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用于前列腺癌诊断和手术导航的PSMA靶向荧光和PET成像示踪剂[镓]镓-NYM036的临床前研究

Preclinical Study of the PSMA-Targeting Fluorescent and PET Imaging Tracer [Ga]Ga-NYM036 for Prostate Cancer Diagnosis and Surgical Navigation.

作者信息

Zhang Yu, Yan Chenglong, Yu Shanyou, Yu Chunjing, Chen Liping

机构信息

Department of Nuclear Medicine, Affiliated Hospital of Jiangnan University, Wuxi 214062, P. R. China.

Norroybiopharm Co., Ltd., Wuxi 214122, P. R. China.

出版信息

Mol Pharm. 2025 Sep 12. doi: 10.1021/acs.molpharmaceut.5c01019.

DOI:10.1021/acs.molpharmaceut.5c01019
PMID:40938807
Abstract

Prostate-specific membrane antigen (PSMA) is a biomarker and molecular imaging target with the potential for the development and application of theranostic radiopharmaceuticals. Our study designed and developed PSMA-targeted small-molecule structures with diagnostic and therapeutic significance and screened out a precursor molecular structure NYM036 with PET diagnostic and fluorescence imaging potential and mainly explored the PET imaging biodistribution and fluorescence imaging of [Ga]Ga-NYM036 in prostate cancer model mice. After design and optimization, a small-molecule structure (named NYM036) characterized with fluorescence imaging and radionuclide-labeling functions was obtained. In the LNcaP prostate cancer mouse model, the preclinical targeted imaging efficacy and biodistribution of [Ga]Ga-NYM036 were studied using microPET/CT imaging. The feasibility of using the fluorescence imaging function of [Ga]Ga-NYM036 for tumor boundary differentiation and surgical navigation was verified through live fluorescence imaging and simulation of the surgical resection of prostate cancer. MicroPET/CT imaging in LNcaP tumor-bearing mice showed that [Ga]Ga-NYM036 had quite a low accumulation in nontarget organs (except for kidneys) and a high uptake in tumors. Blocked with 10-fold of the mass dose of NYM036, the radioactive uptake in tumors decreased significantly (%ID/g-mean, from 20.91 ± 3.11 to 4.12 ± 0.54, < 0.001), with the tumor-to-muscle ratio decreased from 16.85 ± 5.09 to 3.57 ± 0.66, but the radiouptakes in other organs had no obvious change. [Ga]Ga-NYM036 had a high and fast biodistribution in tumors, and the high target uptake lasted at least for 3 h after injection (%ID/g-mean value: 1 h, 22.05 ± 3.72; 3 h, 25.11 ± 4.87). The acute toxicity experiments conducted in ICR mice showed the good safety of [Ga]Ga-NYM036. Fluorescence imaging and tumor resection surgery with [Ga]Ga-NYM036 in LNcaP tumor-bearing mice displayed that the nuclide-labeled PSMA-targeting radiotracer [Ga]Ga-NYM036, which was coupled via a covalent bond with the Cy7 fluorescent dye, has a significant imaging effect and a good surgical navigation function for tumor tissues in the LNcaP prostate cancer mouse model. The PET imaging analysis results of radioactive uptakes for tumors and multiple organ tissues showed that [Ga]Ga-NYM036 has a good targeting capability for tumors, a low uptake in nontarget organs, and a good PET imaging efficiency in prostate cancer models. [Ga]Ga-NYM036 PET imaging may be applied to diagnosis and preoperative planning, and its fluorescence imaging function can be used in intraoperative navigation and postoperative efficacy evaluation, helping to achieve precise clearance surgery and subsequent treatment of prostate cancer.

摘要

前列腺特异性膜抗原(PSMA)是一种生物标志物和分子成像靶点,具有开发和应用治疗诊断放射性药物的潜力。我们的研究设计并开发了具有诊断和治疗意义的PSMA靶向小分子结构,筛选出具有PET诊断和荧光成像潜力的前体分子结构NYM036,并主要探索了[镓]Ga-NYM036在前列腺癌模型小鼠中的PET成像生物分布和荧光成像。经过设计和优化,获得了具有荧光成像和放射性核素标记功能的小分子结构(命名为NYM036)。在LNcaP前列腺癌小鼠模型中,使用微型PET/CT成像研究了[镓]Ga-NYM036的临床前靶向成像效果和生物分布。通过活体荧光成像和前列腺癌手术切除模拟,验证了[镓]Ga-NYM036的荧光成像功能用于肿瘤边界区分和手术导航的可行性。在荷LNcaP肿瘤小鼠中的微型PET/CT成像显示,[镓]Ga-NYM036在非靶器官(肾脏除外)中的蓄积相当低,而在肿瘤中的摄取较高。用10倍质量剂量的NYM036进行阻断后,肿瘤中的放射性摄取显著降低(%ID/g平均值,从20.91±3.

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