Cell CAM 105 isoform RNA expression is differentially regulated during rat liver regeneration and carcinogenesis

Nancy L. Thompson, Sue Hwa Lin, Marilyn A. Panzica, Douglas C. Hixson

Research output: Contribution to journalArticlepeer-review

20 Scopus citations

Abstract

Cell CAM 105 (C-CAM) is a member of the carcinoembryonic antigen family and has been characterized as a rat hepatocyte cell-cell adhesion molecule via antibody activity. Two isoforms have been cloned and differ primarily in the length of the cytoplasmic domain. Despite extensive structural studies, little is known about their function and regulation in vivo. We have examined C-CAM expression during rat liver regeneration and hepatocarcinogenesis. Steady-state C-CAM RNA varied less than 3-fold during regeneration with subtle changes in the isoform ratio both before and after hepatocyte division. In liver tumors and transformed cells derived from tumors, however, large-scale decreases were observed in C-CAM RNA with wide variations in isoform ratios. In general, RNA decreases were reflected at the protein level. Our data suggest whereas down-regulation and alterations in C-CAM isoform ratio are transient during regulated liver growth, they are permanent in malignancy and may modulate hepatocyte adhesion.

Original languageEnglish (US)
Pages (from-to)209-220
Number of pages12
JournalPathobiology
Volume62
Issue number4
DOIs
StatePublished - 1994

Keywords

  • Cell CAM 105
  • Cell adhesion
  • Hepatocarcinogenesis
  • Liver regeneration
  • Rat liver

ASJC Scopus subject areas

  • Pathology and Forensic Medicine
  • Molecular Biology
  • Cell Biology

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