In the past decade, it has become clear that the immune system can be manipulated to induce cancer regression, durable disease stabilization, and long-term survival in a substantial fraction of cancer patients. Building on this success, members of the Immunology and Cancer (IC) Program aim to better understand the interface between the host immune system and a malignant tumor, and to use this knowledge to develop more effective immunotherapies for the treatment of a broad array of cancer types. The central themes of the Program include: 1) basic immunology relevant to the cancer context (including innate immunity, lymphocyte activation, and peripheral inflammation/tolerance regulation); 2) preclinical mouse models of anti-tumor immunity; and 3) human cancer immunology and immunotherapy. Through the pursuit of these themes, IC members have made fundamental discoveries regarding immune regulation and anti-tumor immunity, and in collaboration with clinical colleagues in the Clinical and Experimental Therapeutics (CET) Program, have leveraged many of these concepts for the development of novel immunotherapies that are now being evaluated in the clinic. The Program is co-led by Thomas Gajewski, MD PhD, Professor of Pathology and Medicine, and Peter Savage, PhD, Associate Professor of Pathology. Dr. Gajewski is a physician-scientist and international leader in the field of tumor immunology and the successful implementation of cancer immunotherapy in human patients. Dr. Savage is a recognized leader in the study of regulatory T cell biology and the role of these cells in the regulation of anti-tumor immunity. There are 18 program members from seven Departments. The IC Program has recruited five new faculty since 2013, including Jason Luke, MD, Melody Swartz, PhD, Jun Huang, PhD, Seungmin Hwang, PhD, and James Labelle, MD, PhD. During the last funding period (2013-2016), program members have published 224 cancer-related articles (with 13% intraprogrammatic and 19% interprogrammatic publications). As of January 2017, Program members hold 36 grants, and are supported by $6.6M (direct costs) in NIH extramural funding, including 6 grants and $1.0M (direct costs) from the NCI. Program members are supported by an additional $2.23 M (direct costs) in non- peer-reviewed support, resulting in total support of $8.9 M (direct costs).

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
5P30CA014599-44
Application #
9701147
Study Section
Subcommittee I - Transistion to Independence (NCI)
Project Start
Project End
Budget Start
2019-04-01
Budget End
2020-03-31
Support Year
44
Fiscal Year
2019
Total Cost
Indirect Cost
Name
University of Chicago
Department
Type
DUNS #
005421136
City
Chicago
State
IL
Country
United States
Zip Code
60637
Hope, C Matthew; Webber, Jemma L; Tokamov, Sherzod A et al. (2018) Tuned polymerization of the transcription factor Yan limits off-DNA sequestration to confer context-specific repression. Elife 7:
Wu, Chengyue; Pineda, Federico; Hormuth 2nd, David A et al. (2018) Quantitative analysis of vascular properties derived from ultrafast DCE-MRI to discriminate malignant and benign breast tumors. Magn Reson Med :
Wong, Gabrielle S; Zhou, Jin; Liu, Jie Bin et al. (2018) Targeting wild-type KRAS-amplified gastroesophageal cancer through combined MEK and SHP2 inhibition. Nat Med 24:968-977
Ni, Kaiyuan; Lan, Guangxu; Chan, Christina et al. (2018) Nanoscale metal-organic frameworks enhance radiotherapy to potentiate checkpoint blockade immunotherapy. Nat Commun 9:2351
Meisel, Marlies; Hinterleitner, Reinhard; Pacis, Alain et al. (2018) Microbial signals drive pre-leukaemic myeloproliferation in a Tet2-deficient host. Nature 557:580-584
Webber, Jemma L; Zhang, Jie; Massey, Alex et al. (2018) Collaborative repressive action of the antagonistic ETS transcription factors Pointed and Yan fine-tunes gene expression to confer robustness in Drosophila. Development 145:
Wei, Jiangbo; Liu, Fange; Lu, Zhike et al. (2018) Differential m6A, m6Am, and m1A Demethylation Mediated by FTO in the Cell Nucleus and Cytoplasm. Mol Cell 71:973-985.e5
Boisclair Lachance, Jean-François; Webber, Jemma L; Hong, Lu et al. (2018) Cooperative recruitment of Yan via a high-affinity ETS supersite organizes repression to confer specificity and robustness to cardiac cell fate specification. Genes Dev 32:389-401
Szmulewitz, Russell Z; Peer, Cody J; Ibraheem, Abiola et al. (2018) Prospective International Randomized Phase II Study of Low-Dose Abiraterone With Food Versus Standard Dose Abiraterone In Castration-Resistant Prostate Cancer. J Clin Oncol 36:1389-1395
Kudron, Michelle M; Victorsen, Alec; Gevirtzman, Louis et al. (2018) The ModERN Resource: Genome-Wide Binding Profiles for Hundreds of Drosophila and Caenorhabditis elegans Transcription Factors. Genetics 208:937-949

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