| Abstract | Dietary polyphenols have been associated with reduced risk of chronic diseases, but the precise molecular mechanisms of protection remain unclear. This work was aimed at studying the effect of (-)-epicatechin (EC) and chlorogenic acid (CGA) on the regulation of apoptotic and survival/proliferation pathways in a human hepatoma cell line (HepG2). EC or CGA treatment for 18 h had a slight effect on cell viability and decreased reactive oxygen species formation, and EC alone promoted cell proliferation, whereas CGA increased glutathione levels. Phenols neither induced the caspase cascade for apoptosis nor affected expression levels of Bcl-xL or Bax. A sustained activation of the major survival signals AKT/PI-3-kinase and ERK was shown in EC-treated cells, rather than in CGA-exposed cells. These data suggest that EC and CGA have no effect on apoptosis and enhance the intrinsic cellular tolerance against oxidative insults either by activating survival/proliferation pathways or by increasing antioxidant potential in HepG2. |
| Authors | Ana Belén Granado-Serrano, María Angeles Martín, María Izquierdo-Pulido, Luis Goya, Laura Bravo, Sonia Ramos
(Affiliation: Department of Metabolism and Nutrition, Instituto del Frío, Consejo Superior de Investigaciones Científicas, José Antonio Novais 10, Ciudad Universitaria, 28040 Madrid, Spain.)
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| Journal | Journal of agricultural and food chemistry
(J Agric Food Chem)
Vol. 55
Issue 5
Pg. 2020-7
(Mar 7 2007)
ISSN: 0021-8561 United States |
| PMID | 17286412
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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| Chemical References |
- Reactive Oxygen Species
- Catechin
- Chlorogenic Acid
- 1-Phosphatidylinositol 3-Kinase
- Extracellular Signal-Regulated MAP Kinases
- Proto-Oncogene Proteins c-akt
|
| Topics |
- 1-Phosphatidylinositol 3-Kinase
(metabolism)
- Apoptosis
(drug effects)
- Carcinoma, Hepatocellular
- Catechin
(pharmacology)
- Cell Division
(drug effects)
- Cell Line, Tumor
- Cell Survival
(drug effects)
- Chlorogenic Acid
(pharmacology)
- Extracellular Signal-Regulated MAP Kinases
(metabolism)
- Humans
- Liver Neoplasms
- Phosphorylation
- Proto-Oncogene Proteins c-akt
(metabolism)
- Reactive Oxygen Species
(metabolism)
|