Rapid detection of hypoxia-inducible factor-1-active tumours: pretargeted imaging with a protein degrading in a mechanism similar to hypoxia-inducible factor-1α

Purpose Hypoxia-inducible factor-1 (HIF-1) plays an important role in malignant tumour progression. For the imaging of HIF-1-active tumours, we previously developed a protein, POS, which is effectively delivered to and selectively stabilized in HIF-1-active cells, and a radioiodinated biotin derivative, (3- 123 I-iodobenzoyl)norbiotinamide ( 123 I-IBB), which can bind to the streptavidin moiety of POS. In this study, we aimed to investigate the feasibility of the pretargeting method using POS and 123 I-IBB for rapid imaging of HIF-1-active tumours. Methods Tumour-implanted mice were pretargeted with POS. After 24 h, 125 I-IBB was administered and subsequently, the biodistribution of radioactivity was investigated at several time points. In vivo planar imaging, comparison between 125 I-IBB accumulation and HIF-1 transcriptional activity, and autoradiography were performed at 6 h after the administration of 125 I-IBB. The same sections that were used in autoradiographic analysis were subjected to HIF-1α immunohistochemistry. Results 125 I-IBB accumulation was observed in tumours of mice pretargeted with POS (1.6%ID/g at 6 h). This result is comparable to the data derived from 125 I-IBB-conjugated POS-treated mice (1.4%ID/g at 24 h). In vivo planar imaging provided clear tumour images. The tumoral accumulation of 125 I-IBB significantly correlated with HIF-1-dependent luciferase bioluminescence ( R =0.84, p