A campus-wide Prostate Cancer Research Program has been developed with collaboration of multiple schools and institutes at UCLA. The Prostate Cancer Program area has recently been named a full Program Area of the Jonsson Comprehensive Cancer Center (JCCC). This germinal program provides the basis for this SPORE application. The purpose of the SPORE is, along with other SPORE institutions, to contribute to the progress in the diagnosis, prevention, and treatment of prostate cancer. The SPORE project has two major objectives: 1. To develop multiple translational basic research and community-based research projects with an emphasis on minority populations. Four laboratory research projects will apply institutional research on gene expression and signaling, to prognosis and treatment of prostate cancer. One project will build on the experience of institutional investigators to address innovative aspects of dietary control of prostate cancer. 2. To develop new prostate cancer research and career development to advance translational research. This will be effected through existing and continued institutional support as well as career development programs and developmental research programs. The emphasis in all research projects is rapid translation to clinical trials. Existing clinical research programs have been coordinated to provide the best possible access to study patients with all stages of prostate cancer. The four basic research projects are linked, in that they a) are clearly translatable, b) are based on basic work within the individual investigator's own laboratories, and c) provide new strategies for targeting specific signaling pathways important in prostate cancer. Information from these studies also provides prognostic information and will add to the current clinical and molecular markers of prognosis for localized prostate cancer. An external Advisory Board will participate in the supervision and analysis of SPORE progress in all research and administrative areas. In collaboration with the JCCC, the SPORE represents a major interdisciplinary, collaborative, and translational program which promises to make a significant impact on prostate cancer mortality and morbidity.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Specialized Center (P50)
Project #
5P50CA092131-04
Application #
6934673
Study Section
Special Emphasis Panel (ZCA1-GRB-V (J1))
Program Officer
Hruszkewycz, Andrew M
Project Start
2002-09-15
Project End
2007-06-30
Budget Start
2005-07-01
Budget End
2006-06-30
Support Year
4
Fiscal Year
2005
Total Cost
$2,314,075
Indirect Cost
Name
University of California Los Angeles
Department
Urology
Type
Schools of Medicine
DUNS #
092530369
City
Los Angeles
State
CA
Country
United States
Zip Code
90095
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
Li, Jiayun; Speier, William; Ho, King Chung et al. (2018) An EM-based semi-supervised deep learning approach for semantic segmentation of histopathological images from radical prostatectomies. Comput Med Imaging Graph 69:125-133
Kang, Jung J; Reiter, Robert E; Kummer, Nicolas et al. (2018) Wrong to be Right: Margin Laterality is an Independent Predictor of Biochemical Failure After Radical Prostatectomy. Am J Clin Oncol 41:1-5

Showing the most recent 10 out of 339 publications