Peroxisome proliferator-activated receptor-γ ligands for the treatment of breast cancer
- 1 June 2005
- journal article
- review article
- Published by Taylor & Francis in Expert Opinion on Investigational Drugs
- Vol. 14 (6) , 557-568
- https://doi.org/10.1517/13543784.14.6.557
Abstract
Pioglitazone and rosiglitazone are thiazolidinediones used for the treatment of Type 2 diabetes mellitus. They modulate glucose and fat metabolism, mainly by binding to the nuclear hormone receptor peroxisome proliferator-activated receptor (PPAR)-γ. PPAR-γ signalling is involved in a number of other disease conditions including cancer. In breast cancer cells, PPAR-γ ligands inhibit proliferation and induce apoptosis both in vitro and in vivo. PPAR-γ ligands also inhibit tumour angiogenesis and invasion. The only published clinical trial using a PPAR-γ ligand in patients with metastatic breast cancer failed to show any clinical benefits. The mechanism of action of the thiazolidinediones in breast cancer cells is not fully understood but involves interactions with other nuclear hormone receptors, transcriptional co-activators and repressors as well as PPAR-γ-independent effects. A better understanding of these mechanisms will be needed before PPAR-γ ligands may be useful in the treatment of breast cancer p...Keywords
This publication has 101 references indexed in Scilit:
- GW9662, a potent antagonist of PPARγ, inhibits growth of breast tumour cells and promotes the anticancer effects of the PPARγ agonist rosiglitazone, independently of PPARγ activationBritish Journal of Pharmacology, 2004
- Antineoplastic effects of peroxisome proliferatoractivated receptor γ agonistsThe Lancet Oncology, 2004
- Sirt1 promotes fat mobilization in white adipocytes by repressing PPAR-γNature, 2004
- PPARγ signaling exacerbates mammary gland tumor developmentGenes & Development, 2004
- Metabolic and Additional Vascular Effects of ThiazolidinedionesDrugs, 2002
- Troglitazone Inhibits Growth of MCF-7 Breast Carcinoma Cells by Targeting G1 Cell Cycle RegulatorsBiochemical and Biophysical Research Communications, 2001
- Terminal Differentiation of Human Breast Cancer through PPARγMolecular Cell, 1998
- The Antidiabetic Agent Thiazolidinedione Stimulates the Interaction between PPARγ and CBPBiochemical and Biophysical Research Communications, 1997
- Transdifferentiation of myoblasts by the adipogenic transcription factors PPAR gamma and C/EBP alpha.Proceedings of the National Academy of Sciences, 1995
- Stimulation of adipogenesis in fibroblasts by PPARγ2, a lipid-activated transcription factorCell, 1994