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Published on: September 16, 2019
Development of Netrin-1-targeted peptide probes derived from the Netrin-1/DCC complex for noninvasive imaging of
Shu Li1, Shuang Wang1, Xue Zhu1
1National Health Commission Key Laboratory of Nuclear Medicine, Jiangsu Key Laboratory of Molecular Nuclear Medicine, Jiangsu Institute of Nuclear Medicine, Wuxi, Jiangsu 214063, China; Department of Radiopharmaceuticals, School of Pharmacy, Nanjing Medical University, Nanjing 211166, China.
Abstract:
Netrin-1 is a secreted glycoprotein that is overexpressed in non-small cell lung cancer (NSCLC) and breast cancer, making it an emerging biomarker for tumor diagnosis and targeted therapy. However, noninvasive imaging tools for quantitative assessment of Netrin-1 expression remain limited. In this study, leveraging the crystal structure of the Netrin-1/DCC complex, we rationally designed two Netrin-1-targeted peptides YP8 and LE7, through systematic in silico molecular docking, alanine scanning, and virtual amino acid mutation. Their corresponding 68Ga-labeled PET tracers [68Ga]Ga-NOTA-YP8 and [68Ga]Ga-NOTA-LE7, were subsequently developed. Comparative evaluation revealed that [68Ga]Ga-NOTA-LE7 exhibited superior Netrin-1 binding affinity, enhanced in vivo stability, and significantly improved tumor-to-background ratio. PET imaging demonstrated specific and robust uptake of [68Ga]Ga-NOTA-LE7 in Netrin-1-positive A549 and 4T1 tumors, with minimal accumulation in Netrin-1-low MDA-MB-231 tumors. The NIRF probe ICG-LE7 further confirmed specific tumor targeting and enabled fluorescence-guided surgical resection. Collectively, these findings establish [68Ga]Ga-NOTA-LE7 and ICG-LE7 as promising noninvasive diagnostic tools for Netrin-1 expression imaging.
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