Program 7: Developmental Therapeutics has, as its principal goal, the development and implementation of human cancer clinical research based on discovery science. The Program emphasizes two subprograms, 1) Immune Therapy and 2) Targeted Therapy, Biomarkers and Imaging. The two subprograms are led respectively by Craig L. Slingluff, M.D., Department of Surgery, and by Geoffrey R. Weiss, M.D., Department of Internal Medicine. The Program has 49 members from 19 different departments or divisions of the University of Virginia Health System. Investigators of this Program are supported by $3.6 million from the NCI and by a total of $9.2 million from all sources. The goals of Program 7 include the development of investigator-initiated clinical trials based in the discovery science of laboratories within the Cancer Center, expansion of the Clinical Trials Office as a comprehensive resource for support of the clinical investigator, and recruitment of new clinical scientists to the program. The Immune Therapy Subprogram is invested in a broad array of clinical trials evaluating multipeptide vaccines in malignant melanoma, colorectal cancer and ovarian cancer, antibody therapies of hematological malignancies, and cytokine therapies of melanoma and renal cell carcinoma. Investigators of the Targeted Therapy, Biomarkers and Imaging Subprogram are evaluating tyrosine kinase inhibitors, angiogenesis inhibitors and aromatase inhibitors with accompanying collaborative studies to confirm """"""""proof-of-principle"""""""" impact of therapy upon the intended targets. Novel biomarkers of early and advanced cancer are sought in bladder cancer, breast cancer, gynecologic cancers, and melanoma. New imaging technologies are being applied to identification of breast cancer lesions and primary prostate cancer, while imaging technology is applied to radiation planning for helical tomotherapy in head and neck cancer. Since the last renewal, members of Program 7 had a total of 499 publications, of which 25% were intra-programmatic and 32% were inter-programmatic.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
5P30CA044579-19
Application #
7771658
Study Section
Subcommittee G - Education (NCI)
Project Start
Project End
Budget Start
2009-02-01
Budget End
2010-01-31
Support Year
19
Fiscal Year
2009
Total Cost
$47,103
Indirect Cost
Name
University of Virginia
Department
Type
DUNS #
065391526
City
Charlottesville
State
VA
Country
United States
Zip Code
22904
Cruickshanks, Nichola; Zhang, Ying; Hine, Sarah et al. (2018) Discovery and Therapeutic Exploitation of Mechanisms of Resistance to MET Inhibitors in Glioblastoma. Clin Cancer Res :
Balogh, Kristen N; Templeton, Dennis J; Cross, Janet V (2018) Macrophage Migration Inhibitory Factor protects cancer cells from immunogenic cell death and impairs anti-tumor immune responses. PLoS One 13:e0197702
Gonzalez, Phillippe P; Kim, Jungeun; Galvao, Rui Pedro et al. (2018) p53 and NF 1 loss plays distinct but complementary roles in glioma initiation and progression. Glia 66:999-1015
Rodriguez, Anthony B; Peske, J David; Engelhard, Victor H (2018) Identification and Characterization of Tertiary Lymphoid Structures in Murine Melanoma. Methods Mol Biol 1845:241-257
Stowman, Anne M; Hickman, Alexandra W; Mauldin, Ileana S et al. (2018) Lymphoid aggregates in desmoplastic melanoma have features of tertiary lymphoid structures. Melanoma Res 28:237-245
Melhuish, Tiffany A; Kowalczyk, Izabela; Manukyan, Arkadi et al. (2018) Myt1 and Myt1l transcription factors limit proliferation in GBM cells by repressing YAP1 expression. Biochim Biophys Acta Gene Regul Mech 1861:983-995
Kulling, Paige M; Olson, Kristine C; Olson, Thomas L et al. (2018) Calcitriol-mediated reduction in IFN-? output in T cell large granular lymphocytic leukemia requires vitamin D receptor upregulation. J Steroid Biochem Mol Biol 177:140-148
Carlton, Anne L; Illendula, Anuradha; Gao, Yan et al. (2018) Small molecule inhibition of the CBF?/RUNX interaction decreases ovarian cancer growth and migration through alterations in genes related to epithelial-to-mesenchymal transition. Gynecol Oncol 149:350-360
Borten, Michael A; Bajikar, Sameer S; Sasaki, Nobuo et al. (2018) Automated brightfield morphometry of 3D organoid populations by OrganoSeg. Sci Rep 8:5319
Olson, Kristine C; Kulling Larkin, Paige M; Signorelli, Rossana et al. (2018) Vitamin D pathway activation selectively deactivates signal transducer and activator of transcription (STAT) proteins and inflammatory cytokine production in natural killer leukemic large granular lymphocytes. Cytokine 111:551-562

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