The Histopathology & Tissue Shared Resource (HTSR) is the Georgetown Lombardi Comprehensive Cancer Center (LCCC) resource for accessing human tissue for translational research and provides comprehensive, high-quality laboratory and interpretive pathology services. The HTSR collects and distributes fresh, frozen and formalin-fixed, paraffin-embedded tissues (10,773 patients consented to date) and supplies technical and pathology support for investigator-driven collection protocols, including the novel conditionally reprogrammed cells (CRCs) and zevatar projects. HTSR Codirector Brent Harris, MD, PhD, oversees the delivery of HTSR?s comprehensive pathology services related to human and animal tissues. Under the day-to-day management of Codirector Deborah Berry, PhD, the laboratory provides human tissue and liquid biospecimens for translational research projects and comprehensive histology services, including tissue processing, paraffin and frozen section microtomy, staining, immunohistochemistry (IHC), immunofluorescence, laser-capture microdissection and tissue microarray (TMA) construction, staining and interpretative analysis. The HTSR also offers expert bioinformatics technical support, pathology database search capabilities, consultation services and educational support and training for users. In response to user surveys, investigator feedback and Advisory Committee recommendations since the last review, the HTSR has expanded its services to include quantitative automated brightfield and immunofluorescence image analysis, immunophenotyping, microRNA (miRNA) in situ staining and TMA construction. The HTSR works cooperatively with the Genomics & Epigenomics Shared Resource (GESR) and the Proteomics & Metabolomics Shared Resource (PMSR) to prepare human and animal model tissues for downstream genomic, proteomic and metabolomic analysis. The HTSR works cooperatively with the Biostatistics & Bioinformatics Shared Resource (BBSR) to document clinical information and patient outcomes comprehensively for samples distributed from the HTSR, including specimens collected by the Survey, Recruitment & Biospecimen Collection Shared Resource (SRBSR) and Indivumed GmbH. Forty peer review? funded LCCC investigators representing all four LCCC Research Programs (Breast Cancer [BC], Cancer Prevention and Control [CPC], Experimental Therapeutics [ET], and Molecular Oncology [MO]) used the HTSR in 2017. The impact of the HTSR is demonstrated by the 70 peer-reviewed publications that have used HTSR resources in the current funding period.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
5P30CA051008-27
Application #
9924513
Study Section
Subcommittee I - Transistion to Independence (NCI)
Project Start
Project End
Budget Start
2020-05-01
Budget End
2021-04-30
Support Year
27
Fiscal Year
2020
Total Cost
Indirect Cost
Name
Georgetown University
Department
Type
DUNS #
049515844
City
Washington
State
DC
Country
United States
Zip Code
20057
Lee, Yichien; Rodriguez, Olga C; Albanese, Chris et al. (2018) Divergent brain changes in two audiogenic rat strains: A voxel-based morphometry and diffusion tensor imaging comparison of the genetically epilepsy prone rat (GEPR-3) and the Wistar Audiogenic Rat (WAR). Neurobiol Dis 111:80-90
Coia, Heidi; Ma, Ning; Hou, Yanqi et al. (2018) Prevention of Lipid Peroxidation-derived Cyclic DNA Adduct and Mutation in High-Fat Diet-induced Hepatocarcinogenesis by Theaphenon E. Cancer Prev Res (Phila) 11:665-676
Ory, Virginie; Kietzman, William B; Boeckelman, Jacob et al. (2018) The PPAR? agonist efatutazone delays invasive progression and induces differentiation of ductal carcinoma in situ. Breast Cancer Res Treat 169:47-57
Ozawa, Patricia Midori Murobushi; Alkhilaiwi, Faris; Cavalli, Iglenir João et al. (2018) Extracellular vesicles from triple-negative breast cancer cells promote proliferation and drug resistance in non-tumorigenic breast cells. Breast Cancer Res Treat 172:713-723
Smith, Jill P; Wang, Shangzi; Nadella, Sandeep et al. (2018) Cholecystokinin receptor antagonist alters pancreatic cancer microenvironment and increases efficacy of immune checkpoint antibody therapy in mice. Cancer Immunol Immunother 67:195-207
Edwardson, Matthew A; Zhong, Xiaogang; Fiandaca, Massimo S et al. (2018) Plasma microRNA markers of upper limb recovery following human stroke. Sci Rep 8:12558
Kaat, Aaron J; Schalet, Benjamin D; Rutsohn, Joshua et al. (2018) Physical function metric over measure: An illustration with the Patient-Reported Outcomes Measurement Information System (PROMIS) and the Functional Assessment of Cancer Therapy (FACT). Cancer 124:153-160
Maximov, Philipp Y; Abderrahman, Balkees; Fanning, Sean W et al. (2018) Endoxifen, 4-Hydroxytamoxifen and an Estrogenic Derivative Modulate Estrogen Receptor Complex Mediated Apoptosis in Breast Cancer. Mol Pharmacol 94:812-822
Czarnecka, Magdalena; Lu, Congyi; Pons, Jennifer et al. (2018) Neuropeptide Y receptor interactions regulate its mitogenic activity. Neuropeptides :
Gonzalez, Thomas L; Moos, Rebecca K; Gersch, Christina L et al. (2018) Metabolites of n-Butylparaben and iso-Butylparaben Exhibit Estrogenic Properties in MCF-7 and T47D Human Breast Cancer Cell Lines. Toxicol Sci 164:50-59

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