Expression and ligand binding of bombesin receptors in pulmonary and intestinal carcinoids

Introduction: Carcinoids are mainly found in the gastrointestinal (65%) and bronchopulmonary tract (25%). These neuroendocrine tumors secrete a wide range of bioactive peptides, including gastrin releasing peptide and neuromedin B, the mammalian analogs of bombesin. The purpose of this study was to...

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Veröffentlicht in:Journal of endocrinological investigation 2011-10, Vol.34 (9), p.665-670
Hauptverfasser: Kuiper, P., Verspaget, H. W., Biemond, I., de Jonge-Muller, E. S., van Eeden, S., van Velthuysen, M.-L. F., Taal, B. G., Lamers, C. B.
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container_end_page 670
container_issue 9
container_start_page 665
container_title Journal of endocrinological investigation
container_volume 34
creator Kuiper, P.
Verspaget, H. W.
Biemond, I.
de Jonge-Muller, E. S.
van Eeden, S.
van Velthuysen, M.-L. F.
Taal, B. G.
Lamers, C. B.
description Introduction: Carcinoids are mainly found in the gastrointestinal (65%) and bronchopulmonary tract (25%). These neuroendocrine tumors secrete a wide range of bioactive peptides, including gastrin releasing peptide and neuromedin B, the mammalian analogs of bombesin. The purpose of this study was to investigate the quantity and localization of bombesin receptors in gastrointestinal and pulmonary carcinoids, and to reveal whether bombesin-like peptides (BLP) and their receptors are of any value in distinguishing pulmonary carcinoids from carcinoids of intestinal origin. Methods: Carcinoid tumors with pulmonary (no.=9) or intestinal (no.=15) localizations were analyzed by immunohistochemistry, autoradiography, and radioimmunoassay, to examine the presence of bombesin receptor subtypes and determine BLP levels in these tumors. Results: All 3 bombesin receptor subtypes (GRPR, NM-BR, and BRS-3) were present on pulmonary and intestinal carcinoids by immunohistochemistry. In pulmonary carcinoids, low receptor ligand binding densities together with high and low BLP levels were found. Intestinal carcinoids showed predominantly high receptor ligand binding densities in combination with low BLP levels. Conclusions: The expression of bombesin receptor subtypes is independent from the carcinoid tumor origin, and is therefore not recommended as a distinction marker, although carcinoids of pulmonary and intestinal origin possess different receptor binding affinities for bombesin and dissimilar BLP levels. The combined presence of bombesin and its receptors might suggest the presence of a paracrine or autocrine growth loop in carcinoids.
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W. ; Biemond, I. ; de Jonge-Muller, E. S. ; van Eeden, S. ; van Velthuysen, M.-L. F. ; Taal, B. G. ; Lamers, C. B.</creator><creatorcontrib>Kuiper, P. ; Verspaget, H. W. ; Biemond, I. ; de Jonge-Muller, E. S. ; van Eeden, S. ; van Velthuysen, M.-L. F. ; Taal, B. G. ; Lamers, C. B.</creatorcontrib><description>Introduction: Carcinoids are mainly found in the gastrointestinal (65%) and bronchopulmonary tract (25%). These neuroendocrine tumors secrete a wide range of bioactive peptides, including gastrin releasing peptide and neuromedin B, the mammalian analogs of bombesin. The purpose of this study was to investigate the quantity and localization of bombesin receptors in gastrointestinal and pulmonary carcinoids, and to reveal whether bombesin-like peptides (BLP) and their receptors are of any value in distinguishing pulmonary carcinoids from carcinoids of intestinal origin. Methods: Carcinoid tumors with pulmonary (no.=9) or intestinal (no.=15) localizations were analyzed by immunohistochemistry, autoradiography, and radioimmunoassay, to examine the presence of bombesin receptor subtypes and determine BLP levels in these tumors. Results: All 3 bombesin receptor subtypes (GRPR, NM-BR, and BRS-3) were present on pulmonary and intestinal carcinoids by immunohistochemistry. In pulmonary carcinoids, low receptor ligand binding densities together with high and low BLP levels were found. Intestinal carcinoids showed predominantly high receptor ligand binding densities in combination with low BLP levels. Conclusions: The expression of bombesin receptor subtypes is independent from the carcinoid tumor origin, and is therefore not recommended as a distinction marker, although carcinoids of pulmonary and intestinal origin possess different receptor binding affinities for bombesin and dissimilar BLP levels. The combined presence of bombesin and its receptors might suggest the presence of a paracrine or autocrine growth loop in carcinoids.</description><identifier>ISSN: 0391-4097</identifier><identifier>EISSN: 1720-8386</identifier><identifier>DOI: 10.3275/7332</identifier><identifier>PMID: 21060250</identifier><language>eng</language><publisher>Cham: Springer International Publishing</publisher><subject>Bombesin - analogs &amp; derivatives ; Bombesin - metabolism ; Carcinoid Tumor - metabolism ; Carcinoid Tumor - pathology ; Endocrinology ; Humans ; Intestinal Neoplasms - metabolism ; Intestinal Neoplasms - pathology ; Ligands ; Lung Neoplasms - metabolism ; Lung Neoplasms - pathology ; Medicine ; Medicine &amp; Public Health ; Metabolic Diseases ; Original Articles ; Protein Isoforms - metabolism ; Receptors, Bombesin - metabolism</subject><ispartof>Journal of endocrinological investigation, 2011-10, Vol.34 (9), p.665-670</ispartof><rights>Italian Society of Endocrinology (SIE) 2011</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-p240t-8c94b9d06b53cf0985d67131221cdfb5fdb51b0b135f65efc6d948a476226d203</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.3275/7332$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.3275/7332$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,41488,42557,51319</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21060250$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kuiper, P.</creatorcontrib><creatorcontrib>Verspaget, H. W.</creatorcontrib><creatorcontrib>Biemond, I.</creatorcontrib><creatorcontrib>de Jonge-Muller, E. S.</creatorcontrib><creatorcontrib>van Eeden, S.</creatorcontrib><creatorcontrib>van Velthuysen, M.-L. F.</creatorcontrib><creatorcontrib>Taal, B. G.</creatorcontrib><creatorcontrib>Lamers, C. B.</creatorcontrib><title>Expression and ligand binding of bombesin receptors in pulmonary and intestinal carcinoids</title><title>Journal of endocrinological investigation</title><addtitle>J Endocrinol Invest</addtitle><addtitle>J Endocrinol Invest</addtitle><description>Introduction: Carcinoids are mainly found in the gastrointestinal (65%) and bronchopulmonary tract (25%). These neuroendocrine tumors secrete a wide range of bioactive peptides, including gastrin releasing peptide and neuromedin B, the mammalian analogs of bombesin. The purpose of this study was to investigate the quantity and localization of bombesin receptors in gastrointestinal and pulmonary carcinoids, and to reveal whether bombesin-like peptides (BLP) and their receptors are of any value in distinguishing pulmonary carcinoids from carcinoids of intestinal origin. Methods: Carcinoid tumors with pulmonary (no.=9) or intestinal (no.=15) localizations were analyzed by immunohistochemistry, autoradiography, and radioimmunoassay, to examine the presence of bombesin receptor subtypes and determine BLP levels in these tumors. Results: All 3 bombesin receptor subtypes (GRPR, NM-BR, and BRS-3) were present on pulmonary and intestinal carcinoids by immunohistochemistry. In pulmonary carcinoids, low receptor ligand binding densities together with high and low BLP levels were found. Intestinal carcinoids showed predominantly high receptor ligand binding densities in combination with low BLP levels. Conclusions: The expression of bombesin receptor subtypes is independent from the carcinoid tumor origin, and is therefore not recommended as a distinction marker, although carcinoids of pulmonary and intestinal origin possess different receptor binding affinities for bombesin and dissimilar BLP levels. 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subjects Bombesin - analogs & derivatives
Bombesin - metabolism
Carcinoid Tumor - metabolism
Carcinoid Tumor - pathology
Endocrinology
Humans
Intestinal Neoplasms - metabolism
Intestinal Neoplasms - pathology
Ligands
Lung Neoplasms - metabolism
Lung Neoplasms - pathology
Medicine
Medicine & Public Health
Metabolic Diseases
Original Articles
Protein Isoforms - metabolism
Receptors, Bombesin - metabolism
title Expression and ligand binding of bombesin receptors in pulmonary and intestinal carcinoids
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