Division of Molecular Imaging, Department of Medicinal Chemistry, Uppsala University, Uppsala, Sweden.
PET & Cyclotron Unit, Department of Nuclear Medicine, Odense University Hospital, Odense, Denmark.
Contrast Media Mol Imaging. 2017 Aug 10;2017:6873684. doi: 10.1155/2017/6873684. eCollection 2017.
High gastrin releasing peptide receptor (GRPR) expression is associated with numerous cancers including prostate and breast cancer. The aim of the current study was to develop a Co-labeled PET agent based on GRPR antagonist RM26 for visualization of GRPR-expressing tumors. Labeling with Co and Co, stability, binding specificity, and in vitro and in vivo characteristics of Co-NOTA-PEG-RM26 were studied. NOTA-PEG-RM26 was successfully radiolabeled with Co and Co with high yields and demonstrated high stability. The radiopeptide showed retained binding specificity to GRPR in vitro and in vivo. Co-NOTA-PEG-RM26 biodistribution in mice was characterized by rapid clearance of radioactivity from blood and normal non-GRPR-expressing organs and low hepatic uptake. The clearance was predominantly renal with a low degree of radioactivity reabsorption. Tumor-to-blood ratios were approximately 200 (3 h pi) and 1000 (24 h pi). The favorable biodistribution of cobalt-labeled NOTA-PEG-RM26 translated into high contrast preclinical PET/CT (using Co) and SPECT/CT (using Co) images of PC-3 xenografts. The initial biological results suggest that Co-NOTA-PEG-RM26 is a promising tracer for PET visualization of GRPR-expressing tumors.
高胃泌素释放肽受体 (GRPR) 的表达与许多癌症有关,包括前列腺癌和乳腺癌。本研究的目的是开发一种基于 GRPR 拮抗剂 RM26 的共标记 PET 试剂,用于可视化表达 GRPR 的肿瘤。研究了 Co 和 Co 标记、稳定性、结合特异性以及 Co-NOTA-PEG-RM26 的体外和体内特性。NOTA-PEG-RM26 成功地用 Co 和 Co 进行了放射性标记,具有高产率和高稳定性。放射性肽在体外和体内均表现出保留的 GRPR 结合特异性。Co-NOTA-PEG-RM26 在小鼠中的生物分布特征是放射性从血液和正常非 GRPR 表达器官中的快速清除以及肝脏摄取低。清除主要通过肾脏进行,放射性再吸收程度低。肿瘤与血液的比值约为 200(3 h pi)和 1000(24 h pi)。钴标记的 NOTA-PEG-RM26 的良好生物分布转化为 GRPR 表达肿瘤的高对比度临床前 PET/CT(使用 Co)和 SPECT/CT(使用 Co)图像。初步的生物学结果表明,Co-NOTA-PEG-RM26 是一种有前途的用于 GRPR 表达肿瘤 PET 可视化的示踪剂。