Cis-acting elements required for expression of the nonspecific cross-reacting antigen gene in colorectal carcinoma

Gastroenterology. 1997 Mar;112(3):776-82. doi: 10.1053/gast.1997.v112.pm9041239.

Abstract

Background & aims: The nonspecific cross-reacting antigen (NCA) is a cell adhesion molecule, and the messenger RNA for NCA is overexpressed in 92% of colorectal carcinomas. The aim of this study was to determine the cis-acting elements that may be responsible for the expression of NCA.

Methods: Deletion mutants of the 5' flanking sequence and first intron were ligated into chloramphenicol acetyltransferase expression vectors, transfected into Chinese hamster ovary (CHO), DiFi, and HT-29 human colorectal carcinoma cells, and BxPC-3 and MDAPanc-28 human pancreatic carcinoma cells. The amount of acetylated chloramphenicol was determined to show the presence and activity of cis-acting sequences.

Results: The 5' flanking sequence functions as a promoter in all of cell lines and contains negative regulatory and enhancer sequences. The minimal promoter is active in Chinese hamster ovary and HT-29, though not in MDAPanc-28 cells. The first intron contains a silencer capable of suppressing a heterologous promoter.

Conclusions: The results show cis-acting sequences within and 5' to the NCA gene, which appear to play a role in the expression of this gene in malignant tissues. Some of these sequences function in a cell type-specific manner. Further studies of these elements may provide insight into the mechanisms of the abnormal growth patterns of malignant cells.

Publication types

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

MeSH terms

  • Animals
  • Antigens, Neoplasm / genetics*
  • Base Sequence
  • CHO Cells
  • Cell Adhesion Molecules*
  • Colorectal Neoplasms / genetics*
  • Cricetinae
  • Gene Expression Regulation, Neoplastic*
  • HT29 Cells
  • Humans
  • Introns
  • Membrane Glycoproteins / genetics*
  • Molecular Sequence Data
  • Promoter Regions, Genetic
  • Tumor Cells, Cultured

Substances

  • Antigens, Neoplasm
  • Cell Adhesion Molecules
  • Membrane Glycoproteins