Cell adhesion molecules of the immunoglobulin supergene family and their role in malignant transformation and progression to metastatic disease

Cancer Metastasis Rev. 1991 May;10(1):11-22. doi: 10.1007/BF00046840.

Abstract

Cell adhesion molecules (CAMs) of the immunoglobulin supergene family may play important roles in tumorigenesis and the development of metastatic disease. In a variety of human malignancies, tumor progression has been observed to be associated with changes in CAM expression. An early event in colorectal tumorigenesis appears to be the down regulation of a normally expressed CAM, DCC. Over-expression of a second CAM, carcinoembryonic antigen, is associated with colorectal tumors which have a high risk for metastasis development. Several tumors, including Wilms tumors and neuroblastoma, have been found to express a developmentally regulated form of NCAM which inhibits a variety of cell-cell interactions. Malignant cells not only show aberrations in the expression of their CAMS and thus their normal cell-cell interactions, but establish new adhesive interactions. The development of metastatic potential in cutaneous melanoma is associated with the de novo expression of two CAMs, one of which is ICAM-1, a molecule mediating adhesion between the tumor cells and leukocytes.

Publication types

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

MeSH terms

  • Amino Acid Sequence
  • Antigens, CD*
  • CD146 Antigen
  • Carcinoembryonic Antigen / physiology
  • Cell Adhesion
  • Cell Adhesion Molecules / physiology*
  • Cell Adhesion Molecules, Neuronal / physiology
  • Cell Transformation, Neoplastic / pathology*
  • Chromosomes, Human, Pair 18
  • Colorectal Neoplasms / genetics
  • Colorectal Neoplasms / pathology
  • Gene Expression Regulation, Neoplastic
  • Genes, Immunoglobulin / physiology
  • Humans
  • Intercellular Adhesion Molecule-1
  • Melanoma / pathology
  • Membrane Glycoproteins / physiology
  • Molecular Sequence Data
  • Neoplasm Metastasis / pathology*
  • Neural Cell Adhesion Molecules*

Substances

  • Antigens, CD
  • CD146 Antigen
  • Carcinoembryonic Antigen
  • Cell Adhesion Molecules
  • Cell Adhesion Molecules, Neuronal
  • Membrane Glycoproteins
  • Neural Cell Adhesion Molecules
  • Intercellular Adhesion Molecule-1