CLINICAL AND TRANSLATIONAL RESEARCH PROGRAM Recognizing the fundamental nature of clinical research at UNC, and that common vulnerabilities may be found across many cancers, CR has further invested in the bench-to-bedside continuum. We have become even more integrated around the themes of tissue-based research, novel therapeutics and technologies with a pivot towards investigator intiated trials (IITs). CR, rated ?Outstanding? at the last competitive renewal, has broad clinical and research expertise across all cancer types and key correlative strengths in imaging, statistical design, biomarker development, immuno-oncology, and tissue-based research. CR themes include: 1) Develop and evaluate novel therapies through early phase and investigator-initiated clinical trials; 2) Conduct tissue-based state-of-the-art ?omics research to improve cancer treatments; 3) Develop new technologies for the diagnosis and treatment of cancer. Highlights of CR work and future plans include innovative IITs leveraging UNC research, an investment and track record of success in cellular immunotherapy trials, translating genomics efforts into therapeutic clinical trials, and incorporating biomarker development, novel imaging, and technologies into our trials. It is led by three dynamic trialists and physician-scientists, Drs. Dees, Milowsky, and Yeh. Each bring a complementary skill set to the program: Early Phase trials (Dees), genomics and novel drug trials (Milowsky), and translational collaborative research (Yeh). CR focuses on catchment area diseases and on training the next generation of clinical scientists. CR members are involved in multiple trials targeting cancers of particular relevance to the catchment area, the state of North Carolina. The CR Program consists of 60 members who are associated with 7 basic science and 10 clinical departments at UNC-Chapel Hill and affiliated institutions. During the last funding period, members published 1260 cancer- related articles, 34% were inter-programmatic and 18% were intra-programmatic (45% collaborative). In 2019, program members held grants totaling $18.7M (direct cost) in cancer-relevant extramural funding, including $5.2M (direct costs) from the NCI and $4.9M other peer-reviewed funding.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
2P30CA016086-45
Application #
10089816
Study Section
Subcommittee I - Transistion to Independence (NCI)
Project Start
1997-06-01
Project End
2025-11-30
Budget Start
2020-12-01
Budget End
2021-11-30
Support Year
45
Fiscal Year
2021
Total Cost
Indirect Cost
Name
University of North Carolina Chapel Hill
Department
Type
DUNS #
608195277
City
Chapel Hill
State
NC
Country
United States
Zip Code
27599
Anderson, Chelsea; Smitherman, Andrew B; Nichols, Hazel B (2018) Conditional relative survival among long-term survivors of adolescent and young adult cancers. Cancer 124:3037-3043
Liu, Meng-Xi; Jin, Lei; Sun, Si-Jia et al. (2018) Metabolic reprogramming by PCK1 promotes TCA cataplerosis, oxidative stress and apoptosis in liver cancer cells and suppresses hepatocellular carcinoma. Oncogene 37:1637-1653
Curtis 2nd, Alan D; Jensen, Kara; Van Rompay, Koen K A et al. (2018) A simultaneous oral and intramuscular prime/sublingual boost with a DNA/Modified Vaccinia Ankara viral vector-based vaccine induces simian immunodeficiency virus-specific systemic and mucosal immune responses in juvenile rhesus macaques. J Med Primatol 47:288-297
Williams, Lindsay A; Nichols, Hazel B; Hoadley, Katherine A et al. (2018) Reproductive risk factor associations with lobular and ductal carcinoma in the Carolina Breast Cancer Study. Cancer Causes Control 29:25-32
Amunugama, Ravindra; Willcox, Smaranda; Wu, R Alex et al. (2018) Replication Fork Reversal during DNA Interstrand Crosslink Repair Requires CMG Unloading. Cell Rep 23:3419-3428
Little, Michael S; Pellock, Samuel J; Walton, William G et al. (2018) Structural basis for the regulation of ?-glucuronidase expression by human gut Enterobacteriaceae. Proc Natl Acad Sci U S A 115:E152-E161
Knott, Simon R V; Wagenblast, Elvin; Khan, Showkhin et al. (2018) Erratum: Asparagine bioavailability governs metastasis in a model of breast cancer. Nature 556:135
Dellon, Evan S; Selitsky, Sara R; Genta, Robert M et al. (2018) Gene expression-phenotype associations in adults with eosinophilic esophagitis. Dig Liver Dis 50:804-811
Rojas, Juan D; Lin, Fanglue; Chiang, Yun-Chen et al. (2018) Ultrasound Molecular Imaging of VEGFR-2 in Clear-Cell Renal Cell Carcinoma Tracks Disease Response to Antiangiogenic and Notch-Inhibition Therapy. Theranostics 8:141-155
Chai, Zheng; Zhang, Xintao; Rigsbee, Kelly Michelle et al. (2018) Cryoprecipitate augments the global transduction of the adeno-associated virus serotype 9 after a systemic administration. J Control Release 286:415-424

Showing the most recent 10 out of 1525 publications