Rizzo Rebecca, Capozza Martina, Conti Laura, Avalle Lidia, Poli Valeria, Terreno Enzo
Department of Molecular Biotechnology and Health Sciences, University of Turin, Piazza Nizza 44/bis, Turin 10126, Italy.
DISIT, University of Eastern Piedmont, Viale Teresa Michel 11, Alessandria 15121, Italy.
Mol Pharm. 2025 Mar 3;22(3):1518-1528. doi: 10.1021/acs.molpharmaceut.4c01232. Epub 2025 Feb 15.
Fibroblast activation protein (FAP) is a pan-cancer target that is useful for imaging, ideally all epithelial cancers. This work aimed to develop, characterize, and validate two novel FAP-targeted probes for optical imaging, both in and . IRDye800CW and FNIRTag heptamethine cyanines were conjugated to the NH precursor of the well-known FAP inhibitor FAPI-46, which is widely employed in nuclear medicine. In addition to synthesis, the dyes were characterized in terms of physicochemical properties, biodistribution, and imaging performances in a breast cancer tumor model. FAPI-FNIRTag showed a stronger fluorescence and higher photostability compared to FAPI-IRDye800CW. Notably, both compounds exhibited strong tumor accumulation in TUBO breast cancer-bearing mice 24 h postadministration, suggesting potential for further investigation as fluorescence-guided surgery (FGS) agents.
成纤维细胞活化蛋白(FAP)是一种泛癌靶点,对成像很有用,理想情况下适用于所有上皮癌。这项工作旨在开发、表征和验证两种用于光学成像的新型FAP靶向探针,包括体内和体外研究。IRDye800CW和FNIRTag七甲川花菁与核医学中广泛使用的著名FAP抑制剂FAPI-46的NH前体偶联。除了合成外,还对染料的物理化学性质、生物分布和在乳腺癌肿瘤模型中的成像性能进行了表征。与FAPI-IRDye800CW相比,FAPI-FNIRTag显示出更强的荧光和更高的光稳定性。值得注意的是,两种化合物在给药后24小时在荷TUBO乳腺癌小鼠中均表现出强烈的肿瘤蓄积,表明它们作为荧光引导手术(FGS)试剂具有进一步研究的潜力。