The primary mission of the Human Tissue Acquisition and Pathology Shared Resource (HTAP) is to provide Vanderbilt Cancer Center investigators with access to human tissue for the purpose of carrying out translational research. There are two main components to this Shared Resource: 1) human tissue procurement, and 2) research histology. Each of these components provides critical reagents that allow basic and applied scientific investigations of human tissues with appropriate attention to ethical concerns. Our mission is facilitated by our highly experienced personnel and a close working relationship with the Anatomic Pathology Division of the Department of Pathology. Dr. Jensen has an NCI-funded program of investigation and is an attending physician in Pathology. Ms. Newsom-Johnson worked in the Department of Pathology for over 15 years. Therefore the personnel that staff the Shared Resource have a keen appreciation of the needs of cancer researchers and are very knowledgeable concerning the need for appropriate evaluation of clinical specimens. The HTAP Shared Resource has experienced substantial growth over the last three years and has served 42 different investigators 23 of whom are Cancer Center members. During this period we have provided approximately 24,000 slides, 3,000 blocks, and provided 2,000 frozen specimens to the Vanderbilt research community. We expect continued growth for the next several years and we are in the process of adding additional personnel to keep up with the increased demand for our services. Also, due to the expressed interests from a number of Cancer Center investigators we are adding a microdissection service to the Shared Resource that will enable investigators to carefully separate tumor and normal cells for genetic and biochemical analysis.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
3P30CA068485-05S1
Application #
6398923
Study Section
Subcommittee E - Prevention &Control (NCI)
Project Start
2000-09-01
Project End
2001-08-31
Budget Start
Budget End
Support Year
5
Fiscal Year
2000
Total Cost
Indirect Cost
Name
Vanderbilt University Medical Center
Department
Type
DUNS #
004413456
City
Nashville
State
TN
Country
United States
Zip Code
37203
Bloodworth, Melissa H; Rusznak, Mark; Pfister, Connor C et al. (2018) Glucagon-like peptide 1 receptor signaling attenuates respiratory syncytial virus-induced type 2 responses and immunopathology. J Allergy Clin Immunol 142:683-687.e12
Saito-Diaz, Kenyi; Benchabane, Hassina; Tiwari, Ajit et al. (2018) APC Inhibits Ligand-Independent Wnt Signaling by the Clathrin Endocytic Pathway. Dev Cell 44:566-581.e8
Cardin, Dana B; Thota, Ramya; Goff, Laura W et al. (2018) A Phase II Study of Ganetespib as Second-line or Third-line Therapy for Metastatic Pancreatic Cancer. Am J Clin Oncol 41:772-776
Hormuth 2nd, David A; Weis, Jared A; Barnes, Stephanie L et al. (2018) Biophysical Modeling of In Vivo Glioma Response After Whole-Brain Radiation Therapy in a Murine Model of Brain Cancer. Int J Radiat Oncol Biol Phys 100:1270-1279
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
Dutter, Brendan F; Ender, Anna; Sulikowski, Gary A et al. (2018) Rhodol-based thallium sensors for cellular imaging of potassium channel activity. Org Biomol Chem 16:5575-5579
Vierra, Nicholas C; Dickerson, Matthew T; Jordan, Kelli L et al. (2018) TALK-1 reduces delta-cell endoplasmic reticulum and cytoplasmic calcium levels limiting somatostatin secretion. Mol Metab 9:84-97
Schlegel, Cameron; Weis, Victoria G; Knowles, Byron C et al. (2018) Apical Membrane Alterations in Non-intestinal Organs in Microvillus Inclusion Disease. Dig Dis Sci 63:356-365
Lewis Jr, James S; Shelton, Jeremy; Kuhs, Krystle Lang et al. (2018) p16 Immunohistochemistry in Oropharyngeal Squamous Cell Carcinoma Using the E6H4 Antibody Clone: A Technical Method Study for Optimal Dilution. Head Neck Pathol 12:440-447
Werfel, Thomas A; Wang, Shan; Jackson, Meredith A et al. (2018) Selective mTORC2 Inhibitor Therapeutically Blocks Breast Cancer Cell Growth and Survival. Cancer Res 78:1845-1858

Showing the most recent 10 out of 2462 publications