TY - JOUR
T1 - Mechanistic examination of walnuts in prevention of breast cancer
AU - Heuvel, John P.Vanden
AU - Belda, Benjamin J.
AU - Hannon, Dan B.
AU - Kris-Etherton, Penny M.
AU - Grieger, Jessica A.
AU - Zhang, Jun
AU - Thompson, Jerry T.
N1 - Funding Information:
This work was funded by grants from the American Institute for Cancer Research and the California Walnut Commission. Neither group had input on interpretation or reporting of the findings.
PY - 2012/10/1
Y1 - 2012/10/1
N2 - Walnuts contain bioactive molecules that may contribute to their beneficial effects, including alpha-linolenic acid (ALA) and phytosterols. In these studies, extracts of walnut, purified compounds, or postprandial serum were examined for effects on breast cancer cell proliferation and gene expression. Extracts derived from walnut oil decreased proliferation of MCF-7 cells, as did ALA and -sitosterol. The gene expression response of ALA in the mouse breast cancer cell line TM2H indicates this molecule has multiple cellular targets with peroxisome proliferator-activated receptor (PPAR) target genes, liver X receptor (LXR), and farnesoid X receptor (FXR) target genes being affected. In transactivation assays, walnut oil extracts increased activity of FXR to a greater extent than the other tested nuclear receptors. When examined separately, walnut components ALA and -sitosterol were the most efficacious activators of FXR. When serum from individuals fed walnut components were applied to MCF-7 cells, there was a correlation between body mass index and breast cancer cell proliferation in vitro. Taken together, these data support an effect of walnut and its bioactive constituents on mammary epithelial cells and that multiple molecular targets may be involved.
AB - Walnuts contain bioactive molecules that may contribute to their beneficial effects, including alpha-linolenic acid (ALA) and phytosterols. In these studies, extracts of walnut, purified compounds, or postprandial serum were examined for effects on breast cancer cell proliferation and gene expression. Extracts derived from walnut oil decreased proliferation of MCF-7 cells, as did ALA and -sitosterol. The gene expression response of ALA in the mouse breast cancer cell line TM2H indicates this molecule has multiple cellular targets with peroxisome proliferator-activated receptor (PPAR) target genes, liver X receptor (LXR), and farnesoid X receptor (FXR) target genes being affected. In transactivation assays, walnut oil extracts increased activity of FXR to a greater extent than the other tested nuclear receptors. When examined separately, walnut components ALA and -sitosterol were the most efficacious activators of FXR. When serum from individuals fed walnut components were applied to MCF-7 cells, there was a correlation between body mass index and breast cancer cell proliferation in vitro. Taken together, these data support an effect of walnut and its bioactive constituents on mammary epithelial cells and that multiple molecular targets may be involved.
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U2 - 10.1080/01635581.2012.717679
DO - 10.1080/01635581.2012.717679
M3 - Article
C2 - 23061909
AN - SCOPUS:84867781731
SN - 0163-5581
VL - 64
SP - 1078
EP - 1086
JO - Nutrition and cancer
JF - Nutrition and cancer
IS - 7
ER -