Pathology Shared Resource (PSR) The Pathology Shared Resource (PSR) was created to provide Norris Cotton Cancer Center (NCCC) investigators from different backgrounds (e.g., physicians, basic scientists, diagnosticians) access to a CLIA- certified, CAP-accredited facility with standardized laboratory protocols for histologic, quantitative imaging and molecular analysis. The ultimate goal of the PSR is to provide NCCC investigators with state-of-the-art technical and professional support leading to quality results for clinical and pre-clinical studies. The PSR has consolidated institutional expertise and experience by combining responsibility for providing for and supporting both clinical and research utilization of these services. The PSR supports human tissue and cell procurement/acquisition (i.e., handling, storage, distribution and biobanking); histology and immunohistochemical analysis; molecular pathology analysis (i.e., genotyping, next-generation sequencing, quantitative PCR, tissue microarrays; cell processing services); and cytogenetics analysis. The PSR is directed by Dr. Gregory Tsongalis, who oversees a staff of 12 that includes two Research Associates, two Histotechnologists, an Apheresis Nurse, and seven additional technical specialists. The PSR is organized to identify as early as possible the needs of researchers in developing and supporting their translational research project, providing them with technical support and consultation. Further, many Pathology faculty become involved in collaborating on individual research projects by reviewing proposals, selecting appropriate tissues, designing IHC staining and molecular testing algorithms, creating tissue arrays, suggesting alternative biomarker testing, and scoring IHC expression levels. The PSR has supported NCCC Members in each of the six Research Programs: Cancer Control (2 members), Cancer Epidemiology (6 members), Cancer Mechanisms (12 members), Molecular Therapeutics (27 members), Cancer Imaging & Radiobiology (7 members), and Immunology & Cancer Immunotherapy (12 members).

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
5P30CA023108-40
Application #
9616821
Study Section
Subcommittee I - Transistion to Independence (NCI)
Project Start
Project End
Budget Start
2018-12-01
Budget End
2019-11-30
Support Year
40
Fiscal Year
2019
Total Cost
Indirect Cost
Name
Dartmouth College
Department
Type
DUNS #
041027822
City
Hanover
State
NH
Country
United States
Zip Code
03755
Rodriguez-Garcia, Marta; Fortier, Jared M; Barr, Fiona D et al. (2018) Aging impacts CD103+ CD8+ T cell presence and induction by dendritic cells in the genital tract. Aging Cell 17:e12733
Shajani-Yi, Zahra; de Abreu, Francine B; Peterson, Jason D et al. (2018) Frequency of Somatic TP53 Mutations in Combination with Known Pathogenic Mutations in Colon Adenocarcinoma, Non-Small Cell Lung Carcinoma, and Gliomas as Identified by Next-Generation Sequencing. Neoplasia 20:256-262
Shee, Kevin; Jiang, Amanda; Varn, Frederick S et al. (2018) Cytokine sensitivity screening highlights BMP4 pathway signaling as a therapeutic opportunity in ER+ breast cancer. FASEB J :fj201801241R
Bossé, Yohan; Amos, Christopher I (2018) A Decade of GWAS Results in Lung Cancer. Cancer Epidemiol Biomarkers Prev 27:363-379
Pande, Mala; Joon, Aron; Brewster, Abenaa M et al. (2018) Genetic susceptibility markers for a breast-colorectal cancer phenotype: Exploratory results from genome-wide association studies. PLoS One 13:e0196245
Szczepiorkowski, Zbigniew M; Burnett, Christine A; Dumont, Larry J et al. (2018) Apheresis buffy coat collection without photoactivation has no effect on apoptosis, cell proliferation, and total viability of mononuclear cells collected using photopheresis systems. Transfusion 58:943-950
Gorlova, Olga Y; Li, Yafang; Gorlov, Ivan et al. (2018) Gene-level association analysis of systemic sclerosis: A comparison of African-Americans and White populations. PLoS One 13:e0189498
Schmit, Stephanie L; Edlund, Christopher K; Schumacher, Fredrick R et al. (2018) Novel Common Genetic Susceptibility Loci for Colorectal Cancer. J Natl Cancer Inst :
Smith, T Jarrod; Sondermann, Holger; O'Toole, George A (2018) Co-opting the Lap System of Pseudomonas fluorescens To Reversibly Customize Bacterial Cell Surfaces. ACS Synth Biol 7:2612-2617
Trentham-Dietz, Amy; Ergun, Mehmet Ali; Alagoz, Oguzhan et al. (2018) Comparative effectiveness of incorporating a hypothetical DCIS prognostic marker into breast cancer screening. Breast Cancer Res Treat 168:229-239

Showing the most recent 10 out of 1911 publications