PROJECT 002 ? HOST-TUMOR RESEARCH PROGRAM PROJECT SUMMARY/ABSTRACT The Host-Tumor Interactions Research Program (HT) consists of basic, translational and clinical scientists focused on discovering the interactions between tumor cells and their host, and developing strategies to interrupt those interactions in order to target and control tumor progression and metastasis. The central theme of HT is that tumor growth, invasion and metastasis depend not only on the tumor cell alone, but also on the complex interactions between the tumor cells and the host. In light of these realizations, the long-term scientific goal of HT is to develop a detailed and mechanistic understanding of not just the tumor cell and tumor mutations, but also all the components of the host microenvironment that influence cancer and the response to cancer therapy. These interactions are best studied by integrating knowledge and paradigms from many disciplines, including those not typically associated with cancer biology and oncology. In particular, in this renewal HT has taken advantage of the strength of its membership to explicitly incorporate individuals with imaging and modeling expertise to rigorously investigate the scientific goals of HT, which are to: ? Identify and validate molecular targets involved in communication between the tumor and host that contribute to tumor progression using sequencing and antibodies, probes and small molecules, imaging and computational modeling ? Develop in vitro and in vivo systems to test therapeutics and determine their mechanism of action ? Develop new methodologies capable of discovering and validating novel therapeutic targets ? Establish dynamic, multi-disciplinary collaborations that will accelerate these discoveries With these larger goals in mind, the strong expertise of the program is focused on cell-cell and cell-matrix interactions, angiogenesis and vasculogenesis, inflammation and tumor imaging and modeling. There are 39 program members from 15 departments and four schools with $7.6M in NCI funding and $6.4M in other peer-reviewed cancer-related funding. Out of 579 publications, 16% are intra-programmatic and 38% are inter-programmatic. Members also have 150 collaborative publications with investigators at other institutions.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
6P30CA068485-20
Application #
9248563
Study Section
Subcommittee I - Transistion to Independence (NCI)
Project Start
Project End
Budget Start
2016-04-30
Budget End
2016-08-31
Support Year
20
Fiscal Year
2015
Total Cost
Indirect Cost
Name
Vanderbilt University Medical Center
Department
Type
DUNS #
079917897
City
Nashville
State
TN
Country
United States
Zip Code
37232
Schulte, Michael L; Fu, Allie; Zhao, Ping et al. (2018) Pharmacological blockade of ASCT2-dependent glutamine transport leads to antitumor efficacy in preclinical models. Nat Med 24:194-202
Petersen, Christine P; Meyer, Anne R; De Salvo, Carlo et al. (2018) A signalling cascade of IL-33 to IL-13 regulates metaplasia in the mouse stomach. Gut 67:805-817
Maacha, Selma; Hong, Jun; von Lersner, Ariana et al. (2018) AXL Mediates Esophageal Adenocarcinoma Cell Invasion through Regulation of Extracellular Acidification and Lysosome Trafficking. Neoplasia 20:1008-1022
Galligan, James J; Wepy, James A; Streeter, Matthew D et al. (2018) Methylglyoxal-derived posttranslational arginine modifications are abundant histone marks. Proc Natl Acad Sci U S A 115:9228-9233
Davenport, James R; Su, Timothy; Zhao, Zhiguo et al. (2018) Modifiable lifestyle factors associated with risk of sessile serrated polyps, conventional adenomas and hyperplastic polyps. Gut 67:456-465
Wang, Jing; Zhao, Yue; Zhou, Xiaofan et al. (2018) Nascent RNA sequencing analysis provides insights into enhancer-mediated gene regulation. BMC Genomics 19:633
Zhao, Shilin; Li, Chung-I; Guo, Yan et al. (2018) RnaSeqSampleSize: real data based sample size estimation for RNA sequencing. BMC Bioinformatics 19:191
Croessmann, Sarah; Sheehan, Jonathan H; Lee, Kyung-Min et al. (2018) PIK3CA C2 Domain Deletions Hyperactivate Phosphoinositide 3-kinase (PI3K), Generate Oncogene Dependence, and Are Exquisitely Sensitive to PI3K? Inhibitors. Clin Cancer Res 24:1426-1435
Pannala, Venkat R; Wall, Martha L; Estes, Shanea K et al. (2018) Metabolic network-based predictions of toxicant-induced metabolite changes in the laboratory rat. Sci Rep 8:11678
Salisbury-Ruf, Christi T; Bertram, Clinton C; Vergeade, Aurelia et al. (2018) Bid maintains mitochondrial cristae structure and function and protects against cardiac disease in an integrative genomics study. Elife 7:

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