Restoration of RUNX3 enhances transforming growth factor-beta-dependent p21 expression in a biliary tract cancer cell line

Cancer Sci. 2007 Jun;98(6):838-43. doi: 10.1111/j.1349-7006.2007.00460.x.

Abstract

RUNX3 is a candidate tumor suppressor gene localized in 1p36, a region commonly inactivated by deletion and methylation in various human tumors. To elucidate the role of RUNX3 in transforming growth factor (TGF)-beta signaling in biliary tract cancer, we transfected Mz-ChA-2 cells, which do not express RUNX3 but have intact TGF-beta type II receptor and SMAD4 genes, with the RUNX3 expression plasmid pcDNA3.1/RUNX3 or with the vector pcDNA3.1 as a control. Four Mz-ChA-2/RUNX3 clones and one control clone were obtained. Although TGF-beta1 only slightly inhibited growth of the control cells, growth inhibition and TGF-beta-dependent G(1) arrest were significantly enhanced in the RUNX3-transfected clones. None of the clones, however, exhibited apoptosis. The slightly increased TGF-beta1-induced p21 expression in the control clone was strongly enhanced in the RUNX3-transfected clones, and was accompanied by augmented decreases in the expression of cyclins D1 and E. When RUNX3 small interfering RNA was added, TGF-beta-dependent induction of p21 was reduced in the RUNX3-transfected clones. Xenografts of the clones in nude mice demonstrated that tumorigenicity was significantly decreased in the RUNX3-transfected clones in inverse proportion to the expression levels of RUNX3. Based on these results, RUNX3 is involved in TGF-beta-induced expression of p21 and the resulting induction of TGF-beta-dependent G(1) arrest.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biliary Tract Neoplasms / metabolism*
  • Cell Cycle
  • Cell Cycle Proteins / metabolism
  • Cell Line, Tumor
  • Core Binding Factor Alpha 3 Subunit / genetics
  • Core Binding Factor Alpha 3 Subunit / physiology*
  • Cyclin D1 / metabolism
  • Forkhead Box Protein O3
  • Forkhead Transcription Factors / metabolism
  • Gene Expression
  • Humans
  • Proto-Oncogene Proteins p21(ras) / metabolism*
  • Signal Transduction
  • Transfection
  • Transforming Growth Factor beta / pharmacology*
  • Transforming Growth Factor beta1 / pharmacology

Substances

  • Cell Cycle Proteins
  • Core Binding Factor Alpha 3 Subunit
  • FOXO3 protein, human
  • Forkhead Box Protein O3
  • Forkhead Transcription Factors
  • Runx3 protein, human
  • Transforming Growth Factor beta
  • Transforming Growth Factor beta1
  • Cyclin D1
  • Proto-Oncogene Proteins p21(ras)