Cumulative exposure to excessive levels of estrogen is a major risk factor for breast cancer. Estrogen and its cellular receptor, estrogen receptor (ER), are involved in regulating normal breast epithelial and tumor cell proliferation, and ER is both a prognostic marker and a therapeutic target in breast cancer treatment. Selective estrogen receptor modulators (SERMs) have been shown to be effective in both preventing and treating ER- positive breast cancers. ER is also a molecular target of phytoestrogens, a group of plant-derived phenolic compounds which are structurally similar to estrogen and SERMs. This raises possibility that intake of foods containing these compounds may help prevent breast cancers. A better understanding of ER functions and the impact of SERMs and phytoestrogens on their molecular mechanisms, therefore, should lead to both better understanding and application of these compounds in cancer prevention. Recently published microarray studies and whole-genome ER binding site mapping experiments suggest that ER can alternatively directly repress the expression of a significant subset of target genes. Little is known regarding the mechanisms of transcriptional repression by ER, although the data indicate that many genes are directly down-regulated following estrogen treatment and the effects of SERMs and phytoestrogens on repressed target gene expression and mechanisms of transcriptional repression by ER are also unclear.
The aims of our proposed studies are to identify transcription factors which may facilitate ER-mediated transcriptional repression and to determine the effects of SERMs and phytoestrogens on these and other potential mechanisms of transcriptional repression by ER.
These aims and corresponding experiments outlined in this application seek to shed light on a novel aspect of transcriptional regulation by ER, a molecular target of SERMs and phytoestrogens, and the effects of these compounds on newly discovered target mechanisms. Findings from the proposed studies will not only establish a new molecular paradigm for understanding and describing ER and SERM and phytoestrogen functions but will also facilitate future studies on the potential role of SERMs and phytoestrogens and target mechanisms in cancer prevention.

Public Health Relevance

Estrogen receptor in breast epithelial cells is a target for drugs which can lower the risk of breast cancer. Drugs called selective estrogen receptor modulators (SERMs) which target estrogen receptor have been shown to be effective in preventing breast cancer. There is also some evidence which suggests that phytoestrogens, compounds found in certain vegetables, fruits, and legumes, can also bind estrogen receptor and possibly help prevent breast cancer. We have recently discovered new functions for estrogen receptor, and we are proposing to carry out studies to better understand these new functions and how they might be affected by SERMs and phytoestrogens. Results from these studies should provide insights into the functions of SERMs and dietary phytoestrogens and may suggest novel strategies for breast cancer prevention.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Small Research Grants (R03)
Project #
1R03CA143981-01
Application #
7792169
Study Section
Special Emphasis Panel (ZCA1-SRLB-F (O1))
Program Officer
Emenaker, Nancy J
Project Start
2009-09-28
Project End
2010-08-31
Budget Start
2009-09-28
Budget End
2010-08-31
Support Year
1
Fiscal Year
2009
Total Cost
$75,000
Indirect Cost
Name
Brigham Young University
Department
Microbiology/Immun/Virology
Type
Schools of Arts and Sciences
DUNS #
009094012
City
Provo
State
UT
Country
United States
Zip Code
84602