TRANSLATIONAL PATHOLOGY SHARED RESOURCE The TP facility is a multi-component SR that integrates human and non-human histopathology services to facilitate and coordinate studies for LCCC members. TP provides expertise and techniques focused on either pre-clinical (AHC) or clinical (TPL) specimens and facilitates translation of results between the two. Each component is led by board-certified faculty pathologist (MD, DVM, PhD) who oversees operations and long- term planning. AHC provides comprehensive animal pathology support to investigators, from study design through specimen handling, grossing, routine and specialized histologic techniques, bloodwork, urinalysis, molecular characterization of tissue, and tissue morphologic analysis. The AHC component director Stephanie Montgomery, DVM, PhD is expanding the core and its capabilities by initiating a novel training program in veterinary pathology in combination with UNC sister University NC State and its Veterinary School. TPL, under Dr. Sara Wobker, MD, supports clinical studies by providing access to formalin-fixed, paraffin-embedded tissues from UNC Hospitals Surgical Pathology archives, start-to-finish translational pathology project management, and histopathology services. Both components are equipped with instrumentation for routine pathology but have upgrades for high level digital pathology and analysis. New technology for single cell analysis including the Geo Max from Nanostring is being incorporated into the SR to aid in understanding the tumor microenvironment. The facility is well used by 109 total users of which 78 (72%) are Center members. The facility is well- supported by chargebacks, receiving 57% of their fiscal year 2019 operating revenue from that source. TP is requesting $186,872 from the CCSG or 12% of the operating budget. TP has supported 200 peer-reviewed publications during the last funding cycle of the CCSG including cancer therapeutics, immunotherapy, nutrition and cancer, nanotechnology, cancer cell signaling, gene therapy, novel cancer models, and personalized medicine.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
2P30CA016086-45
Application #
10089832
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
Lianga, Noel; Doré, Carole; Kennedy, Erin K et al. (2018) Cdk1 phosphorylation of Esp1/Separase functions with PP2A and Slk19 to regulate pericentric Cohesin and anaphase onset. PLoS Genet 14:e1007029
Allott, Emma H; Geradts, Joseph; Cohen, Stephanie M et al. (2018) Frequency of breast cancer subtypes among African American women in the AMBER consortium. Breast Cancer Res 20:12
Dhungel, Bal Mukunda; Montgomery, Nathan D; Painschab, Matthew S et al. (2018) 'Discovering' primary effusion lymphoma in Malawi. AIDS 32:2264-2266
Cameron, Jennifer E; Rositch, Anne F; Vielot, Nadja A et al. (2018) Epstein-Barr Virus, High-Risk Human Papillomavirus and Abnormal Cervical Cytology in a Prospective Cohort of African Female Sex Workers. Sex Transm Dis 45:666-672
Lim, Joseph K; Liapakis, Ann Marie; Shiffman, Mitchell L et al. (2018) Safety and Effectiveness of Ledipasvir and Sofosbuvir, With or Without Ribavirin, in Treatment-Experienced Patients With Genotype 1 Hepatitis C Virus Infection and Cirrhosis. Clin Gastroenterol Hepatol 16:1811-1819.e4
Wang, Gary P; Terrault, Norah; Reeves, Jacqueline D et al. (2018) Prevalence and impact of baseline resistance-associated substitutions on the efficacy of ledipasvir/sofosbuvir or simeprevir/sofosbuvir against GT1 HCV infection. Sci Rep 8:3199
Phillips, Bonnie; Van Rompay, Koen K A; Rodriguez-Nieves, Jennifer et al. (2018) Adjuvant-Dependent Enhancement of HIV Env-Specific Antibody Responses in Infant Rhesus Macaques. J Virol 92:
Takaku, Motoki; Grimm, Sara A; Roberts, John D et al. (2018) GATA3 zinc finger 2 mutations reprogram the breast cancer transcriptional network. Nat Commun 9:1059
Galanis, Evanthia; Anderson, S Keith; Miller, C Ryan et al. (2018) Phase I/II trial of vorinostat combined with temozolomide and radiation therapy for newly diagnosed glioblastoma: results of Alliance N0874/ABTC 02. Neuro Oncol 20:546-556
Agle, Kimberle; Vincent, Benjamin G; Piper, Clint et al. (2018) Bim regulates the survival and suppressive capability of CD8+ FOXP3+ regulatory T cells during murine GVHD. Blood 132:435-447

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