Therapeutic effect of the gastrin receptor antagonist, cr2093 on gastrointestinal tumour cell growth

Abstract

The gastrin receptor antagonist, CR2093, competed with125I-gastrin-17 (5 x 1010m) for binding to gastrin receptors on the rat pancreatic adenocarcinoma, AR42J (CR2093 concentration inducing 50% ofI25I-gastrin-17 binding (IC50) was 8 x 10-5m), on the human gastric adenocarcinoma, MKN45 (IC50 5. 5 x 10-5m) and the human colo-rectal adenocarcinoma C523 (IC50 >10-4m). Intravenous administration of CR2093 (40 mg kg-1 day-1) reduced the gastrin-17 stimulated growth of AR42J xenografts in nude mice to below that of the original basal growth (P = 0. 0166 from basal and P = 0. 0109 from gastrin stimulated growth). CR2093 administration also reduced the gastrin-stimulated growth of MKN45 xenografts (P = 0. 045) but failed to inhibit the gastrin enhanced proliferation of C523 xenografts. This may be related to the affinity (Kd) of the gastrin receptors present on the xenograft lines as the Kds of the two xenografts inhibited by CR2093 were 4. 6 x 10-10 M (AR42J) and 1. 2 x 10-9 M (MKN45) respectively whereas the Kd of C523 was of higher affinity (2. 2 x 10-° m). GR antagonists may be a viable therapeutic option for gastrin receptor positive, gastro-intestinal tumours. © 1992 Macmillan Press Ltd.