Abstract
Fluorescence molecular imaging plays a vital role in image-guided surgery. In this context, the urokinase plasminogen activator receptor (uPAR) is an interesting biomarker enabling the detection and delineation of various tumor types due to its elevated expression on both tumor cells and the tumor microenvironment. In this study, anti-uPAR Nanobodies (Nbs) are generated through llama immunization with human and murine uPAR protein. Extensive in vitro characterization and in vivo testing with radiolabeled variants are conducted to assess their pharmacokinetics and select lead compounds. Subsequently, the selected Nbs are converted into fluorescent agents, and their application for fluorescence-guided surgery is evaluated in various subcutaneous and orthotopic tumor models. The study yields a panel of high-affinity anti-uPAR Nbs, showing specific binding across multiple types of cancer cells in vitro and in vivo. Lead fluorescently-labeled compounds exhibit high tumor uptake with high contrast at 1 h after intravenous injection across all assessed uPAR-expressing tumor models, outperforming a non-targeting control Nb. Additionally, rapid and accurate tumor localization and demarcation are demonstrated in an orthotopic human glioma model. Utilizing these Nbs can potentially enhance the precision of surgical tumor resection and, consequently, improve survival rates in the clinic.
Original language | English |
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Article number | e2400700 |
Number of pages | 11 |
Journal | Advanced Science |
Volume | 11 |
Issue number | 30 |
Early online date | 6 Jun 2024 |
DOIs | |
Publication status | Published - Aug 2024 |
Bibliographical note
Funding Information:The authors thank Jan de Jonge, Kevin De Jonghe, and Sofie Pollenus for their technical assistance during the experiments. This work was supported by Stichting Tegen Kanker (grant number ANI183), Research Foundation \u2013 Flanders: Research Infrastructure program Hercules and Strategic Basic Research program (grant number FWOSBO42), Strategic Research Program (grant number SRP50), Innovation Research Fund (grant number IOF3005).
Publisher Copyright:
© 2024 The Authors. Advanced Science published by Wiley-VCH GmbH.