J Korean Surg Soc.  1998 Jun;54(Suppl):966-974.

Expression of CD44H in Gastric Cancer Cells and Binding Ability to the Peritoneal Mesothelium

Affiliations
  • 1Departments of Surgery and 1Internal Medicine, Catholic University Medical College.

Abstract

Understanding of the adhesion molecules involved in the interaction of gastric cancer cells with peritoneal mesothelial cells (PMC) might provide a useful strategy for interfering with cancer cell implantation to the peritoneum. Since CD44H is a major cell surface receptor for hyaluronate (HA), it may play an important role in mediating cancer cell adhesion to PMC through recognition of mesothelium associated HA. The purpose of the present study was to define the functional significance of CD44H in peritoneal metastasis of gastric cancer cells by using quantitative assays for measuring the adhesion ability to PMC in vitro. CD44 expression in gastric cancer cell lines SNU-1, -5, and -16 were examined by reverse transcription-polymerase chain reaction (RT-PCR) and Western blot analysis. CD44H was expressed in SNU-5 and -16 whereas no significant level of CD44H was expressed in SNU-1. SNU-16 expressed additional high-molecular-weight CD44 isoforms. In the adhesion assay with HA coated microtiter wells, SNU-5 and -16 demonstrated high affinity for HA, with values of 64.6+/-10.5% and 91.1+/-8.8%, respectively. SNU-1 demonstrated no significant binding affinity for HA (p<0.05). For the in vitro binding assay, we used a confluent monolayer of PMC. 2.5x10(4) and 5x10(4) gastric cancer cells labelled with 51 Cr were inoculated into microtiter wells and allowed to adhere for 2 hr. After washing of the unattached cancer cells, adherent cells were lysed with 0.1 N NaOH and the radioactivity was measured in the lysates. SNU-5 and -16 bound to PMC, to the extent of 10.0+/-1.0%, 14.6+/-1.8% and 22.9+/-2.0%, 23.7+/-3.6%, respectively. In contrast, SNU-1 demonstrated lower binding ability(6.4+/- 0.5%, 6.7+/-1.3%, respectively) to PMC. In conclusion, CD44H is at least partly involved in gastric cancer cell binding to PMC, which mediates an important first step of peritoneal implantation.

Keyword

Stomach cancer; CD44; Cell adhesion molecule; Peritoneal metastasis

MeSH Terms

Blotting, Western
Cell Adhesion
Cell Line
Epithelium*
Negotiating
Neoplasm Metastasis
Peritoneum
Protein Isoforms
Radioactivity
Stomach Neoplasms*
Protein Isoforms
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