Transforming growth factor-beta 1 stimulates or inhibits cell growth via down- or up-regulation of p21/Waf1

Biochem Biophys Res Commun. 1998 May 29;246(3):873-80. doi: 10.1006/bbrc.1998.8712.

Abstract

Transforming growth factor-beta (TGF-beta) regulates cell proliferation positively or negatively. The mitoinhibition by TGF-beta has been attributed to induction of cyclin-dependent kinase (CDK) inhibitors, such as p15/ Ink4B, p27/Kip1, and p21/Waf1 also known as Cip1 and Sdi1. However, the biological process by which TGF-beta exerts the stimulatory effects on cell growth remains poorly understood. Here we report that TGF-beta 1 stimulates DNA synthesis of IMR-90 human embryonic lung fibroblasts but inhibits that of HuCCT1 human cholangiocarcinoma cells, via down- or up-regulation of p21/Waf1, respectively. TGF-beta 1 markedly suppresses IMR-90 cells to express two different kinds of the p21/Waf1 gene transcription factors, the p53 tumor suppressor and the interferon regulatory factor-1 (IRF-1). This is followed by a marked decrease in expression of p21/Waf1 in a manner consistent with the timing of activation of cyclin E-associated kinase, which normally accompanies the G1-S transition in the cell cycle. Contrarily, TGF-beta 1-induced inhibition of DNA synthesis in HuCCT1 cells is preceded by IRF-1-dependent but p53-independent up-regulation of p21/Waf1 expression followed by inactivation of cyclin E-associated kinase. Thus the cell growth stimulation or inhibition by TGF-beta 1 are mediated by the down- or up-regulation of p21/ Waf1, respectively.

Publication types

  • Comparative Study

MeSH terms

  • CDC2-CDC28 Kinases*
  • Cell Division
  • Cells, Cultured
  • Cholangiocarcinoma / metabolism*
  • Cholangiocarcinoma / pathology
  • Cyclin-Dependent Kinase 2
  • Cyclin-Dependent Kinase Inhibitor p21
  • Cyclin-Dependent Kinases / metabolism
  • Cyclins / biosynthesis*
  • DNA / biosynthesis
  • DNA-Binding Proteins / biosynthesis
  • Down-Regulation*
  • Embryo, Mammalian / cytology
  • Embryo, Mammalian / metabolism
  • Fibroblasts / cytology
  • Fibroblasts / metabolism*
  • Humans
  • Interferon Regulatory Factor-1
  • Lung / cytology
  • Lung / metabolism
  • Phosphoproteins / biosynthesis
  • Protein Serine-Threonine Kinases / metabolism
  • Transforming Growth Factor beta / pharmacology*
  • Tumor Suppressor Protein p53 / biosynthesis
  • Up-Regulation*

Substances

  • CDKN1A protein, human
  • Cyclin-Dependent Kinase Inhibitor p21
  • Cyclins
  • DNA-Binding Proteins
  • IRF1 protein, human
  • Interferon Regulatory Factor-1
  • Phosphoproteins
  • Transforming Growth Factor beta
  • Tumor Suppressor Protein p53
  • DNA
  • Protein Serine-Threonine Kinases
  • CDC2-CDC28 Kinases
  • CDK2 protein, human
  • Cyclin-Dependent Kinase 2
  • Cyclin-Dependent Kinases