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Enzyme‐activatable dual‐locked fluorescent probe for precision imaging of cutaneous squamous cell carcinoma

2025/09/01 by Yanhua Li, Shan Zuo, Yushi Chen +3 · 1 voice
Biochemistry, Genetics and Molecular Biology · Engineering · Medicine · #Nanoplatforms for cancer theranostics #Peptidase Inhibition and Analysis #Protease and Inhibitor Mechanisms

paper · pdf · doi:10.1002/smo2.70018

openalex publication_date 2025/09/01 · openalex created_date 2025/10/10 · openalex updated_date 2026/07/17

Abstract

Abstract Cutaneous squamous cell carcinoma (cSCC), the second most common skin cancer, requires early and accurate detection to optimize clinical management. Fluorescence imaging has emerged as a non‐invasive and cost‐effective tool with high sensitivity for tumor diagnosis; however, existing probes for cSCC are limited in achieving rapid and specific imaging. In this study, we introduce FC‐1 , a dual‐tandem activatable fluorescent probe designed for precise cSCC diagnosis by simultaneously targeting fibroblast activation protein α and cathepsin C (CTSC). This dual‐locked activation strategy effectively reduces nonspecific signals in normal tissues while enhancing diagnostic specificity. In vivo studies in SCC‐7 xenografted mice demonstrated FC‐1 's ability to visualize subcutaneous tumors with high sensitivity and specificity. Moreover, FC‐1 enabled clear differentiation between cSCC and keloids. The probe's dual‐activation mechanism and robust performance underscore its potential as a clinically translatable tool for early cSCC detection and differential diagnosis.

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