The long term goal of this project is to develop strategies to improve treatment and prevent breast cancer. The aromatase inhibitors that we pioneered in earlier phases of this grant are now proving to be effective in the clinic. During the current period, we have made a number of significant observations indicating that breast tumor aromatase expression has an important role in tumor promotion. These findings form the basis for the proposed studies. We have detected significant aromatase expression in tumors of about 60 percent of patients. We now propose to investigate in Specific Aim 1, whether intratumoral aromatase expression, measured by our ICC method in paraffin sections, is correlated with the response of breast cancer patients to aromatase inhibitor treatment. This information may predict the value of inhibitor treatment for individual patients. We have successfully isolated cells from normal human breast tissue and from metastatic breast cancer.
In Specific Aim 2, we will determine the mechanisms of aromatase gene regulation in luminal epithelial cells and fibroblasts from normal human breast tissue and in metastatic breast cancer cells. We will identify the promoter regions of the aromatase gene controlling expression of the enzyme.
In Specific Aim 3, we will determine whether aromatase inhibitors are more effective in combination with specific estrogen receptor modulator raloxifene than either alone in our intratumoral aromatase model. In addition, we will investigate mechanisms of letrozole antitumor action and development of resistance and the effect of antiestrogens and other aromatase inhibitors on letrozole resistant growth this model. These studies could provide important new leads into the mechanisms of aromatase inhibitor antitumor actions and development of resistance and may ultimately be useful for identifying patients who are likely to be responsive/resistant to treatment.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
5R01CA062483-20
Application #
6512953
Study Section
Biochemical Endocrinology Study Section (BCE)
Program Officer
Sathyamoorthy, Neeraja
Project Start
1980-09-01
Project End
2003-03-31
Budget Start
2002-04-01
Budget End
2003-03-31
Support Year
20
Fiscal Year
2002
Total Cost
$255,615
Indirect Cost
Name
University of Maryland Baltimore
Department
Pharmacology
Type
Schools of Medicine
DUNS #
003255213
City
Baltimore
State
MD
Country
United States
Zip Code
21201
Schech, Amanda J; Shah, Preeti; Yu, Stephen et al. (2015) Histone deacetylase inhibitor entinostat in combination with a retinoid downregulates HER2 and reduces the tumor initiating cell population in aromatase inhibitor-resistant breast cancer. Breast Cancer Res Treat 152:499-508
Khatri, Raju; Shah, Preeti; Guha, Rupa et al. (2015) Aromatase Inhibitor-Mediated Downregulation of INrf2 (Keap1) Leads to Increased Nrf2 and Resistance in Breast Cancer. Mol Cancer Ther 14:1728-37
Schech, Amanda J; Kazi, Armina A; Gilani, Rabia A et al. (2013) Zoledronic acid reverses the epithelial-mesenchymal transition and inhibits self-renewal of breast cancer cells through inactivation of NF-?B. Mol Cancer Ther 12:1356-66
Sabnis, Gauri J; Goloubeva, Olga G; Kazi, Armina A et al. (2013) HDAC inhibitor entinostat restores responsiveness of letrozole-resistant MCF-7Ca xenografts to aromatase inhibitors through modulation of Her-2. Mol Cancer Ther 12:2804-16
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Gilani, Rabia A; Kazi, Armina A; Shah, Preeti et al. (2012) The importance of HER2 signaling in the tumor-initiating cell population in aromatase inhibitor-resistant breast cancer. Breast Cancer Res Treat 135:681-92
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Tobin, Lisa A; Robert, Carine; Nagaria, Pratik et al. (2012) Targeting abnormal DNA repair in therapy-resistant breast cancers. Mol Cancer Res 10:96-107
Schech, Amanda J; Nemieboka, Brandon E; Brodie, Angela H (2012) Zoledronic acid inhibits aromatase activity and phosphorylation: potential mechanism for additive zoledronic acid and letrozole drug interaction. J Steroid Biochem Mol Biol 132:195-202
Tilghman, Syreeta L; Sabnis, Gauri; Brodie, Angela M H (2011) Upregulation of AIB1, aromatase and ER* provides long-term estrogen-deprived human breast cancer cells with a mechanistic growth advantage for survival. Horm Mol Biol Clin Investig 3:357-366

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