The goal of this proposal is to examine the role of prostate stem cell antigen (PSCA) in the prognosis and therapy of prostate cancer. PSCA is a cell surface antigen, which is overexpressed in approximately 40 percent of primary prostate cancers and in as many as 100 percent of metastatic ones. PSCA is also overexpressed in a majority of transitional cell and pancreatic carcinomas. Overexpression of PSCA in prostate cancer correlates with adverse clinicopathologic features, including advanced tumor stage, grade and MYC amplification. A monoclonal antibody directed against PSCA inhibits tumorigenesis, slows tumor growth, prolongs survival and prevents metastasis in a preclinical xenograft model. These data suggest that PSCA may have utility as a prognostic marker and/or therapeutic target in prostate cancer. The overall goals of this project are to determine the prognostic utility of PSCA in patients with clinically localized prostate cancer and to understand and enhance the therapeutic utility of monoclonal antibodies directed against this target. Finally, we intend to translate the knowledge gained from preclinical evaluation of PSCA as a prognostic and therapeutic target into a pilot human clinical trial in which we ask whether PSCA monoclonal antibodies are safe and can localize to PSCA-overexpressing tumors in high-risk individuals undergoing radical prostatectorny. These studies are expected to lead to larger clinical trials examining the therapeutic efficacy of PSCA antibodies.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Specialized Center (P50)
Project #
1P50CA092131-01A1
Application #
6689881
Study Section
Special Emphasis Panel (ZCA1)
Project Start
2002-09-15
Project End
2007-06-30
Budget Start
Budget End
Support Year
1
Fiscal Year
2002
Total Cost
Indirect Cost
Name
University of California Los Angeles
Department
Type
DUNS #
119132785
City
Los Angeles
State
CA
Country
United States
Zip Code
90095
Vidal, Adriana C; Howard, Lauren E; de Hoedt, Amanda et al. (2018) Neutrophil, lymphocyte and platelet counts, and risk of prostate cancer outcomes in white and black men: results from the SEARCH database. Cancer Causes Control 29:581-588
Vidal, Adriana C; Howard, Lauren E; de Hoedt, Amanda et al. (2018) Obese patients with castration-resistant prostate cancer may be at a lower risk of all-cause mortality: results from the Shared Equal Access Regional Cancer Hospital (SEARCH) database. BJU Int 122:76-82
Jelinek, David; Flores, Aimee; Uebelhoer, Melanie et al. (2018) Mapping Metabolism: Monitoring Lactate Dehydrogenase Activity Directly in Tissue. J Vis Exp :
Lee, John K; Bangayan, Nathanael J; Chai, Timothy et al. (2018) Systemic surfaceome profiling identifies target antigens for immune-based therapy in subtypes of advanced prostate cancer. Proc Natl Acad Sci U S A 115:E4473-E4482
Mitra, Mithun; Lee, Ha Neul; Coller, Hilary A (2018) Determining Genome-wide Transcript Decay Rates in Proliferating and Quiescent Human Fibroblasts. J Vis Exp :
Zou, Yongkang; Qi, Zhi; Guo, Weilong et al. (2018) Cotargeting the Cell-Intrinsic and Microenvironment Pathways of Prostate Cancer by PI3K?/?/? Inhibitor BAY1082439. Mol Cancer Ther 17:2091-2099
Henning, Susanne M; Galet, Colette; Gollapudi, Kiran et al. (2018) Phase II prospective randomized trial of weight loss prior to radical prostatectomy. Prostate Cancer Prostatic Dis 21:212-220
Miller, Eric T; Salmasi, Amirali; Reiter, Robert E (2018) Anatomic and Molecular Imaging in Prostate Cancer. Cold Spring Harb Perspect Med 8:
Navarro, Héctor I; Goldstein, Andrew S (2018) HoxB13 mediates AR-V7 activity in prostate cancer. Proc Natl Acad Sci U S A 115:6528-6529
Mitra, Mithun; Ho, Linda D; Coller, Hilary A (2018) An In Vitro Model of Cellular Quiescence in Primary Human Dermal Fibroblasts. Methods Mol Biol 1686:27-47

Showing the most recent 10 out of 339 publications