The cytoplasmic domain of C-CAM1 tumor suppressor is necessary and sufficient for suppressing the tumorigenicity of prostate cancer cells

Biochem Biophys Res Commun. 1999 Oct 5;263(3):797-803. doi: 10.1006/bbrc.1999.1443.

Abstract

We have previously shown that C-CAM1 cell adhesion molecule can suppress the growth of prostate cancer cells in vivo. In this study, we determined the minimal domain of C-CAM1 that is required for its tumor-suppressive activity. DU145 prostate cancer cells were infected with recombinant adenoviruses containing various C-CAM1 mutant genes, and the effects of the mutant C-CAM1 proteins on the growth of DU145 cells were assessed in a nude-mice xenograft model. Deletion of C-CAM1's cytoplasmic domain, which is not required for its adhesion activity, abolished the growth-suppressive activity, whereas deletion of the adhesion domain did not. This observation suggests that C-CAM1's extracellular domain may be not essential for its tumor suppressive activity. Indeed, we found that expression of the C-CAM1 cytoplasmic domain alone led to growth suppression of DU145 cells. These results suggest that the cytoplasmic domain of C-CAM1 is necessary and sufficient for its growth-suppressive function.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adenosine Triphosphatases / chemistry*
  • Adenosine Triphosphatases / genetics
  • Adenosine Triphosphatases / physiology*
  • Adenoviridae
  • Animals
  • Antigens, CD
  • Carcinoembryonic Antigen
  • Cell Adhesion
  • Cell Adhesion Molecules / chemistry*
  • Cell Adhesion Molecules / genetics
  • Cell Adhesion Molecules / physiology*
  • Cell Aggregation
  • Cell Division
  • Cloning, Molecular
  • Cytoplasm / metabolism
  • Genetic Vectors
  • Glycoproteins
  • Humans
  • Male
  • Mice
  • Mice, Nude
  • Mutagenesis, Site-Directed
  • Prostatic Neoplasms / pathology*
  • Prostatic Neoplasms / physiopathology*
  • Recombinant Proteins / chemistry
  • Recombinant Proteins / metabolism
  • Transfection

Substances

  • Antigens, CD
  • CD66 antigens
  • Carcinoembryonic Antigen
  • Ceacam1 protein, mouse
  • Ceacam2 protein, mouse
  • Cell Adhesion Molecules
  • Glycoproteins
  • Recombinant Proteins
  • Adenosine Triphosphatases