Antiproliferative effect of conjugated linoleic acid in caco-2 cells: Involvement of PPARγ and APC/β-catenin pathways
- 作者：Francesca Bozzo ; Claudia Bocca ; Sebastiano Colombatto ; Antonella Miglietta
- 关键词：CLA ; Caco-2 ; Proliferation ; PPARγ ; APC ; β ; -Catenin
- 刊名：Chemico-Biological Interactions
- 出版年：2007
- 期刊代码：6_00092797
- 类别：pha
- 出版时间：30 August 2007
- 卷：169
- 期：2
- 页码：110-121
- 文件大小：1988 K
摘要
Conjugated linoleic acid (CLA), a naturally occurring substance in food sources, occurs as mixtures of positional and geometrical isomers of octadecadienoate (18:2), and may inhibit colon tumorigenesis. It has been hypothesized that CLA can modulate cell proliferation and differentiation through the activation of peroxisome proliferator-activated receptors (PPARs), among which PPARγ is involved in growth inhibition of transformed cells. The aim of the present study was to investigate whether the antiproliferative effects of CLA are mediated by its interaction with PPARγ and APC/β-catenin signalling pathway in human colon cancer cells. In CLA-treated caco-2 cells we found a remarkable increase in the expression of PPARγ, which translocated into the nucleus, while PPARα and β/δ protein levels were not affected. GW259662, a well known PPARγ antagonist, blocked the increase in PPARγ protein rate and abrogated some biological effects of CLA, as it restored the proliferative capability of the cells and ERK1/2 phosphorylation level. We demonstrated that CLA treatment determined the down-regulation of APC and c-myc proteins, but in this case the administration of the antagonist was not able to revert CLA effects. Furthermore, CLA induced a reorganization of E-cadherin and β-catenin, as well as a redistribution of actin and tubulin filaments. Our data suggest that CLA may regulate PPARγ expression by selectively acting as an agonist; however, the discrepancies in PPARγ antagonist efficacy suggest the involvement of other pathways, independent of PPARγ, in CLA antiproliferative activity.