Breast cancer is one of the most common cancers in women. Anti-estrogens are now used in the treatment of estrogen-dependent breast cancers. Another related treatment includes the use of aromatase inhibitors, which block the conversion of androgen to estrogen. Recently, the orphan nuclear receptor, liver related homologue 1 (LRH1) has been shown to control gene expression of aromatase in breast cancer tissue. Thus, knowing how LRH1 activity is regulated may provide insights into how aromatase activity is modulated and may, provide new strategies for lowering estrogen levels in breast cancer. My proposed study involves identifying protein partners of LRH1 and how post-translational modifications affect LRH1 activity. For my first aim, I will use a yeast genetic strategy to screen for LRH1 cofactors when LRH1 is bound to its native DNA response element. I will screen cDNAs libraries made from breast cancer cell lines to identify cancer-specific interacting partners ofLRH1. In my second aim, I will determine the role of SUMOylation on LRH1 function since our lab has found that LRH1 interacts with the SUMO-conjugating enzyme UBC9, and the closest homologue of LRH1, steroidogenic factor 1 (SF-1) is SUMOyIated. Ultimately, I want to know if there are selective LRH1 protein partners in breast cancer tissue and how SUMOylation might modulate protein-protein interactions and function of LRH1.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
5F32CA103271-02
Application #
6787657
Study Section
Special Emphasis Panel (ZRG1-F06 (20))
Program Officer
Lohrey, Nancy
Project Start
2003-08-01
Project End
2006-07-31
Budget Start
2004-08-01
Budget End
2005-07-31
Support Year
2
Fiscal Year
2004
Total Cost
$42,976
Indirect Cost
Name
University of California San Francisco
Department
Physiology
Type
Schools of Medicine
DUNS #
094878337
City
San Francisco
State
CA
Country
United States
Zip Code
94143