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Impact of Procyanidins from Different Berries on Caspase 8 Activation in Colon Cancer
C. Minker, L. Duban, D. Karas, P. Järvinen, A. Lobstein, CD. Muller,
Language English Country United States
Document type Journal Article, Research Support, Non-U.S. Gov't
NLK
Free Medical Journals
from 2008
PubMed Central
from 2008
Europe PubMed Central
from 2008
ProQuest Central
from 2014-01-01
Open Access Digital Library
from 2008-01-01
Open Access Digital Library
from 2008-01-01
Open Access Digital Library
from 2009-01-01
Medline Complete (EBSCOhost)
from 2011-01-01
Health & Medicine (ProQuest)
from 2014-01-01
Wiley-Blackwell Open Access Titles
from 2008
PubMed
26180579
DOI
10.1155/2015/154164
Knihovny.cz E-resources
- MeSH
- fas Receptor metabolism MeSH
- Apoptosis drug effects MeSH
- Blueberry Plants chemistry metabolism MeSH
- Cell Line MeSH
- Drug Resistance, Neoplasm MeSH
- DNA metabolism MeSH
- Phosphatidylserines metabolism MeSH
- Phosphorylation drug effects MeSH
- DNA Fragmentation drug effects MeSH
- Caspase 3 metabolism MeSH
- Caspase 8 metabolism MeSH
- Caspase 9 metabolism MeSH
- Humans MeSH
- p38 Mitogen-Activated Protein Kinases metabolism MeSH
- Colonic Neoplasms metabolism pathology MeSH
- Fruit chemistry metabolism MeSH
- Proanthocyanidins chemistry isolation & purification toxicity MeSH
- TNF-Related Apoptosis-Inducing Ligand toxicity MeSH
- Plant Extracts chemistry MeSH
- Receptors, TNF-Related Apoptosis-Inducing Ligand metabolism MeSH
- Vaccinium vitis-idaea chemistry metabolism MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
SCOPE: The aim of this work is to identify which proapoptotic pathway is induced in human colon cancer cell lines, in contact with proanthocyanidins extracted from various berries. METHODS AND RESULTS: Proanthocyanidins (Pcys) extracted from 11 berry species are monitored for proapoptotic activities on two related human colon cancer cell lines: SW480-TRAIL-sensitive and SW620-TRAIL-resistant. Apoptosis induction is monitored by cell surface phosphatidylserine (PS) detection. Lowbush blueberry extract triggers the strongest activity. When tested on the human monocytic cell line THP-1, blueberry Pcys are less effective for PS externalisation and DNA fragmentation is absent, highlighting a specificity of apoptosis induction in gut cells. In Pcys-treated gut cell lines, caspase 8 (apoptosis extrinsic pathway) but not caspase 9 (apoptosis intrinsic pathway) is activated after 3 hours through P38 phosphorylation (90 min), emphasizing the potency of lowbush blueberry Pcys to eradicate gut TRAIL-resistant cancer cells. CONCLUSION: We highlight here that berries Pcys, especially lowbush blueberry Pcys, are of putative interest for nutritional chemoprevention of colorectal cancer in view of their apoptosis induction in a human colorectal cancer cell lines.
Merck Millipore Bioscience Division 78180 Saint Quentin en Yvelines France
UMR 7200 CNRS Faculté de Pharmacie 75 route du Rhin 67400 Illkirch France
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