Bendre Shreya, Merkens Helen, Kuo Hsiou-Ting, Ng Pauline, Wong Antonio A W L, Lau Wing Sum, Zhang Zhengxing, Kurkowska Sara, Chen Chao-Cheng, Uribe Carlos, Bénard François, Lin Kuo-Shyan
Department of Molecular Oncology, BC Cancer Research Institute, Vancouver, BC, V5Z1L3, Canada.
Department of Integrative Oncology, BC Cancer Research Institute, Vancouver, BC, V5Z1L3, Canada.
Eur J Med Chem. 2024 Mar 15;268:116238. doi: 10.1016/j.ejmech.2024.116238. Epub 2024 Feb 13.
Fibroblast activation protein-α (FAP) is a marker of cancer-associated fibroblasts (CAFs) that constitute a significant portion of most carcinomas. Since it plays a critical role in tumor growth and metastasis, its timely detection to identify tumor lesions in early developmental stages using targeted radiopharmaceuticals has gained significant impetus. In the present work, two novel FAP-targeted precursors SB03178 and SB04033 comprising of an atypical benzo[h]quinoline construct were synthesized and either chelated to diagnostic radionuclide gallium-68 or therapeutic radionuclide lutetium-177, with ≥90% radiochemical purities and 22-76% decay-corrected radiochemical yields. Ga-labeled complexes displayed dose-dependent FAP inhibition, with binding potency of Ga-SB03178 being ∼17 times higher than Ga-SB04033. To evaluate their pharmacokinetic profiles, PET imaging and ex vivo biodistribution analyses were executed in FAP-overexpressing HEK293T:hFAP tumor-bearing mice. While both tracers displayed clear tumor visualization that was primarily FAP-arbitrated, with negligible uptake in most peripheral tissues, [Ga]Ga-SB03178 demonstrated higher tumor uptake and superior tumor-to-background contrast ratios than [Ga]Ga-SB04033. Lu-labeled SB03178 was subjected to tumor retention studies, mouse dosimetry profiling and mouse-to-human dose extrapolations also using the HEK293T:hFAP tumor model. [Lu]Lu-SB03178 exhibited a combination of high and sustained tumor uptake, with excellent tumor-to-critical organ uptake ratios resulting in a high radiation absorbed dose to the tumor and a low estimated whole-body dose to humans. Our preliminary findings are considerably encouraging to support clinical development of [Ga]Ga-/[Lu]Lu-SB03178 theranostic pair for use in a vast majority of FAP-overexpressing neoplasms, particularly carcinomas.
成纤维细胞活化蛋白-α(FAP)是癌症相关成纤维细胞(CAF)的标志物,CAF在大多数癌症中占很大比例。由于其在肿瘤生长和转移中起关键作用,因此使用靶向放射性药物及时检测以在早期发育阶段识别肿瘤病变已获得显著推动。在本研究中,合成了两种新型的靶向FAP的前体SB03178和SB04033,它们由非典型苯并[h]喹啉构建体组成,并与诊断性放射性核素镓-68或治疗性放射性核素镥-177螯合,放射化学纯度≥90%,衰变校正后的放射化学产率为22-76%。镓标记的复合物表现出剂量依赖性的FAP抑制作用,Ga-SB03178的结合效力比Ga-SB04033高约17倍。为了评估它们的药代动力学特征,在过表达FAP的HEK293T:hFAP荷瘤小鼠中进行了PET成像和离体生物分布分析。虽然两种示踪剂都显示出清晰的肿瘤可视化,这主要是由FAP介导的,在大多数外周组织中的摄取可忽略不计,但[Ga]Ga-SB03178比[Ga]Ga-SB04033表现出更高的肿瘤摄取和更好的肿瘤与背景对比率。镥标记的SB03178也使用HEK293T:hFAP肿瘤模型进行了肿瘤滞留研究、小鼠剂量学分析和从小鼠到人的剂量外推。[Lu]Lu-SB03178表现出高且持续的肿瘤摄取,具有出色的肿瘤与关键器官摄取比率,导致肿瘤的辐射吸收剂量高,对人的估计全身剂量低。我们的初步研究结果相当令人鼓舞,支持[Ga]Ga-/[Lu]Lu-SB03178治疗诊断对在绝大多数过表达FAP的肿瘤,特别是癌症中的临床开发。