Transforming growth factor-beta1 coregulates mRNA expression of aryl hydrocarbon receptor and cell-cycle-regulating genes in human cancer cell lines

Biochem Biophys Res Commun. 1997 Dec 8;241(1):86-91. doi: 10.1006/bbrc.1997.7773.

Abstract

Transforming growth factor (TGF)-beta1 down-regulates mRNA expression of the aryl hydrocarbon receptor (AhR) and of AhR-inducible genes in A549 cells. Here, we describe a dose-dependent inhibition of 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD)-induced cytochrome P450 (CYP) 1A1, CYP1B1 and NADPH-quinone-oxidoreductase (NMO-1) mRNA expression as well as TCDD-induced 7-ethoxyresorufin-O-deethylase (EROD) activity in MDA-MB 231 cells. The AhR mRNA expression was not affected by TGF-beta1. TGF-beta-responsiveness was investigated by examining the effect on the expression of responsive genes. While TGF-beta1 up-regulates mRNA expression of TGF-beta1 and TIEG (TGF-beta-inducible early gene) as well as luciferase activity of a responsive reporter plasmid in both cell lines, a down-regulation of c-myc and cyclin A mRNA expression was only found in A549 cells. Furthermore, TGF-beta1 inhibits only cell proliferation of A549 but not of MDA-MB 231 cells. The results show a coregulation of mRNA expression of AhR and cell-cycle regulating genes, and further indicate that the AhR may be involved in regulation of cell proliferation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aryl Hydrocarbon Hydroxylases*
  • Breast Neoplasms
  • Cell Cycle / drug effects
  • Cell Cycle / genetics*
  • Cyclin A / biosynthesis*
  • Cytochrome P-450 CYP1A1 / biosynthesis
  • Cytochrome P-450 CYP1B1
  • Cytochrome P-450 Enzyme System / biosynthesis*
  • Female
  • Gene Expression Regulation, Neoplastic / drug effects*
  • Humans
  • Luciferases / biosynthesis
  • Lung Neoplasms
  • NAD(P)H Dehydrogenase (Quinone) / biosynthesis
  • Polychlorinated Dibenzodioxins / pharmacology
  • RNA, Messenger / biosynthesis
  • Receptors, Aryl Hydrocarbon / biosynthesis*
  • Recombinant Fusion Proteins / biosynthesis
  • Transcription, Genetic / drug effects*
  • Transfection
  • Transforming Growth Factor beta / pharmacology*
  • Tumor Cells, Cultured

Substances

  • Cyclin A
  • Polychlorinated Dibenzodioxins
  • RNA, Messenger
  • Receptors, Aryl Hydrocarbon
  • Recombinant Fusion Proteins
  • Transforming Growth Factor beta
  • Cytochrome P-450 Enzyme System
  • Luciferases
  • Aryl Hydrocarbon Hydroxylases
  • CYP1B1 protein, human
  • Cytochrome P-450 CYP1A1
  • Cytochrome P-450 CYP1B1
  • NAD(P)H Dehydrogenase (Quinone)