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Assessment shows superior imaging of HMGB1-positive tumors using [68Ga]Ga-HM, suggesting better diagnostic applications.
High mobility group box 1 (HMGB1) is highly expressed in various malignancies and has been considered as a promising molecular target for cancer diagnosis and therapy. In this study, two novel peptide-based radiotracers targeting HMGB1 were synthesized, each achieving high radiochemical purity (>95%). Of these tracers, [68Ga]Ga-HM possessed superior characteristics with a high binding affinity for the PC3 cell line (Kd = 46.11 ± 0.97 nM). Micro-PET imaging and biodistribution investigation in PC3 tumor-bearing mice revealed significant tumor uptake (SUVmax = 1.52 ± 0.10) and an excellent tumor-to-muscle ratio (6.96 ± 0.64) at 30 min post-injection. Moreover, robust imaging performance and favorable biodistribution profiles were consistently observed for [68Ga]Ga-HM across multiple distinct HMGB1-positive tumor models. These findings demonstrate that [68Ga]Ga-HM could serve as a diagnostic tracer to identify tumors with high HMGB1 expression, enabling personalized cancer treatment through the selection and monitoring of targeted therapeutic approaches.
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Wang et al. (2025) studied this question.
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