放射合成
胰腺癌
化学
正电子发射断层摄影术
癌症研究
Pet成像
胰腺导管腺癌
结合
分子成像
腺癌
胰腺
胰腺肿瘤
仿形(计算机编程)
显像剂
癌症
肿瘤微环境
基因表达谱
胰腺疾病
临床前影像学
示踪剂
吉西他滨
癌细胞
细胞培养
光学成像
分子探针
肿瘤细胞
病理
比活度
作者
Tingting Wang,Jingchao Li,Xiangping Chen,Xiangping Chen,Xun zhang,Dongsheng Zhang,Guangfa Wang,Jian‐Mei Li,Yafei Zhang,Nian Liu,Xiao Chen,Xiao Chen,Xinhui Su
标识
DOI:10.1021/acs.jmedchem.5c02777
摘要
Pancreatic ductal adenocarcinoma (PDAC) remains challenging to diagnose in its early stages. Capitalizing on the established overexpression of plectin-1 in PDAC, we developed a novel plectin-1-targeted positron emission tomography (PET) radiotracer, [68Ga]Ga-NOTA-PTP, for precise PDAC imaging. The NOTA-PTP conjugate was synthesized, characterized, and efficiently radiolabeled with 68Ga, achieving high radiochemical purity (>99%). The radiotracer displayed a strong binding affinity for plectin-1 (IC50 = 12.8 nM) and exhibited time-dependent accumulation in PDAC cells. In murine PDAC xenografts, PET imaging demonstrated the rapid and specific tumor uptake of [68Ga]Ga-NOTA-PTP, enabling the visualization of peritoneal metastases. Targeting specificity was further verified by both the significant reduction in tumor uptake upon preadministration of the unlabeled compound and the positive correlation between tracer accumulation and plectin-1 expression levels. Collectively, this work introduces the first plectin-1-targeted PET probe for specific and sensitive detection of PDAC and metastatic lesions through efficient plectin-1 engagement.
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