Transformation of revertant murine cells by 5-azacytidine results in rapid inhibition of lysyl oxidase expression

Acta Microbiol Immunol Hung. 2005;52(3-4):433-42. doi: 10.1556/AMicr.52.2005.3-4.13.

Abstract

Lysyl oxidase (LO) is synthesized intracellularly as a proenzyme that is secreted and then processed extracellularly to a mature form. LO is expressed in NIH3T3 cells, but only very low levels are observed after NIH 3T3 is transformed by c-H-ras or one of several other oncogenes. LO functions as a tumor suppressor. Treatment of ras-transformed cells with interferon-alpha with or without retinoic acid results in their persistent reversion to a non-transformed state that is dependent on the restoration of LO expression. When such revertant cells are treated with 5-azacytidine (5-azaC), they undergo rapid morphological retransformation. Within one passage after addition of 5-azaC, there was a down regulation of LO mRNA and proenzyme protein. These data suggest a direct relationship between the transformed state and LO expression.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Azacitidine / pharmacology*
  • Cell Line, Transformed
  • Cell Transformation, Neoplastic*
  • Gene Expression Regulation, Neoplastic*
  • Genes, ras / genetics
  • Genes, ras / physiology
  • Mice
  • NIH 3T3 Cells
  • Protein-Lysine 6-Oxidase / genetics*
  • Protein-Lysine 6-Oxidase / metabolism*
  • Time Factors

Substances

  • Protein-Lysine 6-Oxidase
  • Azacitidine