Tumor suppressor and anti-inflammatory actions of PPARγ agonists are mediated via upregulation of PTEN

The PTEN tumor suppressor gene modulates several cellular functions, including cell migration, survival, and proliferation [1] by antagonizing phosphatidylinositol 3-kinase (PI 3-kinase)-mediated signaling cascades. Mechanisms by which the expression of PTEN is regulated are, however, unclear. The l...

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Bibliographic Details
Published in:Current biology 2001-05, Vol.11 (10), p.764-768
Main Authors: Patel, Lisa, Pass, Ian, Coxon, Phil, Downes, C.Peter, Smith, Stephen A., Macphee, Colin H.
Format: Article
Language:English
Subjects:
peroxisome proliferator-activated receptors
PTEN gene
rosiglitazone
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Summary:The PTEN tumor suppressor gene modulates several cellular functions, including cell migration, survival, and proliferation [1] by antagonizing phosphatidylinositol 3-kinase (PI 3-kinase)-mediated signaling cascades. Mechanisms by which the expression of PTEN is regulated are, however, unclear. The ligand-activated nuclear receptor peroxisome proliferator-activated receptor γ (PPARγ) [2] has been shown to regulate differentiation and/or cell growth in a number of cell types [3, 4, 5], which has led to the suggestion that PPARγ, like PTEN [1, 6], could act as a tumor suppressor. PPARγ has also been implicated in anti-inflammatory responses [7, 8], although downstream mediators of these effects are not well defined. Here, we show that the activation of PPARγ by its selective ligand, rosiglitazone, upregulates PTEN expression in human macrophages, Caco2 colorectal cancer cells, and MCF7 breast cancer cells. This upregulation correlated with decreased PI 3-kinase activity as measured by reduced phosphorylation of protein kinase B. One consequence of this was that rosiglitazone treatment reduced the proliferation rate of Caco2 and MCF7 cells. Antisense-mediated disruption of PPARγ expression prevented the upregulation of PTEN that normally accompanies monocyte differentiation and reduced the proportion of macrophages undergoing apoptosis, while electrophoretic mobility shift assays showed that PPARγ is able to bind two response elements in the genomic sequence upstream of PTEN. Our results demonstrate a role for PPARγ in regulating PI 3-kinase signaling by modulating PTEN expression in inflammatory and tumor-derived cells.
ISSN:0960-9822
1879-0445
DOI:10.1016/S0960-9822(01)00225-1