The effect of PPARgamma ligands on the proliferation and apoptosis of human melanoma cells.

Abstract

The peroxisome proliferator-activated receptor gamma (PPARgamma) is a member of the nuclear receptor family of ligand-activated transcription factors. PPARgamma ligands have been shown to inhibit the growth of cells from different cancer lineages. This study was designed to evaluate the effects of PPARgamma receptor activation in human melanoma cell lines. The effects of its expression and activation on cell proliferation and apoptosis in human melanoma cell lines (early stage cancer [WM35] and metastatic tumour [A375]) were investigated. Reverse transcription-polymerase chain reaction and Western blot analysis showed that both human melanoma cell lines expressed PPARgamma mRNA and protein. Treatment of cells transfected with the luciferase gene ligated to PPAR response element constructed promoter showed that ciglitazone and prostaglandin J2 (PGJ2), selective ligands for PPARgamma, increased the luciferase activity, proving the induction of the PPARgamma reporter gene. Ciglitazone and PGJ2 inhibited melanoma cell proliferation in a dose-dependent manner. Analysis of the cellular morphology and apoptosis assayed by fluorescence microscopy after incubation of A375 cells with 10 micro M ciglitazone for 24 h indicated that this ligand not only inhibited cell proliferation but also induced apoptosis.

• Authors: Wojciech Placha, Dorota Gil, Aldona Dembińska-Kieć, Piotr Laidler
• Journal: Melanoma research (Melanoma Res) Vol. 13 Issue 5 Pg. 447-56 (Oct 2003) ISSN: 0960-8931 [Print] England
• PMID: 14512786 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• Antineoplastic Agents
• Hypoglycemic Agents
• Ligands
• Receptors, Cytoplasmic and Nuclear
• Thiazolidinediones
• Transcription Factors
• 9-deoxy-delta-9-prostaglandin D2
• DNA
• Luciferases
• Prostaglandin D2
• ciglitazone

Topics

• Antineoplastic Agents (pharmacology)
• Apoptosis
• Blotting, Western
• Cell Division
• Cell Line, Tumor
• DNA (chemistry)
• Dose-Response Relationship, Drug
• Humans
• Hypoglycemic Agents (pharmacology)
• Ligands
• Luciferases (metabolism)
• Melanoma (pathology)
• Microscopy, Fluorescence
• Promoter Regions, Genetic
• Prostaglandin D2 (analogs & derivatives, pharmacology)
• Receptors, Cytoplasmic and Nuclear (metabolism)
• Reverse Transcriptase Polymerase Chain Reaction
• Thiazolidinediones (pharmacology)
• Time Factors
• Transcription Factors (metabolism)