Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 3 de 3
Filter
Add more filters










Database
Language
Publication year range
1.
Anticancer Res ; 38(1): 83-93, 2018 01.
Article in English | MEDLINE | ID: mdl-29277760

ABSTRACT

BACKGROUND/AIM: Due to their unique composition of health-promoting compounds, the consumption of hazelnuts may contribute to the prevention of colon cancer. MATERIALS AND METHODS: Since hazelnuts are often consumed roasted, the impact of different roasting conditions (RC1=140.6°C/25 min, RC2=155.1°C/20 min and RC3=180.4°C/21 min) on chemopreventive effects of in vitro fermented hazelnuts was analyzed in LT97 colon adenoma cells. RESULTS: FS (2.5%) of raw and roasted hazelnuts reduced H2O2-induced DNA damage while 5% FS significantly induced gene expression of SOD2 (3.0-fold) and GSTP1 (2.1-fold). GPx1 mRNA levels were significantly decreased (0.6-fold) by FS (2.5%). The growth of LT97 cells was significantly reduced by hazelnut FS in a time- and dose-dependent manner. Hazelnut FS (5%) increased the numbers of early apoptotic cells (9.6% on average) and caspase-3 activities (6.4-fold on average). CONCLUSION: These results indicate a chemopreventive potential of in vitro fermented hazelnuts which is largely unaffected by the roasting process.


Subject(s)
Adenoma/drug therapy , Anticarcinogenic Agents/pharmacology , Antineoplastic Agents/pharmacology , Colonic Neoplasms/drug therapy , Corylus , Plant Preparations/pharmacology , Adenoma/genetics , Adenoma/prevention & control , Apoptosis/drug effects , Catalase/genetics , Cell Line, Tumor , Cell Proliferation/drug effects , Colonic Neoplasms/genetics , Colonic Neoplasms/prevention & control , Cooking , DNA Damage/drug effects , Glutathione Peroxidase/genetics , Glutathione S-Transferase pi/genetics , Humans , Hydrogen Peroxide/toxicity , Nuts , RNA, Messenger/metabolism , Superoxide Dismutase-1/genetics , Glutathione Peroxidase GPX1
2.
Nutrients ; 9(12)2017 Dec 18.
Article in English | MEDLINE | ID: mdl-29258268

ABSTRACT

Pistachios are rich in health-promoting bioactive compounds such as B vitamins, γ-tocopherol, polyphenols and dietary fiber, which could contribute to the reduction of colon cancer risk in terms of chemoprevention (Fischer, S.; Glei, M. Health-Potential of Nuts. Ernaehrungs Umsch. Int. 2013, 60, 206-215.). Since pistachios are often consumed roasted, the present study aims at investigating the influence of different roasting conditions (RC) on potential chemopreventive effects of pistachios in colon adenoma cells such as growth and apoptosis, genotoxic- and anti-genotoxic effects and modulation of gene expression of detoxifying enzymes (CAT, SOD2, GPx1, and GSTP1). Fermentation supernatants (FS) were obtained from raw and roasted (RC1 = 141 °C/25 min, RC2 = 160 °C/15 min and RC3 = 185 °C/21 min) pistachios after in vitro fermentation. FS of pistachios significantly reduced LT97 cell growth in a time- and dose-dependent manner. Compared to the blank control, pistachio FS (2.5%) led to a significant average reduction of H2O2-induced DNA damage (1.5-fold). Levels of CAT mRNA were significantly increased (1.3-fold, on average for 5% FS). Pistachio FS (5%) significantly increased the number of early apoptotic cells (up to 2.1-fold) and levels of caspase-3 activities (up to 6.9-fold). The present results confirm a chemopreventive potential of pistachios, which is mediated by growth inhibition, induction of apoptosis and anti-genotoxic effects, as well as induction of CAT. These effects remain mostly unaffected by roasting.


Subject(s)
Colonic Neoplasms/prevention & control , Nuts/chemistry , Pistacia/chemistry , Anticarcinogenic Agents/analysis , Antioxidants/analysis , Apoptosis , Catalase/metabolism , Cell Line, Tumor , Cell Proliferation , Colon/cytology , Colon/metabolism , Comet Assay , DNA Damage , Dietary Fiber/analysis , Fermentation , Food Handling , Glutathione Peroxidase/metabolism , Glutathione S-Transferase pi/metabolism , Humans , Lutein/analysis , Polyphenols/analysis , Superoxide Dismutase/metabolism , Vitamin B Complex/analysis , Zeaxanthins/analysis , gamma-Tocopherol/analysis , Glutathione Peroxidase GPX1
3.
Mol Carcinog ; 56(5): 1461-1471, 2017 05.
Article in English | MEDLINE | ID: mdl-27996158

ABSTRACT

Due to their beneficial nutritional profile the consumption of nuts contributes to a healthy diet and might reduce colon cancer risk. To get closer insights into potential mechanisms, the chemopreventive potential of different in vitro fermented nut varieties regarding the modulation of genes involved in detoxification (CAT, SOD2, GSTP1, GPx1) and cell cycle (p21, cyclin D2) as well as proliferation and apoptosis was examined in LT97 colon adenoma and primary epithelial colon cells. Fermentation supernatants (FS) of nuts significantly induced mRNA expression of CAT (up to 4.0-fold), SOD2 (up to 2.5-fold), and GSTP1 (up to 2.3-fold), while GPx1 expression was significantly reduced by all nut FS (0.8 fold on average). Levels of p21 mRNA were significantly enhanced (up to 2.6-fold), whereas all nut FS significantly decreased cyclin D2 expression (0.4-fold on average). In primary epithelial cells, expression of CAT (up to 3.5-fold), GSTP1 (up to 3.0-fold), and GPx1 (up to 3.9-fold) was increased, whereas p21 and cyclin D2 levels were not influenced. Nut FS significantly inhibited growth of LT97 cells and increased levels of early apoptotic cells (8.4% on average) and caspase 3 activity (4.6-fold on average), whereas caspase 3 activity was not modulated in primary colon cells. The differential modulation of genes involved in detoxification and cell cycle together with an inhibition of proliferation and induction of apoptosis in adenoma cells might contribute to chemopreventive effects of nuts regarding colon cancer.


Subject(s)
Adenoma/prevention & control , Anticarcinogenic Agents/pharmacology , Colon/cytology , Colonic Neoplasms/prevention & control , Nuts , Adenoma/genetics , Adenoma/pathology , Apoptosis/drug effects , Cell Line, Tumor , Cell Proliferation/drug effects , Colon/drug effects , Colon/pathology , Colonic Neoplasms/genetics , Colonic Neoplasms/pathology , Epithelial Cells/drug effects , Fermentation , Gene Expression Regulation, Neoplastic/drug effects , Humans
SELECTION OF CITATIONS
SEARCH DETAIL
...