The overall research objective of this Program Project is to evaluate the potential beneficial or detrimental effects of dietary phytoestrogens on breast cancer progression, adipose tissue and the brain, using well-established laboratory animal models. Although phytoestrogens are consumed by older Americans for their perceived beneficial effects, these estrogenic compounds have not been adequately evaluated for safety, despite increasing consumption of these chemicals at high levels, especially among older women. The theme of this Program Project is that dosage, timing, and duration of exposure will all be determinants of the biological outcome of phytoestrogen exposure in different target tissues. Since both potential risks and benefits need to be evaluated, these studies cannot be conducted in humans for ethical reasons and can best be conducted in appropriate pre-clinical laboratory animal models. The proposed studies provide a systematic evaluation of the role that various regimens of phytoestrogen exposure may have on target organs that are of special relevance in aging, and these studies will also seek to determine the mechanism of phytoestrogen effects on these different target tissues. In summary, the overall goal of the P01 is to conduct highly interactive investigations of the effects of phytoestrogen dietary exposure using well established animal models, each having specific advantages for the study of: breast cancer progression to hormone independence, obesity and risk of diabetes, and cognitive function. This goal will be achieved through four complementary, synergistic projects: (1) Genistein and Endocrine Resistance in Breast Tumors, (2) Dietary Phytoestrogens and Adipocyte Development, (3) Dietary Estrogens and Cognitive Function During Aging, and (4) Phytoestrogen Action Through Estrogen Receptors alpha and beta. Investigators will be aided by an Administrative Core that oversees inter-project meetings and provides budgetary, reporting and external advisory needs, an Analytical and Bioavailability Core that will provide analysis and standardization of blood and tissue isoflavone levels for projects 1-3, and a Dietary, Genomics and Chemistry Synthesis Core that will provide uniform diets, gene expression profiling analysis by microarray and quantitative PCR methods, and chemical synthesis of phytoestrogens and phytoestrogen metabolites.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Research Program Projects (P01)
Project #
5P01AG024387-03
Application #
7117785
Study Section
Special Emphasis Panel (ZAG1-ZIJ-6 (M2))
Program Officer
Fuldner, Rebecca A
Project Start
2004-09-30
Project End
2009-08-31
Budget Start
2006-09-01
Budget End
2007-08-31
Support Year
3
Fiscal Year
2006
Total Cost
$1,526,683
Indirect Cost
Name
University of Illinois Urbana-Champaign
Department
Nutrition
Type
Schools of Earth Sciences/Natur
DUNS #
041544081
City
Champaign
State
IL
Country
United States
Zip Code
61820
Pisani, Samantha L; Neese, Steven L; Katzenellenbogen, John A et al. (2016) Estrogen Receptor-Selective Agonists Modulate Learning in Female Rats in a Dose- and Task-Specific Manner. Endocrinology 157:292-303
Ferguson, Lynnette R; Chen, Helen; Collins, Andrew R et al. (2015) Genomic instability in human cancer: Molecular insights and opportunities for therapeutic attack and prevention through diet and nutrition. Semin Cancer Biol 35 Suppl:S5-S24
Andrade, Juan E; Ju, Young H; Baker, Chandra et al. (2015) Long-term exposure to dietary sources of genistein induces estrogen-independence in the human breast cancer (MCF-7) xenograft model. Mol Nutr Food Res 59:413-23
Korol, Donna L; Pisani, Samantha L (2015) Estrogens and cognition: Friends or foes?: An evaluation of the opposing effects of estrogens on learning and memory. Horm Behav 74:105-15
Yang, Xujuan; Belosay, Aashvini; Du, Mengyuan et al. (2013) Estradiol increases ER-negative breast cancer metastasis in an experimental model. Clin Exp Metastasis 30:711-21
Neese, Steven L; Bandara, Suren B; Schantz, Susan L (2013) Working memory in bisphenol-A treated middle-aged ovariectomized rats. Neurotoxicol Teratol 35:46-53
Neese, Steven L; Korol, Donna L; Schantz, Susan L (2013) Voluntary exercise impairs initial delayed spatial alternation performance in estradiol treated ovariectomized middle-aged rats. Horm Behav 64:579-88
Neese, Steven L; Bandara, Suren B; Doerge, Daniel R et al. (2012) Effects of multiple daily genistein treatments on delayed alternation and a differential reinforcement of low rates of responding task in middle-aged rats. Neurotoxicol Teratol 34:187-95
Pisani, Samantha L; Neese, Steven L; Doerge, Daniel R et al. (2012) Acute genistein treatment mimics the effects of estradiol by enhancing place learning and impairing response learning in young adult female rats. Horm Behav 62:491-9
Bergamaschi, A; Katzenellenbogen, B S (2012) Tamoxifen downregulation of miR-451 increases 14-3-3? and promotes breast cancer cell survival and endocrine resistance. Oncogene 31:39-47

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