Gastrin increases its own synthesis in gastrointestinal cancer cells via the CCK2 receptor

FEBS Lett. 2010 Nov 5;584(21):4413-8. doi: 10.1016/j.febslet.2010.09.046. Epub 2010 Oct 8.

Abstract

The involvement of the gastrointestinal hormone gastrin in the development of gastrointestinal cancer is highly controversial. Here we demonstrate a positive-feedback loop whereby gastrin, acting via the CCK2 receptor, increases its own expression. Such an autocrine loop has not previously been reported for any other gastrointestinal hormone. Gastrin promoter activation was dependent on the MAP kinase pathway and did not involve Sp1 binding sites or epidermal growth factor receptor transactivation. As the treatment of gastrointestinal cancer cells with amidated gastrin led to increased expression of non-amidated gastrins, the positive-feedback loop may contribute to the sustained increase in circulating gastrins observed in colorectal cancer patients.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Base Sequence
  • Cell Line, Tumor
  • Colorectal Neoplasms / blood
  • Colorectal Neoplasms / genetics
  • Colorectal Neoplasms / metabolism
  • Feedback, Physiological
  • Gastrins / biosynthesis*
  • Gastrins / blood
  • Gastrins / genetics
  • Gastrins / metabolism*
  • Gastrointestinal Neoplasms / genetics
  • Gastrointestinal Neoplasms / metabolism
  • Gastrointestinal Neoplasms / pathology*
  • Gene Expression Regulation, Neoplastic
  • Genes, Reporter / genetics
  • Humans
  • Luciferases / genetics
  • MAP Kinase Signaling System
  • Molecular Sequence Data
  • Polymerase Chain Reaction
  • Promoter Regions, Genetic / genetics
  • Receptor, Cholecystokinin B / metabolism*
  • Time Factors
  • Transcription, Genetic
  • Transcriptional Activation

Substances

  • Gastrins
  • Receptor, Cholecystokinin B
  • Luciferases