Q1 · MEDICINE
Article
Author: Resnati, Massimo ; Pelger, Rob C M ; Kuppen, Peter J K ; Baart, Victor M ; Sier, Cornelis F M ; Mazar, Andrew P ; de Jonge, Hugo ; Iamele, Luisa ; van der Horst, Geertje ; van der Pluijm, Gabriel ; van der Mark, Maaike H ; Bhairosingh, Shadhvi S ; Schomann, Timo ; Vahrmeijer, Alexander L ; Deken, Marion M ; Sier, Vincent Q
METHODS:Expression of urokinase plasminogen activator receptor (uPAR) and epithelial cell adhesion molecule (EpCAM) are determined on paraffin-embedded human UCC using immunohistochemistry and on UCC cell lines by flow cytometry. MNPR-101, a humanised monoclonal antibody targeting uPAR is conjugated to IRDye800CW and binding is validated in vitro using surface plasmon resonance and cell-based binding assays. In vivo NIR fluorescence and photoacoustic three-dimensional (3D) imaging are performed with subcutaneously growing human UM-UC-3luc2 cells in BALB/c-nude mice. The translational potential is confirmed in a metastasising UM-UC-3luc2 orthotopic mouse model. Infliximab-IRDye800CW and rituximab-IRDye800CW are used as controls.
RESULTS:UCCs show prominent uPAR expression at the tumour-stroma interface and EpCAM on epithelial cells. uPAR and EpCAM are expressed by 6/7 and 4/7 UCC cell lines, respectively. In vitro, MNPR-101-IRDye800CW has a picomolar affinity for domain 2-3 of uPAR. In vivo fluorescence imaging with MNPR-101-IRDye800CW, specifically delineates both subcutaneous and orthotopic tumours with tumour-to-background ratios reaching as high as 6.8, differing significantly from controls (p < 0.0001). Photoacoustic 3D in depth imaging confirms the homogenous distribution of MNPR-101-IRDye800CW through the tumour.
CONCLUSIONS:MNPR-101-IRDye800CW is suitable for multimodal imaging of UCC, awaiting clinical translation.