Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Department of Biochemistry and Molecular Biology, Peking University Cancer Hospital and Institute, Beijing 100142, China.
Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), NMPA Key Laboratory for Research and Evaluation of Radiopharmaceuticals (National Medical Products Administration), Department of Nuclear Medicine, Peking University Cancer Hospital and Institute, Beijing 100142, China.
Mol Pharm. 2022 Oct 3;19(10):3530-3541. doi: 10.1021/acs.molpharmaceut.1c00947. Epub 2022 Mar 28.
Claudin 18.2 (CLDN18.2) is a new potential target for cancer therapy, especially for advanced gastric cancer (AGC). A molecular targeting probe is of importance for patient stratification and therapeutic guidance. Here, we explored an antibody-dependent molecular imaging strategy for specific detection and surgery guidance based on a CLDN18.2-specific antibody, 5C9. Two imaging probes, I-5C9 and Cy5.5-5C9, were synthesized. The specificity to CLDN18.2 being evidenced in the cellular experiments with control, the diagnostic utility was assessed by immunopositron emission tomography (immuno-PET) and fluorescence imaging using xenograft models. A near-infrared fluorescent II imaging probe FD1080-5C9 was designed to facilitate the comprehensive surgical removal of lesions. I-5C9 immuno-PET imaging clearly delineated subcutaneous CLDN18.2-positive tumors, with a peak uptake (maximum standardized uptake value; SUVmax) of 2.25 ± 0.30, whereas the highest values for the I-IgG and blocking groups were 0.70 ± 0.13 and 0.66 ± 0.12, respectively. Cy5.5-5C9 fluorescence imaging showed similar results. As proof of the diagnosis and guided surgery (DGS) concept, I-5C9 and FD1080-5C9 were simultaneously administered in orthotopic CLDN18.2-positive tumor models, facilitating the comprehensive resection of tumor tissue. Combined, I-5C9 and FD1080-5C9 are both promising DGS tools: the former reveals CLDN18.2 in lesions as a PET probe, and the latter can guide surgery. These results provide a utility molecular imaging strategy for specific detection and surgery guidance based on a CLDN18.2-specific antibody both in AGC and other cancers.
Claudin 18.2 (CLDN18.2) 是癌症治疗的一个新的潜在靶点,特别是对于晚期胃癌 (AGC)。分子靶向探针对于患者分层和治疗指导很重要。在这里,我们探索了一种基于 CLDN18.2 特异性抗体 5C9 的抗体依赖性分子成像策略,用于特异性检测和手术指导。合成了两种成像探针,I-5C9 和 Cy5.5-5C9。在细胞实验中,用对照物证明了对 CLDN18.2 的特异性,通过免疫正电子发射断层扫描 (immuno-PET) 和荧光成像在异种移植模型中评估了诊断效用。设计了一种近红外荧光 II 成像探针 FD1080-5C9,以促进病变的全面手术切除。I-5C9 immuno-PET 成像清楚地描绘了皮下 CLDN18.2 阳性肿瘤,摄取峰值(最大标准化摄取值;SUVmax)为 2.25 ± 0.30,而 I-IgG 和阻断组的最高值分别为 0.70 ± 0.13 和 0.66 ± 0.12。Cy5.5-5C9 荧光成像也显示了类似的结果。作为诊断和引导手术 (DGS) 概念的证明,在原位 CLDN18.2 阳性肿瘤模型中同时给予 I-5C9 和 FD1080-5C9,有助于全面切除肿瘤组织。总之,I-5C9 和 FD1080-5C9 都是很有前途的 DGS 工具:前者作为 PET 探针在病变中揭示 CLDN18.2,后者可以指导手术。这些结果为基于 CLDN18.2 特异性抗体的 AGC 和其他癌症的特异性检测和手术指导提供了一种实用的分子成像策略。