) The Genitourinary (GU) Cancer Program is an interdisciplinary group that includes members from 10 academic departments: Anatomy, Biochemistry & Biophysics, Cellular & Molecular Pharmacology, Laboratory Medicine, Medicine, Microbiology & Immunology, Pathology, Radiation Oncology, Radiology, and Urology working together on cancer of the bladder, kidney, and prostate. The common interest that spurred formation of this Program and fuels its existence is the utilization of basic research in genetic, molecular, and cellular biology to understand the origins and mechanisms of progression of genitourinary cancers, and to use this knowledge to develop novel approaches to their diagnosis and treatment. Current and developing research is focused on the molecular pathology of prostate cancer-induced angiogenesis, stromal-epithelial interactions in prostate cancer, and the genetic basis for hormone refractory prostate cancer (HRPC). Major foci in clinical research are the use of immunotherapy and anti-angiogenic treatments in HRPC, and developing novel MRI/MRSI technology for evaluating prostate cancer. Monthly Program conferences are highly interactive and very well attended by faculty, post-docs, and graduate students. From these meetings, collaborations have developed and grown at several levels. Several NIH RO1 grants and a Protease in Cancer PPG, as well as major grants from CaP Cure for clinical research, provide considerable resources for the Program.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
5P30CA082103-02
Application #
6348996
Study Section
Subcommittee E - Prevention &Control (NCI)
Project Start
2000-08-01
Project End
2001-07-31
Budget Start
Budget End
Support Year
2
Fiscal Year
2000
Total Cost
Indirect Cost
Name
University of California San Francisco
Department
Type
DUNS #
073133571
City
San Francisco
State
CA
Country
United States
Zip Code
94143
An, Zhenyi; Aksoy, Ozlem; Zheng, Tina et al. (2018) Epidermal growth factor receptor and EGFRvIII in glioblastoma: signaling pathways and targeted therapies. Oncogene 37:1561-1575
Behr, Spencer C; Villanueva-Meyer, Javier E; Li, Yan et al. (2018) Targeting iron metabolism in high-grade glioma with 68Ga-citrate PET/MR. JCI Insight 3:
Rubenstein, James L; Geng, Huimin; Fraser, Eleanor J et al. (2018) Phase 1 investigation of lenalidomide/rituximab plus outcomes of lenalidomide maintenance in relapsed CNS lymphoma. Blood Adv 2:1595-1607
An, Zhenyi; Knobbe-Thomsen, Christiane B; Wan, Xiaohua et al. (2018) EGFR Cooperates with EGFRvIII to Recruit Macrophages in Glioblastoma. Cancer Res 78:6785-6794
Olshen, Adam; Wolf, Denise; Jones, Ella F et al. (2018) Features of MRI stromal enhancement with neoadjuvant chemotherapy: a subgroup analysis of the ACRIN 6657/I-SPY TRIAL. J Med Imaging (Bellingham) 5:011014
Li, Megan; Kroetz, Deanna L (2018) Bevacizumab-induced hypertension: Clinical presentation and molecular understanding. Pharmacol Ther 182:152-160
Brunner, Katja; John, Constance M; Phillips, Nancy J et al. (2018) Novel Campylobacter concisus lipooligosaccharide is a determinant of inflammatory potential and virulence. J Lipid Res 59:1893-1905
Felix, Janine F; Joubert, Bonnie R; Baccarelli, Andrea A et al. (2018) Cohort Profile: Pregnancy And Childhood Epigenetics (PACE) Consortium. Int J Epidemiol 47:22-23u
Cobler, Lara; Zhang, Hui; Suri, Poojan et al. (2018) xCT inhibition sensitizes tumors to ?-radiation via glutathione reduction. Oncotarget 9:32280-32297
Li, Megan; Mulkey, Flora; Jiang, Chen et al. (2018) Identification of a Genomic Region between SLC29A1 and HSP90AB1 Associated with Risk of Bevacizumab-Induced Hypertension: CALGB 80405 (Alliance). Clin Cancer Res 24:4734-4744

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