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Apoptosis-inducing factor and caspase-dependent apoptotic pathways triggered by different grape seed extracts on human colon cancer cell line Caco-2

Authors :
Donato Antonacci
Gabriella Pasqua
Sara Proietti
Alessia Pasqualato
Pierpaolo Coluccia
Anna Rita Santamaria
Aldo Laganà
Alessandra Cucina
Alessandro Giuliani
Mariano Bizzarri
Fabrizio D'Anselmi
Simona Dinicola
Source :
British Journal of Nutrition. 104:824-832
Publication Year :
2010
Publisher :
Cambridge University Press (CUP), 2010.

Abstract

Consumption of grape seed extract (GSE) is widely marketed as a dietary supplement and is considered safe for human health. Nevertheless, theanalytical composition of GSE from different grape cultivars, growing in special agronomic constraints, differs greatly in flavan-3-ols content.The major concern with GSE studies is a lack of availability of uniformly standardised preparations, which raises an important question whetherdifferent GSE samples have comparable activity and trigger the same mechanisms of action on a given biological system. Therefore, it is temptingto speculate that GSE, obtained from different cultivars, could exert differentiated anticancer effects. The focus of the present study is to determinethe selective biological efficacy of GSE obtained from three different sources on the human colon cancer cell line Caco-2. Irrespective of its source,high doses of GSE induced a significant inhibition on Caco-2 cell growth. Moreover, apoptosis was enhanced through both caspase-dependent andcaspase-independent mechanisms, leading to an early apoptosis-inducing factor release and, further, to a dramatic increase in caspase 7 and 3activity. However, a significant difference in apoptotic rates induced by the three grape sources clearly emerged when treating cancer cellswith low and intermediate GSE concentrations (25 and 50mg/ml).Grape seed extracts: Apoptosis-inducing factor: Apoptosis: Flavan-3-ols

Details

ISSN :
14752662 and 00071145
Volume :
104
Database :
OpenAIRE
Journal :
British Journal of Nutrition
Accession number :
edsair.doi.dedup.....0fb0a14691eb8b345db82c7f8fc66b51