c01260","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MEDICINAL","Score":null,"Total":0}
引用次数: 0
Abstract
Nectin4 is a potential therapeutic target for multiple cancer types. To develop a diagnostic radiotracer for nectin4, a nanobody-based PET tracer was selected from several candidate sequences and prepared via [18F]AlF radiolabeling. The radiochemical quality was assessed, and tracer uptake was evaluated in cell lines and tumor models with varying nectin4 expression levels. In vitro and in vivo studies showed that the tracer exhibited a specific affinity for nectin4, with a binding affinity (KD) of 6.77 nM in cell lines. The tracer enabled clear visualization of nectin4-expressing lesions, and its uptake profile and pharmacokinetic behavior were characterized using dynamic PET imaging and kinetic analysis. A correlation between PET signal intensity and histological nectin4 expression was also observed in tumor models. Thus, it may have the potential to become a nectin4 tracer for clinical applications.
期刊介绍:
The Journal of Medicinal Chemistry is a prestigious biweekly peer-reviewed publication that focuses on the multifaceted field of medicinal chemistry. Since its inception in 1959 as the Journal of Medicinal and Pharmaceutical Chemistry, it has evolved to become a cornerstone in the dissemination of research findings related to the design, synthesis, and development of therapeutic agents.
The Journal of Medicinal Chemistry is recognized for its significant impact in the scientific community, as evidenced by its 2022 impact factor of 7.3. This metric reflects the journal's influence and the importance of its content in shaping the future of drug discovery and development. The journal serves as a vital resource for chemists, pharmacologists, and other researchers interested in the molecular mechanisms of drug action and the optimization of therapeutic compounds.