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1.
Sci Rep ; 7: 45951, 2017 04 05.
Article in English | MEDLINE | ID: mdl-28378765

ABSTRACT

Colon cancer is one of the most common cancers. In this study, we isolated a lignan [(-)-(2R,3R)-1,4-O-diferuloylsecoisolariciresinol, DFS] from Alnus japonica (Betulaceae) and investigated its biological activity and mechanism of action on colon cancer. DFS reduced the viability of colon cancer cells and induced cell cycle arrest. DFS also suppressed ß-catenin nuclear translocation and ß-catenin target gene expression through a reduction in FoxM1 protein. To assess the mechanism of the action of DFS, we investigated the effect of DFS on endogenous and exogenous FoxM1 protein degradation in colon cancer cells. DFS-induced FoxM1 protein degradation was suppressed by lysosomal inhibitors, chloroquine and bafilomycin A1, but not by knock-down of proteasomal proteins. The mechanism of DFS for FoxM1 degradation is lysosomal dependent, which was not reported before. Furthermore, we found that FoxM1 degradation was partially lysosomal-dependent under normal conditions. These observations indicate that DFS from A. japonica suppresses colon cancer cell proliferation by reducing ß-catenin nuclear translocation. DFS induces lysosomal-dependent FoxM1 protein degradation. This is the first report on the lysosomal degradation of FoxM1 by a small molecule. DFS may be useful in treating cancers that feature the elevated expression of FoxM1.


Subject(s)
Forkhead Box Protein M1/metabolism , Lignans/pharmacology , Lysosomes/metabolism , beta Catenin/metabolism , Active Transport, Cell Nucleus/drug effects , Alnus/chemistry , Animals , Cell Line , Cell Line, Tumor , Cell Proliferation/drug effects , Cell Proliferation/genetics , Cells, Cultured , Forkhead Box Protein M1/genetics , Gene Expression Regulation, Neoplastic/drug effects , HCT116 Cells , HEK293 Cells , Humans , Lignans/chemistry , Mice, Inbred C57BL , Molecular Structure , Proteolysis/drug effects , beta Catenin/genetics
2.
Ecol Food Nutr ; 52(3): 223-38, 2013.
Article in English | MEDLINE | ID: mdl-23621487

ABSTRACT

Pigs' feet are traditionally consumed by Korean women to increase milk production during lactation. In this study, we evaluated the perceived effectiveness and safety of consuming pigs' feet. Parous women were recruited to complete survey questionnaires in South Korea. Of the 516 respondents, 188 (36%) claimed they consumed pigs' feet. One-hundred twenty women (64%) who consumed pigs' feet reported experiencing an increase in breast milk production. Seventy-three (61%) women from this same group exclusively breastfed. In contrast, 16 (25%) of 65 respondents who did not embrace the same purported effect of pigs' feet indicated that they solely breastfed. Ninety-eight (82%) respondents who consumed pigs' feet and reported galactagoguic effects would recommend its use. Study findings reveal that the majority of women who consume pigs' feet believe in its milk-promoting effects. The results of this study suggest that further investigation of the galactagoguic effects of pigs' feet via conduction of an experimental study is warranted.


Subject(s)
Breast Feeding , Culture , Feeding Behavior , Galactogogues , Lactation , Meat , Milk, Human , Adolescent , Adult , Animals , Data Collection , Diet , Female , Humans , Perception , Republic of Korea , Safety , Surveys and Questionnaires , Swine , Young Adult
3.
Cell Biol Int ; 32(9): 1099-107, 2008 Sep.
Article in English | MEDLINE | ID: mdl-18550394

ABSTRACT

We have elucidated the cytoprotective effect of annphenone (2,4-dihyroxy-6-methoxy-acetophenone 4-O-beta-D-glucopyranoside) against oxidative stress-induced apoptosis. Annphenone scavenged intracellular reactive oxygen species (ROS) and increased antioxidant enzyme activities. It thereby prevented lipid peroxidation and DNA damage, which was demonstrated by the inhibition of the formation of thiobarbituric acid reactive substance (TBARS), inhibition of the comet tail and decreased phospho-H2A.X expression. Annphenone protected Chinese hamster lung fibroblast (V79-4) cells from cell death via the inhibition of apoptosis induced by hydrogen peroxide (H2O2), as shown by decreased apoptotic nuclear fragmentation, decreased sub-G1 cell population and inhibited mitochondrial membrane potential (Deltapsi) loss. Taken together, these findings suggest that annphenone exhibits antioxidant properties by inhibiting ROS generation and thus protecting cells from H2O2-induced cell damage.


Subject(s)
Acetophenones/pharmacology , Apoptosis/drug effects , Cytoprotection/drug effects , Fibroblasts/cytology , Glucosides/pharmacology , Hydrogen Peroxide/pharmacology , Lung/cytology , Oxidative Stress/drug effects , Acetophenones/chemistry , Animals , Antioxidants/pharmacology , Cell Line , Cricetinae , DNA Damage , Fibroblasts/drug effects , Fibroblasts/enzymology , Free Radical Scavengers/pharmacology , Glucosides/chemistry , Intracellular Space/drug effects , Intracellular Space/metabolism , Lipid Peroxidation/drug effects
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