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A transplantable human ca… - University of Gothenburg, Sweden Till startsida
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A transplantable human carcinoid as model for somatostatin receptor-mediated and amine transporter-mediated radionuclide uptake.

Journal article
Authors Lars Kölby
Peter Bernhardt
Håkan Ahlman
Bo Wängberg
V Johanson
A Wigander
Eva Forssell-Aronsson
S Karlsson
B Ahrén
G Stenman
Ola Nilsson
Published in The American journal of pathology
Volume 158
Issue 2
Pages 745-55
ISSN 0002-9440
Publication year 2001
Published at Institute of Selected Clinical Sciences, Department of Radiation Physics
Institute of Surgical Sciences, Department of Surgery
Pages 745-55
Language en
Keywords 3-Iodobenzylguanidine, pharmacokinetics, 5-Hydroxytryptophan, secretion, Animals, Biogenic Amines, metabolism, Calcium, metabolism, Carcinoid Tumor, metabolism, pathology, Carrier Proteins, metabolism, Chromogranin A, Chromogranins, analysis, Chromosome Painting, Disease Models, Animal, Female, Gene Expression Regulation, Neoplastic, Humans, Hydroxyindoleacetic Acid, metabolism, Ileal Neoplasms, metabolism, pathology, Immunohistochemistry, Male, Membrane Glycoproteins, analysis, Membrane Transport Proteins, Mice, Mice, Nude, Middle Aged, Neuropeptides, Octreotide, pharmacokinetics, RNA, Messenger, genetics, metabolism, Radioisotopes, diagnostic use, pharmacokinetics, Receptors, Somatostatin, genetics, metabolism, Serotonin, analysis, secretion, Substance P, analysis, Transplantation, Heterologous, Tumor Cells, Cultured, metabolism, Vesicular Biogenic Amine Transport Proteins, Vesicular Monoamine Transport Proteins
Subject categories Cancer and Oncology


A human midgut carcinoid tumor was successfully transplanted into nude mice and propagated for five consecutive generations (30 months) with well-preserved phenotype. Tumor cells in nude mice expressed identical neuroendocrine markers as the original tumor, including somatostatin receptors (somatostatin receptors 1 to 5) and vesicular monoamine transporters (VMAT1 and VMAT2). Because of the expression of somatostatin receptors and VMAT1 and VMAT2 the grafted tumors could be visualized scintigraphically using the somatostatin analogue 111In-octreotide and the catecholamine analogue 123I-metaiodobenzylguanidine. The biokinetics of the somatostatin analogue 111In-octreotide in the tumors was studied and showed a high retention 7 days after administration. Cell cultures were re-established from transplanted tumors. Immunocytochemical and ultrastructural studies confirmed the neuroendocrine differentiation. The human origin of transplanted tumor cells was confirmed by cytogenetic and fluorescence it situ hybridization analyses. Spontaneous secretion of serotonin and its metabolite, 5-hydroxyindole acetic acid, from tumor cells was demonstrated. The tumor cells increased their [Ca2+]i in response to beta-adrenoceptor stimulation (isoproterenol) and K+-depolarization. All somatostatin receptor subtypes could be demonstrated in cultured cells. This human transplantable carcinoid tumor, designated GOT1, grafted to nude mice, will give unique possibilities for studies of somatostatin receptor- and VMAT-mediated radionuclide uptake as well as for studies of secretory mechanisms.

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