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内容記述 |
Galectin-3 is associated with aggression, proliferation, and metastasis in various refractory cancers. Although galectin-3 targeted positron emission tomography (PET) tracers have shown considerable promise for cancer diagnosis, the therapeutic potential of galectin-3-directed radiopharmaceutical therapy for refractory or untreatable malignancies remains largely unexplored. This study aimed to develop novel galectin-3-targeted radioimmunoligands and verify their radiotheranostic potential in multiple tumor models. Two novel galectin-3 targeted monoclonal antibodies (QMAb-1 and QMAb-2) were labeled with both 89Zr and 177Lu. PET/CT imaging of [89Zr]Zr-DFO-QMAb-1 and [89Zr]Zr-DFO-QMAb2 were evaluated in mouse tumor models with varying galectin-3 expression levels. Besides, the therapeutic efficacy of [177Lu]Lu-DTPA-QMAb-1 and [177Lu]Lu-DTPA-QMAb-2 was also investigated.The superior tumor uptake and retention time of [89Zr]Zr-DFO-QMAb-1 was observed. Notably, [89Zr]Zr-DFO-QMAb-1 demonstrated minimal off-target accumulation and rapid clearance from the bloodstream and major organs. Furthermore, [177Lu]Lu-DTPA-QMAb-1 showed potent anti-tumor efficacy without inducing hematotoxicity and major organ damage, highlighting its therapeutic potential and safety profile. This study expands the repertoire of the galectin-3 radiopharmaceutical toolbox by harnessing high affinity mAbs as ligands, offering a new modality for the diagnosis and treatment of galectin-3-positive cancers. In addition, the favorable performance of [89Zr]Zr-DFO-QMAb-1 and [177Lu]LuDTPA-QMAb-1 theranostic pair in triple-negative breast cancer models further supports their clinical application potential across a range of refractory malignancies. |
