Peroxisome proliferator-activated receptor γ-dependent activation of p21 in Panc-28 pancreatic cancer cells involves Sp1 and Sp4 proteins

Jun Hong, Ismael Samudio, Shengxi Liu, Maen Abdelrahim, Stephen Safe

Research output: Contribution to journalArticle

70 Scopus citations

Abstract

1,1-Bis(3′-indolyl)-1-(p-trifluoromethylphenyl)methane (DIM-C-pPhCF3) and troglitazene activate peroxisome proliferator-activated receptor γ (PPARγ) in Panc-28 pancreatic cancer cells and also inhibit cell proliferation. DIM-C-pPhCF3 was more active than troglitazone and was used as a model to investigate the mechanism of PPARγ-dependent inhibition of Panc-28 cell growth. DIM-C-pPhCP3 significantly inhibited G0/G 1→S phase progression, as determined by FACS analysis, and this was associated with decreased retinoblastoma protein phosphorylation and increased p21 protein and mRNA expression, but no change in p27 or cyclin D1. PPARγ antagonists blocked DIM-C-pPhCF3-induced growth inhibition and induction of p21 protein, and similar inhibitory effects were observed in Panc-28 cells transfected with a construct (pWWP) containing a -2325 to +8 p21 promoter insert. Deletion analysis of the p21 promoter indicated that PPARγ-dependent activation of p21 promoter constructs by DIM-C-pPhCF 3 required GC-rich sites 3 and 4 in the proximal region (-124 to -60) of the p21 promoter. The results of RNA interference and protein expression/DNA binding assays suggest that DIM-C-pPhCF3 induced p21 expression through a novel mechanism that involves PPARγ interactions with both Sp1 and Sp4 proteins bound to the proximal GC-rich region of the p21 promoter.

Original languageEnglish (US)
Pages (from-to)5774-5785
Number of pages12
JournalEndocrinology
Volume145
Issue number12
DOIs
StatePublished - Dec 2004

ASJC Scopus subject areas

  • Endocrinology

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