The purpose of the VICC Human Tissue Acquisition and Pathology Shared Resource (HTAP) is to provide support for Cancer Center investigators engaged in translational and basic science research efforts. It provides researchers with access to a wide variety of human specimens and tissues. The objectives of HTAP are to collect, process, bank, and distribute remnant human tissues (both normal and neoplastic) from routine surgical resections and autopsies for use by peer-reviewed funded investigators of the VICC in basic, clinical, and translational research studies; provide the highest quality of well-characterized fresh, frozen, and fixed tissues suitable for a wide range of molecular, biochemical, and tissue analyses; assist with collection and banking of biopsy material for specific cancer-related clinical trials and other projects; provide, as feasible, human tissues to other peer-reviewed funded Vanderbilt University investigators who are not members of the VICC, and to newly-established investigators who have yet to receive funding; and to perform quality control to ensure that the relevant tissue is supplied to the researcher, and that tissues are suitable for the planned research (e.g., not necrotic or involved by unsuspected disease processes.) New services offered by HTAP include laser capture microscopy, tissue array block construction, and access to the BLISS automated software/imaging system. In addition, tissue collection efforts have been extensively refined and new preservation methods offered. Dr. Kay Washington is the Director of the Human Tissue Acquisition and Pathology Shared Resource and is engaged in a number of collaborative projects with VICC investigators. She is assisted by a staff with decades of experience in offering these services, and partners with the Bioinformatics Shared Resource, under the direction of Dr. Mary Edgerton, to develop easily-customized tools for specimen tracking and linkage of genomic, proteomic and biologic data to tissue specimens.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
5P30CA068485-11
Application #
7289850
Study Section
Subcommittee G - Education (NCI)
Project Start
Project End
Budget Start
2006-09-01
Budget End
2007-08-31
Support Year
11
Fiscal Year
2006
Total Cost
$134,840
Indirect Cost
Name
Vanderbilt University Medical Center
Department
Type
DUNS #
004413456
City
Nashville
State
TN
Country
United States
Zip Code
37212
Choksi, Yash A; Reddy, Vishruth K; Singh, Kshipra et al. (2018) BVES is required for maintenance of colonic epithelial integrity in experimental colitis by modifying intestinal permeability. Mucosal Immunol 11:1363-1374
Elion, David L; Cook, Rebecca S (2018) Harnessing RIG-I and intrinsic immunity in the tumor microenvironment for therapeutic cancer treatment. Oncotarget 9:29007-29017
Kook, Seunghyi; Qi, Aidong; Wang, Ping et al. (2018) Gene-edited MLE-15 Cells as a Model for the Hermansky-Pudlak Syndromes. Am J Respir Cell Mol Biol 58:566-574
Chavez, Diana A; Greer, Briana H; Eichman, Brandt F (2018) The HIRAN domain of helicase-like transcription factor positions the DNA translocase motor to drive efficient DNA fork regression. J Biol Chem 293:8484-8494
Cooke, Allison L; Morris, Jamie; Melchior, John T et al. (2018) A thumbwheel mechanism for APOA1 activation of LCAT activity in HDL. J Lipid Res 59:1244-1255
Yang, Yaohua; Cai, Qiuyin; Shu, Xiao-Ou et al. (2018) Prospective study of oral microbiome and colorectal cancer risk in low-income and African American populations. Int J Cancer :
Funkhouser-Jones, Lisa J; van Opstal, Edward J; Sharma, Ananya et al. (2018) The Maternal Effect Gene Wds Controls Wolbachia Titer in Nasonia. Curr Biol 28:1692-1702.e6
Nyhoff, Lindsay E; Clark, Emily S; Barron, Bridgette L et al. (2018) Bruton's Tyrosine Kinase Is Not Essential for B Cell Survival beyond Early Developmental Stages. J Immunol 200:2352-2361
Horvat, Andela; Noto, Jennifer M; Ramatchandirin, Balamurugan et al. (2018) Helicobacter pylori pathogen regulates p14ARF tumor suppressor and autophagy in gastric epithelial cells. Oncogene 37:5054-5065
Raybuck, Ariel L; Cho, Sung Hoon; Li, Jingxin et al. (2018) B Cell-Intrinsic mTORC1 Promotes Germinal Center-Defining Transcription Factor Gene Expression, Somatic Hypermutation, and Memory B Cell Generation in Humoral Immunity. J Immunol 200:2627-2639

Showing the most recent 10 out of 2462 publications