The overall goal of the Cancer and Immunity Program is to provide new scientific insights into the relationships between immune system and tumors and to define target molecules and strategies for new immune-based therapies for cancer. Specific scientific goals of the Cancer and Immunity Program are: (1) to explore the relationship between tumors and leukocytes in mouse models of cancer to gain insights into the ability of the immune system to promote or deter tumorigenesis;(2) to use mouse models of cancer for preclinical studies of novel immune-based therapies, such as blocking newly discovered inhibitory regulators of the immune system, and therapeutic vaccines;(3) to identify molecules in the immune system that regulate the ability of the innate and adaptive immune system to mediate anti-tumor activity, without eliciting severe autoimmunity;(4) to define signaling pathways through immune receptors affecting cell survival and apoptosis, which may serve as therapeutic targets for cancer;(5) to study the relationship between viral infections and malignancy, particularly in immunodeficient patients with HIV infection, and to develop new approaches to the prevention and treatment of malignancy in this population;and (6) to conduct clinical trials of new immune-based immunotherapeutics in cancer, with a focus on prostate cancer, and study the immune response in individual undergoing therapy to potentially identify new targets for antigen-specific therapeutic vaccines. The Program consists of 25 faculty from 11 departments in the School of Medicine. The Program has $20,640,449 Total peer reviewed support for the last budget year. The Program has 5% intra-programmatic and 30% inter-programmatic publications.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
5P30CA082103-13
Application #
8292260
Study Section
Subcommittee G - Education (NCI)
Project Start
Project End
Budget Start
2011-06-01
Budget End
2012-05-31
Support Year
13
Fiscal Year
2011
Total Cost
$69,688
Indirect Cost
Name
University of California San Francisco
Department
Type
DUNS #
094878337
City
San Francisco
State
CA
Country
United States
Zip Code
94143
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
Ryu, Jae Kyu; Rafalski, Victoria A; Meyer-Franke, Anke et al. (2018) Fibrin-targeting immunotherapy protects against neuroinflammation and neurodegeneration. Nat Immunol 19:1212-1223
Zhou, Yu; Zou, Hao; Yau, Christina et al. (2018) Discovery of internalizing antibodies to basal breast cancer cells. Protein Eng Des Sel 31:17-28
Tat, David; Kenfield, Stacey A; Cowan, Janet E et al. (2018) Milk and other dairy foods in relation to prostate cancer recurrence: Data from the cancer of the prostate strategic urologic research endeavor (CaPSUREā„¢). Prostate 78:32-39
Guydish, Joseph; Tajima, Barbara; Le, Thao et al. (2018) Do cigarette graphic warnings encourage smokers to attend a smoking cessation programme: a quasi-experimental study. Tob Control 27:43-49
Dvorak, Christopher C; Satwani, Prakash; Stieglitz, Elliot et al. (2018) Disease burden and conditioning regimens in ASCT1221, a randomized phase II trial in children with juvenile myelomonocytic leukemia: A Children's Oncology Group study. Pediatr Blood Cancer 65:e27034
Fan, Qi Wen; Nicolaides, Theodore P; Weiss, William A (2018) Inhibiting 4EBP1 in Glioblastoma. Clin Cancer Res 24:14-21

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