-Translational Pathology (TP) Shared Resource The Translational Pathology (TP) is a valuable resource for all aspects of experimental pathology for Cancer Center members conducting basic, translational, and clinical cancer research. The TP combines two successful LCCC cores under joint management, the Animal Histopathology Core, serving pre-clinical researchers utilizing animal models, and the Translational Pathology Laboratory, serving clinical researchers utilizing archival patient tissues from the TPF and UNC Hospitals. The TP adds value to the Cancer Center by offering its investigators competitive pricing on a wide range of histopathology services at an on -campus location with convenient access to expert pathology consultation. The Core is co-directed by Faculty Directors Ryan Miller, MD, PhD, and Stephanie Montgomery, DVM, PhD, who together have expertise in human and animal diseases, along with the guidance and experience of Facility Directors Nana Nikolaishvili Feinberg, PhD, and Dawud Hilliard. Dr. Bernand Weismann has been leading the Animal Histopathology component on an interim basis since Dr. Roger?s departure. The Core staff provides a wide range of histology services, including tissue embedding and sectioning (frozen and paraffin), routine and special histologic stains, consultation on study design and tissue collection, tissue microarray (TMA) design and construction, single and multiplex immunohistochemistry, RNA in situ hybridization (ISH), and advanced digital pathology services. During the last grant cycle, the Core has grown with added services and personnel, driven by increased NIH funding awarded to UNC investigators, expanded on-campus animal housing facilities, and the maturation of large on-campus initiatives, including the Collaborative Cross and Mouse Phase 1 Unit. During the next funding period, the TP will expand available services and technologies to meet the demands of Cancer Center investigators, including advancing available animal immunohistochemistry and immunofluorescence reagents, developing FISH assay using commercially available PNA (peptide nucleic acid) and LSI/CEP probes, and acquiring a new state-of ?the-art fluorescent scanner with higher speed, capacity, and magnification for scanning of IF and FISH slides. Accordingly, we request an increased budget of $216,836 representing 5% of the total TP budget to promote expanded utilization and capabilities.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
5P30CA016086-44
Application #
9834862
Study Section
Subcommittee I - Transistion to Independence (NCI)
Project Start
Project End
Budget Start
2019-12-01
Budget End
2020-11-30
Support Year
44
Fiscal Year
2020
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