TumorDiagnostik & Therapie 2001; 22(1): 1-13
DOI: 10.1055/s-2001-12745
ÜBERSICHT/REVIEW
© Georg Thieme Verlag Stuttgart · New York

Die Bedeutung von Peptidhormonen des Magen-Darm-Trakts
für das Wachstum von humanen gastrointestinalen Tumoren[*]

The Role of Gastrointestinal Hormones for the Growth of Gastrointestinal MalignanciesCh. Lersch, J. Erdmann, V. Schusdziarra
  • II. Medizinische Klinik und Poliklinik der Technischen Universität München, Klinikum rechts der Isar
Further Information

Publication History

Publication Date:
31 December 2001 (online)

Zusammenfassung.

Rezeptoren für Peptidhormone wurden auf Tumoren und Tumorzelllinien des Gastrointestinaltrakts nachgewiesen. In der Übersicht werden Daten über Peptide, für deren Agonisten bzw. Antagonisten Wirkungen bei humanen Tumoren gezeigt wurden, zusammenfassend dargestellt. Gastrin-Antagonisten können das Wachstum von Pankreas- und Kolonkarzinomzelllinien in vitro und in Nacktmäusen hemmen, nicht dagegen bisher bei Patienten mit Pankreas- und Magenkarzinomen. Eine Rolle des Gastrins bei der Karzinogenese des Magen- und Kolonkarzinoms wird diskutiert. Weder Cholezystokinin-Antagonisten noch -agonisten konnten das Wachstum von Pankreaskarzinomen bei Patienten hemmen. Über Neurotensin-Rezeptoren kann in vitro das Wachstum von Kolon- und Pankreaszelllinien gesteigert werden. Vasoaktives Intestinales Peptid (VIP) beeinflusst das Wachstum von humanen gastrointestinalen Tumoren unterschiedlich. Das Peptid YY kann das Wachstum humaner Pankreas- und Kolonkarzinomzelllinien hemmen. Der Einsatz von Somatostatin und Analoga bei neuronendokrinen Tumoren ist etabliert. Auch bei Kolonkarzinomen und deren Vorläufern sowie beim hepatozellulären Karzinom könnten diese Substanzen wirksam sein.

The Role of Gastrointestinal Hormones for the Growth of Gastrointestinal Malignancies.

Receptors for regulatory gut/brain peptides are expressed on gastrointestinal tumors and tumor cell lines. This review summarizes data on those agonists and antagonists of peptides which effect the growth of human gastrointestinal tumors. Growth of pancreatic and colon carcinomas is retarded by gastrin and its agonists in vitro and in nude mice but not in men. A significant role of gastrin in human colorectal and stomach cancers has recently been discussed. Cholecystokinin and its agonists/antagonists did not stop the growth of pancreatic carcinomas in patients. In vitro growth of pancreatic and colon cancer cell lines could be stimulated via receptors for neurotensin. Vasoactive intestinal peptide (VIP) has ambivalent effects on the growth of gastrointestinal tumors. Peptide YY decreases the growth of human pancreatic and colon cancer cell lines. Somatostatin and its agonists are successfully used for therapy of neuroendocrine tumors. They also could be effective in therapy of colon and hepatocellular carcinomas.

1 Diese Arbeit wird von der Sander Stiftung unterstützt.

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1 Diese Arbeit wird von der Sander Stiftung unterstützt.

Christian Lersch

II. Medizinische Klinik und Poliklinik
der Technischen Universität München
Klinikum rechts der Isar

Ismaninger Straße 22

81675 München

Phone: 089-4140-2482

Fax: 089-4140-4968

Email: christian.lersch@lrz.tum.de

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