-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 #
5P30CA016086-42
Application #
9391973
Study Section
Subcommittee I - Transistion to Independence (NCI)
Project Start
Project End
Budget Start
2017-12-01
Budget End
2018-11-30
Support Year
42
Fiscal Year
2018
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
Thomas, Nancy E; Edmiston, Sharon N; Tsai, Yihsuan S et al. (2018) Utility of TERT Promoter Mutations for Cutaneous Primary Melanoma Diagnosis. Am J Dermatopathol :
Bensen, Jeannette T; Graff, Mariaelisa; Young, Kristin L et al. (2018) A survey of microRNA single nucleotide polymorphisms identifies novel breast cancer susceptibility loci in a case-control, population-based study of African-American women. Breast Cancer Res 20:45
Hall, Marissa G; Marteau, Theresa M; Sunstein, Cass R et al. (2018) Public support for pictorial warnings on cigarette packs: an experimental study of US smokers. J Behav Med 41:398-405
Ma, Shaohua; Paiboonrungruan, Chorlada; Yan, Tiansheng et al. (2018) Targeted therapy of esophageal squamous cell carcinoma: the NRF2 signaling pathway as target. Ann N Y Acad Sci 1434:164-172
Aung, Kyaw L; Fischer, Sandra E; Denroche, Robert E et al. (2018) Genomics-Driven Precision Medicine for Advanced Pancreatic Cancer: Early Results from the COMPASS Trial. Clin Cancer Res 24:1344-1354
Suh, Junghyun L; Watts, Brian; Stuckey, Jacob I et al. (2018) Quantitative Characterization of Bivalent Probes for a Dual Bromodomain Protein, Transcription Initiation Factor TFIID Subunit 1. Biochemistry 57:2140-2149
Brock, William J; Beaudoin, James J; Slizgi, Jason R et al. (2018) Bile Acids as Potential Biomarkers to Assess Liver Impairment in Polycystic Kidney Disease. Int J Toxicol 37:144-154
Lindström, Linda S; Yau, Christina; Czene, Kamila et al. (2018) Intratumor Heterogeneity of the Estrogen Receptor and the Long-term Risk of Fatal Breast Cancer. J Natl Cancer Inst 110:726-733
Jayasinghe, Reyka G; Cao, Song; Gao, Qingsong et al. (2018) Systematic Analysis of Splice-Site-Creating Mutations in Cancer. Cell Rep 23:270-281.e3
Parr, Jonathan B; Lodge, Evans K; Holzmayer, Vera et al. (2018) An Efficient, Large-Scale Survey of Hepatitis C Viremia in the Democratic Republic of the Congo Using Dried Blood Spots. Clin Infect Dis 66:254-260

Showing the most recent 10 out of 1525 publications