Regulation of egr-1 gene expression by retinoic acid in a human growth factor-dependent cell line

Int J Hematol. 1996 Jun;63(4):303-9. doi: 10.1016/0925-5710(96)00451-3.

Abstract

Retinoic acid (RA) has profound suppressive effects on growth and survival of human growth factor-dependent cell line, M07e. Treatment of M07e cells by RA reduced expression of egr-1 gene, while the levels of c-myc gene expression remained similar. Suppression of egr-1 gene expression by RA was dosage-dependent and reached maximum at 4 h after RA addition. The decay of egr-1 mRNA was similar in M07e cells treated with or without RA. The transcriptional activity of the promoter region up to -600 or -480 bp upstream of the egr-1 gene was greatly reduced by RA treatment. These data suggest that biological effects of RA on hematopoietic cells may, in part, be mediated by transcriptional suppression of egr-1 gene through its promoter region within -480 bp.

Publication types

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

MeSH terms

  • DNA-Binding Proteins / biosynthesis*
  • DNA-Binding Proteins / genetics
  • Early Growth Response Protein 1
  • Gene Expression Regulation, Leukemic / drug effects*
  • Genes, Immediate-Early / drug effects*
  • Granulocyte-Macrophage Colony-Stimulating Factor / pharmacology*
  • Humans
  • Immediate-Early Proteins / biosynthesis*
  • Immediate-Early Proteins / genetics
  • Leukemia, Megakaryoblastic, Acute / pathology
  • Megakaryocytes / drug effects*
  • Megakaryocytes / metabolism
  • Megakaryocytes / pathology
  • Neoplasm Proteins / biosynthesis*
  • Neoplasm Proteins / genetics
  • Promoter Regions, Genetic / drug effects
  • Proto-Oncogene Proteins c-myc / biosynthesis
  • Proto-Oncogene Proteins c-myc / genetics
  • RNA, Messenger / metabolism
  • RNA, Neoplasm / genetics
  • Recombinant Proteins / pharmacology
  • Stem Cell Factor / pharmacology
  • Transcription Factors / biosynthesis*
  • Transcription Factors / genetics
  • Transcription, Genetic / drug effects
  • Tretinoin / pharmacology*
  • Tumor Cells, Cultured

Substances

  • DNA-Binding Proteins
  • EGR1 protein, human
  • Early Growth Response Protein 1
  • Immediate-Early Proteins
  • Neoplasm Proteins
  • Proto-Oncogene Proteins c-myc
  • RNA, Messenger
  • RNA, Neoplasm
  • Recombinant Proteins
  • Stem Cell Factor
  • Transcription Factors
  • Tretinoin
  • Granulocyte-Macrophage Colony-Stimulating Factor