PROJECT 003 ? SIGNAL TRANSDUCTION AND CHEMICAL BIOLOGY PROJECT SUMMARY/ABSTRACT The Signal Transduction and Chemical Biology Research Program (ST) is an active group of basic scientists focused on signaling networks that control cell proliferation, stem cell function and tumorigenesis, and the development of chemical inhibitors for these signaling pathways. The Program has changed the name from Signal Transduction and Cell Proliferation since the last renewal to reflect that inhibitors of mutant or activated signaling components have had a major impact in genotype-driven clinical trials and that future therapeutic advances will require a better understanding of signaling networks and how these networks change and evolve during cancer progression and in response to inhibitors (e.g., mechanisms of resistance). ST goals are to understand how perturbations in signaling networks drive the development of cancer, to use this information to identify therapeutic targets, and to develop new chemical tools or even lead compounds for new therapeutics. This Program seeks to leverage the genetic analysis of cancer (e.g., TCGA data and/or the CE Program), stem cell biology and high-content systems analysis of signaling networks for the identification of key nodes that can be tested in model systems (e.g., using new technology such as CRISPR/Cas9), used for the synthesis of inhibitors, and that eventually can be targeted therapeutically. ST is organized into several groups with common interests: signaling networks, chemical biology, stem cell biology and cell cycle control. The overall goals are to promote outstanding basic research in signaling networks and to provide intellectual support for clinical programs working with inhibitors of signaling and cell cycle pathways; to stimulate interactions among the Program membership to accelerate discovery; to stimulate the use of new technologies; and to work closely with Vanderbilt-Ingram Cancer Center (VICC) shared resources to make new instrumentation and methods available that will accelerate cancer research. There are 41 program members from 13 departments and three schools, with $3.9M in NCI funding and $6.3M in other peer-reviewed cancer-related funding. Out of 458 publications, 12% are intra-programmatic and 28% are inter-programmatic. Members also have 143 collaborative publications with investigators at other institutions.

Public Health Relevance

PROJECT 003 ? SIGNAL TRANSDUCTION AND CHEMICAL BIOLOGY PROJECT NARRATIVE Per the PAR-13-386 FOA, the project narrative is not applicable for the Signal Transduction and Chemical Biology Research Program.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
5P30CA068485-23
Application #
9553530
Study Section
Subcommittee I - Transistion to Independence (NCI)
Project Start
Project End
Budget Start
2018-09-01
Budget End
2019-08-31
Support Year
23
Fiscal Year
2018
Total Cost
Indirect Cost
Name
Vanderbilt University Medical Center
Department
Type
DUNS #
079917897
City
Nashville
State
TN
Country
United States
Zip Code
37232
Takata, Yumie; Xiang, Yong-Bing; Burk, Raymond F et al. (2018) Plasma selenoprotein P concentration and lung cancer risk: results from a case-control study nested within the Shanghai Men's Health Study. Carcinogenesis 39:1352-1358
Feng, Yinnian; Reinherz, Ellis L; Lang, Matthew J (2018) ?? T Cell Receptor Mechanosensing Forces out Serial Engagement. Trends Immunol 39:596-609
Sucre, Jennifer M S; Deutsch, Gail H; Jetter, Christopher S et al. (2018) A Shared Pattern of ?-Catenin Activation in Bronchopulmonary Dysplasia and Idiopathic Pulmonary Fibrosis. Am J Pathol 188:853-862
Rogers, Meredith C; Lamens, Kristina D; Shafagati, Nazly et al. (2018) CD4+ Regulatory T Cells Exert Differential Functions during Early and Late Stages of the Immune Response to Respiratory Viruses. J Immunol 201:1253-1266
Rosenberg, Adam J; Nickels, Michael L; Schulte, Michael L et al. (2018) Automated radiosynthesis of 5-[11C]l-glutamine, an important tracer for glutamine utilization. Nucl Med Biol 67:10-14
Dean, Donnatesa A L; Griffith, Derek M; McKissic, Sydika A et al. (2018) Men on the Move-Nashville: Feasibility and Acceptability of a Technology-Enhanced Physical Activity Pilot Intervention for Overweight and Obese Middle and Older Age African American Men. Am J Mens Health 12:798-811
Choi, Eunyoung; Lantz, Tyler L; Vlacich, Gregory et al. (2018) Lrig1+ gastric isthmal progenitor cells restore normal gastric lineage cells during damage recovery in adult mouse stomach. Gut 67:1595-1605
Parl, Fritz F; Crooke, Philip S; Plummer Jr, W Dale et al. (2018) Genomic-Epidemiologic Evidence That Estrogens Promote Breast Cancer Development. Cancer Epidemiol Biomarkers Prev 27:899-907
Marks, Christian R; Shonesy, Brian C; Wang, Xiaohan et al. (2018) Activated CaMKII? Binds to the mGlu5 Metabotropic Glutamate Receptor and Modulates Calcium Mobilization. Mol Pharmacol 94:1352-1362
Singh, Kshipra; Coburn, Lori A; Asim, Mohammad et al. (2018) Ornithine Decarboxylase in Macrophages Exacerbates Colitis and Promotes Colitis-Associated Colon Carcinogenesis by Impairing M1 Immune Responses. Cancer Res 78:4303-4315

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