期刊
CLINICAL CANCER RESEARCH
卷 15, 期 16, 页码 5240-5249出版社
AMER ASSOC CANCER RESEARCH
DOI: 10.1158/1078-0432.CCR-08-3145
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资金
- Swiss Cancer League [OCS-01778-08-2005]
- Swiss National Science Foundation [320000-118333]
Purpose: G protein-coupled receptor agonists are being used as radiolabeled vectors for in vivo localization and therapy of tumors. Recently, somatostatin-based antagonists were shown to be superior to agonists. Here, we compare the new [In-111/Ga-68]-labeled bombesin-based antagonist RM1 with the agonist [In-111]-AMBA for targeting the gastrin-releasing peptide receptor (GRPR). Experimental Design: IC50, K-d values, and antagonist potency were determined using PC-3 and HEK-GRPR cells. Biodistribution and imaging studies were done in nude mice transplanted with the PC-3 tumor. The antagonist potency was assessed by evaluating the effects on calcium release and on receptor internalization monitored by immunofluorescence microscopy. Results: The IC50 value of [In-nat]-RM1 was 14 +/- 3.4 nmol/L. [In-nat/111]-RM1 was found to bind to the GRPR with a K-d of 8.5 +/- 2.7 nmol/L compared with a K-d of 0.6 +/- 0.3 nmol/L of [In-111]-AMBA. A higher maximum number of binding site value was observed for [In-111]-RM1 (2.4 +/- 0.2 nmol/L) compared with [In-111]-AMBA(0.7 +/- 0.1 nmol/L). [Lu-nat]-AMBA is a potent agonist in the immunofluorescence-based internalization assay, whereas [In-nat]-RM1 is inactive alone but efficiently antagonizes the bombesin effect. These data are confirmed by the calcium release assay. The pharmacokinetics showed a superiority of the radioantagonist with regard to the high tumor uptake (13.4 +/- 0.8% IA/g versus 3.69 +/- 0.75% IA/g at 4 hours after injection. as well as to all tumor-to-normal tissue ratios. Conclusion: Despite their relatively low GRPR affinity, the antagonists [In-111/68 Ga]-RM1 showed superior targeting properties compared with [In-111]-AMBA. As found for somatostatin receptor-targeting radiopeptides, GRP-based radioantagonists seem to be superior to radioagonists for in vivo imaging and potentially also for targeted radiotherapy of GRPR-positive tumors. (Clin Cancer Res 2009;15(16):5240-9)
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