肝细胞癌
体内分布
化学
肽
分子探针
生物标志物
癌症研究
分子成像
小分子
肝癌
免疫组织化学
病理
肿瘤细胞
环肽
寡肽
癌症
光学成像
精确肿瘤学
分子生物学
癌
肝肿瘤
诊断生物标志物
作者
Chen Gong,Gangzhong Zhou,Xudong Sun,Zhencun Cui,Hange Yang,Cong Wang,Kun Wang,Xuegong Fan,Peihong Ji,Ke Wang,Jianshan Liu,Jianshan Liu,Yuhao He,Hui Wang,Hongyan Li,Yimeng Zhu,Zhimin Wang,Kuan Hu,Jiangyan Liu,Jiangyan Liu
标识
DOI:10.1021/acs.jmedchem.5c02081
摘要
Hepatocellular carcinoma (HCC) remains a growing global health threat, necessitating the development of precise molecular probes for its prevention, early diagnosis, and treatment. Glypican-3 (GPC3) is highly expressed in various HCC subtypes and exhibits minimal expression in normal liver tissue, making it a promising biomarker for early-stage HCC diagnosis. Herein, we report a novel cyclic peptide molecular probe, 10P3Me, exhibiting high binding affinity for GPC3, with a K d of 93.8 nM. In PET-imaging studies, 10P3Me showed pronounced tumor-targeting ability in GPC3-positive models, reaching a peak uptake of 5.61%ID/mL at 1 h post-injection, 3.8-fold higher than in GPC3-low models. 10P3Me also displayed robust targeting in an orthotopic HepG2-LUC liver tumor model, enabling accurate localization of intrahepatic lesions. Biodistribution revealed selective tumor accumulation over normal liver, achieving a tumor-to-liver uptake ratio of 8.28 at 1 h. These findings highlight 10P3Me as a promising probe for molecular imaging of GPC3-positive HCC.
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