Huang Wenpeng, Li Liming, Liang Yutong, Yang Qi, Mixdorf Jason C, Engle Jonathan W, Fan Yu, Kang Lei, Cai Weibo
Department of Nuclear Medicine, Peking University First Hospital, Beijing 100034, China.
Departments of Radiology and Medical Physics, University of Wisconsin─Madison, Madison, Wisconsin 53705, United States.
Mol Pharm. 2025 Jun 2;22(6):3468-3478. doi: 10.1021/acs.molpharmaceut.5c00469. Epub 2025 May 8.
Nectin4 is a tumor-associated antigen that is highly expressed in various solid tumors and is associated with tumor progression and poor prognosis. We performed an ImmunoPET imaging study to assess Nectin4 expression in gastric and bladder cancer models utilizing [Cu]Cu-NOTA-Padcev. ImmunoPET imaging confirmed significant tumor uptake at 48 h in NCI-N87 (13.83 ± 1.80% ID/g) and HT-1376 (22.97 ± 2.67% ID/g) models, which was significantly higher than in HGC-27 (5.93 ± 0.15% ID/g, = 0.0163) and UM-UC-3 (5.40 ± 0.69% ID/g, = 0.0051) models. Co-injection of [Cu]Cu-NOTA-Padcev with 2 mg of unlabeled Padcev significantly decreased tumor uptake in NCI-N87 (5.53 ± 0.59% ID/g, = 0.0097) and HT-1376 (4.97 ± 0.68% ID/g, = 0.0049), indicating receptor-specific binding. Fluorescence imaging consistently showed significantly greater tumor accumulation in the IRDye 800CW-Padcev group than in the blocking group for both the NCI-N87 model (64.05 ± 8.97 × 10 vs 10.12 ± 1.83 × 10 at 168 h for the NCI-N87 model, = 0.0072) and the HT-1376 model (99.48 ± 13.61 × 10 vs 10.12 ± 1.83 × 10 at 168 h for the HT-1376 model, = 0.0068). [Cu]Cu-NOTA-Padcev ImmunoPET imaging demonstrated specific, rapid, and prolonged accumulation in Nectin4-high tumors in both gastric and bladder cancer models.
Nectin4是一种肿瘤相关抗原,在多种实体瘤中高表达,与肿瘤进展和不良预后相关。我们进行了一项免疫正电子发射断层显像(ImmunoPET)研究,以利用[铜]Cu-NOTA-Padcev评估胃癌和膀胱癌模型中Nectin4的表达。免疫正电子发射断层显像证实,在NCI-N87(13.83±1.80%ID/g)和HT-1376(22.97±2.67%ID/g)模型中,48小时时肿瘤有显著摄取,这显著高于HGC-27(5.93±0.15%ID/g,P=0.0163)和UM-UC-3(5.40±0.69%ID/g,P=0.0051)模型。将[铜]Cu-NOTA-Padcev与2毫克未标记的Padcev共同注射,显著降低了NCI-N87(5.53±0.59%ID/g,P=0.0097)和HT-1376(4.97±0.68%ID/g,P=0.0049)的肿瘤摄取,表明存在受体特异性结合。荧光成像一致显示,对于NCI-N87模型(168小时时为64.05±8.97×10对10.12±1.83×10,P=0.0072)和HT-1376模型(168小时时为99.48±13.61×10对10.12±1.83×10,P=0.0068),IRDye 800CW-Padcev组的肿瘤蓄积明显高于阻断组。[铜]Cu-NOTA-Padcev免疫正电子发射断层显像显示,在胃癌和膀胱癌模型中,Nectin4高表达的肿瘤中均有特异性、快速和持续的蓄积。