Meng Zihan, Tan Boyu, Wang Min, Zhu Jiamin, Qu Chunrong, Cheng Zhen
Shandong First Medical University & Shandong Academy of Medical Sciences, Jinan 250117, China.
State Key Laboratory of Drug Research, Molecular Imaging Center, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai 201203, China.
ACS Med Chem Lett. 2025 Mar 26;16(4):617-624. doi: 10.1021/acsmedchemlett.5c00008. eCollection 2025 Apr 10.
TMTP1 is a tumor-homing peptide that selectively targets highly metastatic tumor cells with XPNPEP2 identified as its potential targeting receptor. Although TMTP1-based molecular probes have been explored for imaging tumors such as hepatocellular carcinoma (HCC), their clinical translation has been hampered by factors including suboptimal tumor uptake and rapid systemic clearance. To study possible solution for addressing these challenges, a cyclic TMTP1 based positron emission tomography (PET) probe, [Ga]Ga-DOTA-cTMTP1, was designed, synthesized, and evaluated for imaging HCC in small animal models. [Ga]Ga-DOTA-cTMTP1 demonstrated favorable aqueous solubility, with a log value of -3.28 ± 0.05, and it exhibited excellent in vitro stability in phosphate buffered saline (PBS) and fetal bovine serum (FBS). Biodistribution studies revealed a certain level of tumor accumulation (0.98 ± 0.14%ID/g at 30 min) and retention (0.40 ± 0.11%ID/g at 120 min). Impressively, [Ga]Ga-DOTA-cTMTP1 maintained high tumor-to-liver contrast over time, with ratios of 2.65 ± 0.45 at 30 min, 2.37 ± 0.07 at 60 min, and 2.14 ± 0.20 at 120 min. It also displayed capability of clear visualization of small HCC foci (<4 mm) in transgenic c-Myc liver tumor mice models, with tumor/liver ratios 2.20 ± 0.10 at 30 min, 2.26 ± 0.11 at 60 min, and 2.55 ± 0.44 at 120 min, respectively. Overall, this study highlights that [Ga]Ga-DOTA-cTMTP1 has favorable pharmacokinetic and in vivo tumor imaging profile, and it is a highly promising probe for visualization of HCC microlesions. Development of PET probes based on cyclic TMTP1 is a promising approach for discovering novel imaging probes.
TMTP1是一种肿瘤归巢肽,它能选择性地靶向高转移性肿瘤细胞,XPNPEP2被确定为其潜在的靶向受体。尽管已经探索了基于TMTP1的分子探针用于肝细胞癌(HCC)等肿瘤的成像,但它们的临床转化受到肿瘤摄取不理想和全身快速清除等因素的阻碍。为了研究应对这些挑战的可能解决方案,设计、合成了一种基于环化TMTP1的正电子发射断层扫描(PET)探针[Ga]Ga-DOTA-cTMTP1,并在小动物模型中对其进行了HCC成像评估。[Ga]Ga-DOTA-cTMTP1表现出良好的水溶性,log值为-3.28±0.05,并且在磷酸盐缓冲盐水(PBS)和胎牛血清(FBS)中表现出优异的体外稳定性。生物分布研究显示出一定水平的肿瘤蓄积(30分钟时为0.98±0.14%ID/g)和滞留(120分钟时为0.40±0.11%ID/g)。令人印象深刻的是,[Ga]Ga-DOTA-cTMTP1随时间保持了较高的肿瘤与肝脏对比度,30分钟时的比值为2.65±0.45,60分钟时为2.37±0.07,120分钟时为2.14±0.20。它还显示出能够在转基因c-Myc肝肿瘤小鼠模型中清晰地可视化小的HCC病灶(<4毫米),30分钟时肿瘤/肝脏比值为2.20±0.10,60分钟时为2.26±0.11,120分钟时为2.55±0.44。总体而言,这项研究突出表明[Ga]Ga-DOTA-cTMTP1具有良好的药代动力学和体内肿瘤成像特征,并且是一种用于可视化HCC微病灶的极有前景的探针。基于环化TMTP1开发PET探针是发现新型成像探针的一种有前途的方法。