Suppr超能文献

CMKLR1 靶向肽示踪剂用于乳腺癌的 PET/MR 成像。

CMKLR1-targeting peptide tracers for PET/MR imaging of breast cancer.

机构信息

Department of Hepatology and Gastroenterology, Campus Virchow-Klinikum, Charité - Universitätsmedizin Berlin, Berlin, Germany.

Department of Nuclear Medicine, Campus Virchow-Klinikum, Charité - Universitätsmedizin Berlin, Berlin, Germany.

出版信息

Theranostics. 2019 Sep 19;9(22):6719-6733. doi: 10.7150/thno.34857. eCollection 2019.

Abstract

Molecular targeting remains to be a promising approach in oncology. Overexpression of G protein-coupled receptors (GPCRs) in human cancer is offering a powerful opportunity for tumor-selective imaging and treatment employing nuclear medicine. We utilized novel chemerin-based peptide conjugates for chemokine-like receptor 1 (CMKLR1) targeting in a breast cancer xenograft model. By conjugation with the chelator 1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetic acid (DOTA), we obtained a family of five highly specific, high-affinity tracers for hybrid positron emission tomography/magnetic resonance (PET/MR) imaging. A xenograft model with target-positive DU4475 and negative A549 tumors in immunodeficient nude mice enabled CMKLR1-specific imaging . We acquired small animal PET/MR images, assessed biodistribution by measurements and investigated the tracer specificity by blocking experiments. Five CMKLR1-targeting peptide tracers demonstrated high biological activity and affinity with EC and IC values below 2 nM. Our target-positive (DU4475) and target-negative (A549) xenograft model could be validated by analysis of CMKLR1 expression and binding. After preliminary PET imaging, the three most promising tracers [Ga]Ga-DOTA-AHX-CG34, [Ga]Ga-DOTA-KCap-CG34 and [Ga]Ga-DOTA-ADX-CG34 with best tumor uptake were further analyzed. Hybrid PET/MR imaging along with concomitant biodistribution studies revealed distinct CMKLR1-specific uptake (5.1% IA/g, 3.3% IA/g and 6.2% IA/g 1 h post-injection) of our targeted tracers in DU4475 tumor tissue. In addition, tumor uptake was blocked by excess of unlabeled peptide (6.4-fold, 5.5-fold and 3.4-fold 1 h post-injection), further confirming CMKLR1 specificity. Out of five tracers, we identified these three tracers with moderate, balanced hydrophilicity to be the most potent in receptor-mediated tumor targeting. We demonstrated the applicability of Ga-labeled peptide tracers by visualizing CMKLR1-positive breast cancer xenografts in PET/MR imaging, paving the way for developing them into theranostics for tumor treatment.

摘要

分子靶向仍然是肿瘤学中一种很有前途的方法。在人类癌症中,G 蛋白偶联受体(GPCRs)的过表达为核医学提供了一种强大的肿瘤选择性成像和治疗机会。我们利用新型趋化因子样受体 1(CMKLR1)靶向的 chemerin 基肽缀合物在乳腺癌异种移植模型中进行研究。通过与螯合剂 1,4,7,10-四氮杂环十二烷-1,4,7,10-四乙酸(DOTA)缀合,我们获得了一组五种用于杂交正电子发射断层扫描/磁共振(PET/MR)成像的高度特异性、高亲和力示踪剂。在免疫缺陷裸鼠中,我们建立了一个带有靶阳性 DU4475 和靶阴性 A549 肿瘤的异种移植模型,使 CMKLR1 特异性成像成为可能。我们获得了小动物 PET/MR 图像,通过测量评估了生物分布,并通过阻断实验研究了示踪剂的特异性。五种 CMKLR1 靶向肽示踪剂表现出高生物活性和亲和力,EC 和 IC 值低于 2 nM。我们的靶阳性(DU4475)和靶阴性(A549)异种移植模型可以通过 CMKLR1 表达和结合分析进行验证。初步 PET 成像后,进一步分析了三种最有前途的示踪剂 [Ga]Ga-DOTA-AHX-CG34、[Ga]Ga-DOTA-KCap-CG34 和 [Ga]Ga-DOTA-ADX-CG34,它们具有最佳的肿瘤摄取率。PET/MR 融合成像以及伴随的生物分布研究表明,我们的靶向示踪剂在 DU4475 肿瘤组织中有明显的 CMKLR1 特异性摄取(注射后 1 小时分别为 5.1%IA/g、3.3%IA/g 和 6.2%IA/g)。此外,肿瘤摄取被过量未标记的肽阻断(1 小时后分别为 6.4 倍、5.5 倍和 3.4 倍),进一步证实了 CMKLR1 的特异性。在这五种示踪剂中,我们确定了这三种具有中等、平衡亲水性的示踪剂在受体介导的肿瘤靶向中最有效。我们通过在 PET/MR 成像中可视化 CMKLR1 阳性乳腺癌异种移植,证明了 Ga 标记肽示踪剂的适用性,为开发用于肿瘤治疗的治疗药物奠定了基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/32b9/6771245/7cd1b14a3351/thnov09p6719g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验