CD44H plays an important role in peritoneal dissemination of scirrhous gastric cancer cells

Jpn J Cancer Res. 1996 Dec;87(12):1235-44. doi: 10.1111/j.1349-7006.1996.tb03138.x.


The role of the adhesion molecule CD44H in the peritoneal adhesion and invasion of cancer cells was assessed using cell lines with low and high peritoneal seeding ability, OCUM-2M (2M) and OCUM-2MD3 (2MD3), respectively. The in vitro binding ability to peritoneal components (mesothelial cells, fibronectin and type I collagen) and invasive ability of 2MD3 cells were higher than those of 2M cells. The expression level of CD44H on 2MD3 cells was higher than that on 2M cells as determined by western blot analysis and flow cytometry. The adhesiveness of 2MD3 cells to hyaluronic acid, which is expressed on the surfaces of mesothelial cells, was greater than that of 2M cells. The binding ability of 2MD3 cells to mesothelial cells was inhibited in the presence of anti-CD44H monoclonal antibody, but that of 2M cells was not. These results suggested that the 2MD3 cell binding to mesothelial cells is regulated by the CD44-hyaluronic acid dependent system. The in vitro binding to submesothelial components and the invasiveness of 2MD3 cells were also inhibited in the presence of anti-CD44H antiody. The in vivo inoculation of 2MD3 cells treated with an anti-CD44H antibody resulted in a significiant prolongation of survival time as compared with control mice that were inoculated with 2MD3 cells alone. In conclusion, CD44H was associated with attachment not only to hyaluronic acid on mesothelial cells, but also to peritoneal stromal components. Thus, CD44H may play an important role in cancer cell binding and invasion in the peritoneal dissemination of scirrhous gastric cancer cells.

MeSH terms

  • Adenocarcinoma, Scirrhous / chemistry
  • Adenocarcinoma, Scirrhous / pathology*
  • Animals
  • Antibodies / metabolism
  • Blotting, Western
  • Cell Adhesion
  • Epithelium / metabolism
  • Extracellular Matrix / metabolism
  • Humans
  • Hyaluronan Receptors / analysis
  • Hyaluronan Receptors / physiology*
  • Mice
  • Neoplasm Invasiveness
  • Peritoneum / pathology*
  • Stomach Neoplasms / chemistry
  • Stomach Neoplasms / pathology*
  • Tumor Cells, Cultured


  • Antibodies
  • Hyaluronan Receptors