The Cell Signaling and Gene Regulation Program (Program 1) brings together a group of basic andtranslational investigators dedicated to the study of cancer through research in cell signaling, molecularbiology, systems biology, developmental biology, and chemistry/drug discovery. The program has 46members from 13 Departments, and members have a total of $16,459,487 in peer-reviewed funding with$5,012,818 from the NCI. Program members have been highly-productive, with 599 peer-reviewedpublications, including 7% that were intraprogrammatic, and 15% interprogrammatic publications.The scientific goals of the Cell Signaling and Gene Regulation Program are to determine the basic cellsignaling and gene expression mechanisms that underlie malignancy. To this end, our membership'sresearch focuses on determining the mechanisms whereby genes, and the proteins they encode, functionin both normal and cancerous conditions. In the previous funding period, Program 1 has increased itsmembership size from 25 to 46 members, reflecting a major recruitment of physician-scientists studyingbasic mechanisms of disease, as well as systems biologists. In addition, the UCCRC's outreach tophysical scientists interested in collaborative interdisciplinary cancer research has also enriched themembership of Program 1.Overall, the research objectives of our scientists can be divided into the following five themes: (1) toelucidate the molecular mechanisms of tissue-specific and cell type-specific gene expression; (2) toelucidate the cellular mechanisms underlying cell growth/division and cell survival/death; (3) to understandthe multi-faceted mechanisms leading to cancer metastases; (4) to use large-scale, high-throughputsystems biology approaches and genetic evolutionary approaches to understand cancer biology; and (5) todiscover novel developmental pathways relevant to cancer cell signaling. Although our members' interestsare varied, many common themes have emerged. Moreover, in the current funding period, ourmembership has developed numerous collaborations with clinician scientists both within Program 1 andinterprogramatically, reflecting the increasingly cross-disciplinary and translational nature of our researchprogram. Through pilot funding, quarterly membership meetings, a seminar series, an annual retreat, anda strong basic science training program in cancer biology, Program 1 is poised to continue its successfulin-depth and basic research focus on cancer biology, while nurturing collaborative science that willenhance clinical care of patients at risk or with cancer.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
2P30CA014599-33
Application #
7714228
Study Section
Special Emphasis Panel (ZCA1-RTRB-N (J1))
Project Start
2008-07-22
Project End
2013-03-31
Budget Start
2008-07-22
Budget End
2009-03-31
Support Year
33
Fiscal Year
2008
Total Cost
$24,095
Indirect Cost
Name
University of Chicago
Department
Type
DUNS #
005421136
City
Chicago
State
IL
Country
United States
Zip Code
60637
Liu, Hongtao; Zha, Yuanyuan; Choudhury, Noura et al. (2018) WT1 peptide vaccine in Montanide in contrast to poly ICLC, is able to induce WT1-specific immune response with TCR clonal enrichment in myeloid leukemia. Exp Hematol Oncol 7:1
Nageeb, Shaheen; Vu, Milkie; Malik, Sana et al. (2018) Adapting a religious health fatalism measure for use in Muslim populations. PLoS One 13:e0206898
Ferreira, Caroline M; Williams, Jesse W; Tong, Jiankun et al. (2018) Allergen Exposure in Lymphopenic Fas-Deficient Mice Results in Persistent Eosinophilia Due to Defects in Resolution of Inflammation. Front Immunol 9:2395
Luke, Jason J; Lemons, Jeffrey M; Karrison, Theodore G et al. (2018) Safety and Clinical Activity of Pembrolizumab and Multisite Stereotactic Body Radiotherapy in Patients With Advanced Solid Tumors. J Clin Oncol 36:1611-1618
Wang, Amy Y; Weiner, Howard; Green, Margaret et al. (2018) A phase I study of selinexor in combination with high-dose cytarabine and mitoxantrone for remission induction in patients with acute myeloid leukemia. J Hematol Oncol 11:4
Sample, Ashley; He, Yu-Ying (2018) Mechanisms and prevention of UV-induced melanoma. Photodermatol Photoimmunol Photomed 34:13-24
Jeong, Choongwon; Witonsky, David B; Basnyat, Buddha et al. (2018) Detecting past and ongoing natural selection among ethnically Tibetan women at high altitude in Nepal. PLoS Genet 14:e1007650
Wang, Xin; Wu, Xingye; Zhang, Zhonglin et al. (2018) Monensin inhibits cell proliferation and tumor growth of chemo-resistant pancreatic cancer cells by targeting the EGFR signaling pathway. Sci Rep 8:17914
Brown, Hailey M; Biering, Scott B; Zhu, Allen et al. (2018) Demarcation of Viral Shelters Results in Destruction by Membranolytic GTPases: Antiviral Function of Autophagy Proteins and Interferon-Inducible GTPases. Bioessays 40:e1700231
Karrison, Theodore; Kocherginsky, Masha (2018) Restricted mean survival time: Does covariate adjustment improve precision in randomized clinical trials? Clin Trials 15:178-188

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