Human cholangiocarcinomas express somatostatin receptors and respond to somatostatin with growth inhibition

Kiat Tan Chee Kiat Tan, Prasad V. Podila, John E. Taylor, David M. Nagorney, Gregory A. Wiseman, Gregory J. Gores, Nicholas F. Larusso

Research output: Contribution to journalArticle

46 Scopus citations

Abstract

Background/Aims: Cholangiocarcinoma, a malignancy of biliary epithelia, is usually fatal because of absence of tests for early detection and lack of effective therapy. Somatostatin (SS) receptors are expressed in several malignancies and in rodent biliary epithelia. We tested the hypothesis that SS receptors are present in cholangiocarcinomas. Methods: We examined tissue from seven surgically resected human cholangiocarcinomas and a human bile duct cancer cell line for the messenger RNA for one subtype of SS receptors (SSTR2) and studied binding and growth-active properties of SS and its analogues. Results: SSTR2 messenger RNA was expressed in all seven human cholangiocarcinoma specimens. Experiments with the human cholangiocarcinoma cell line showed specific, saturable binding of an SS analogue (MK-678) with high affinity for SSTR2 on cholangiocarcinoma membranes; inhibition in vitro of tumor cell proliferation by SS-14 and its analogue, octreotide; and inhibition in vivo of tumor growth in athymic mice implanted with human cholangiocarcinoma cells and treated with lanreotide, another SS analogue. Experiments to elucidate a possible mechanism of growth inhibition by SS showed it was not through changes in cellular cyclic adenosine monophosphate or calcium levels. Using gamma camera imaging with an 111In-SS analogue, we localized a histologically proven cholangiocarcinoma in a patient. Conclusions: These results suggest that SS analogues may be useful for diagnostic localization and treatment of biliary tract malignancies.

Original languageEnglish (US)
Pages (from-to)1908-1916
Number of pages9
JournalGastroenterology
Volume108
Issue number6
DOIs
StatePublished - Jun 1995

    Fingerprint

ASJC Scopus subject areas

  • Hepatology
  • Gastroenterology

Cite this