Department of Obstetrics and Gynecology, National Clinical Research Center for Obstetrics and Gynecology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China; Key Laboratory of Cancer Invasion and Metastasis (Ministry of Education), Hubei Key Laboratory of Tumor Invasion and Metastasis, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China; Cancer Center, Renmin Hospital of Wuhan University, Wuhan 430060, China.
Department of Obstetrics and Gynecology, National Clinical Research Center for Obstetrics and Gynecology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China; Key Laboratory of Cancer Invasion and Metastasis (Ministry of Education), Hubei Key Laboratory of Tumor Invasion and Metastasis, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Biomed Pharmacother. 2024 Aug;177:116980. doi: 10.1016/j.biopha.2024.116980. Epub 2024 Jun 21.
Lymphangiogenesis at primary tumor and draining lymph nodes plays a pivotal role in tumor metastasis, which has been demonstrated to be regulated by the vascular endothelial growth factor receptor 3 (VEGFR-3) pathway. However, the effect of molecular imaging peptides, which specifically bind VEGFR-3, in tracing tumors remains unclear. We prepared a novel peptide, TMVP1448, with high-affinity to VEGFR-3. The dissociation constant (KD) of TMVP1448 with VEGFR-3 was 7.07 ×10-7 M. In vitro cellular assay showed that TMVP1448 could bind specifically with VEGFR-3. Near infrared imaging results showed that Cy7-TMVP1448 was able to accurately trace primary and metastatic cancers, and PET/CT results showed that [Ga]Ga-DOTA-TMVP1448 was superior to commonly used radiotracers F-FDG. Additionally, no significant negative effect of TMVP1448 was found in mice. Our results suggested that TMVP1448 had great potential for future clinical applications in fluorescence imaging and nuclear imaging of tumors.
淋巴管生成在原发性肿瘤和引流淋巴结中起着关键作用,促进肿瘤转移,这已被证明受血管内皮生长因子受体 3(VEGFR-3)途径调控。然而,特异性结合 VEGFR-3 的分子成像肽在追踪肿瘤方面的效果尚不清楚。我们制备了一种新型肽 TMVP1448,它对 VEGFR-3 具有高亲和力。TMVP1448 与 VEGFR-3 的解离常数(KD)为 7.07×10-7 M。体外细胞试验表明,TMVP1448 可以特异性结合 VEGFR-3。近红外成像结果表明,Cy7-TMVP1448 能够准确追踪原发性和转移性癌症,而 PET/CT 结果表明,[Ga]Ga-DOTA-TMVP1448 优于常用的放射性示踪剂 F-FDG。此外,TMVP1448 在小鼠中没有发现明显的负面作用。我们的研究结果表明,TMVP1448 在肿瘤的荧光成像和核医学成像的未来临床应用中具有巨大的潜力。