The specific aims of this proposal are 1)To collect, process, bank and distribute human colorectal neoplasms and matched normal tissue samples to investigators in the Vanderbilt Gl SPORE and other Gl SPORES; 2)To collect and bank portions of polyps and biopsies of grossly normal colorectal mucosa to facilitate research in adenoma recurrence;3)To perform quality control to ensure that the relevant tissue is supplied to the researcher and that tissues are suitable for the planned research (not necrotic or involved by unsuspected disease processes);4)To protect patient confidentiality through use of an explicit consent form that specifically addresses use of extraneous tissue for research purposes and through de-identification of specimens;5)To work with the Biostatistics/Bioinformatics Core to establish an informatics strategy for networking of requests, specimen tracking, extraction of de-identified data relating to specimens of interest and linkage to research data. 6) To provide laser capture microdissection services to the Gl SPORE investigators;7)To provide tissue microarray services to the Gl SPORE investigators and provide TMA slides to investigators at other institutions (such as the H. Lee Moffitt Cancer Center) and other Gl SPOREs;8)To provide expertise in evaluation of histopathology of mouse models of colorectal neoplasia and correlation with human disease;10)To provide expertise in developing, performing and evaluating immunohistochemical stains for Gl SPORE investigators. The Gl SPORE Tissue Core at VUMC has partnered with other mechanisms for tissue collection at VUMC under Dr. Washington's direction: the Human Tissue Acquisition and Pathology Shared Resource of the Vanderbilt-lngram Comprehensive Cancer Center, the Tissue Morphology SubCore for the Digestive Disease Research Center and the VUMC-led Western Division of the Cooperative Human Tissue Network. Mechanisms and standard operating procedures for collection of human Gl tissue, quality assurance and immunohistochemistry have been used to support all five SPORE projects in the previous funding period. By partnering with other tissue and histology resources at VUMC, the Gl SPORE Tissue Core is able to provide high quality services to SPORE investigators in a highly cost effective manner.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Specialized Center (P50)
Project #
5P50CA095103-09
Application #
8073540
Study Section
Special Emphasis Panel (ZCA1)
Project Start
Project End
Budget Start
2010-05-01
Budget End
2011-04-30
Support Year
9
Fiscal Year
2010
Total Cost
$157,484
Indirect Cost
Name
Vanderbilt University Medical Center
Department
Type
DUNS #
004413456
City
Nashville
State
TN
Country
United States
Zip Code
37212
Means, Anna L; Freeman, Tanner J; Zhu, Jing et al. (2018) Epithelial Smad4 Deletion Up-Regulates Inflammation and Promotes Inflammation-Associated Cancer. Cell Mol Gastroenterol Hepatol 6:257-276
Weiss, Vivian L; Kiernan, Colleen; Wright, Jesse et al. (2018) Fine-Needle Aspiration-Based Grading of Pancreatic Neuroendocrine Neoplasms Using Ki-67: Is Accurate WHO Grading Possible on Cytologic Material? J Am Soc Cytopathol 7:154-459
Roberts, Jordan; Gonzalez, Raul S; Revetta, Frank et al. (2018) Mesenteric tumour deposits arising from small-intestine neuroendocrine tumours are frequently associated with fibrosis and IgG4-expressing plasma cells. Histopathology 73:795-800
Gibson, William E; Gonzalez, Raul S; Cates, Justin M M et al. (2018) Hepatic micrometastases are associated with poor prognosis in patients with liver metastases from neuroendocrine tumors of the digestive tract. Hum Pathol 79:109-115
Fenix, Aidan M; Neininger, Abigail C; Taneja, Nilay et al. (2018) Muscle-specific stress fibers give rise to sarcomeres in cardiomyocytes. Elife 7:
Wang, Jing; Zhao, Yue; Zhou, Xiaofan et al. (2018) Nascent RNA sequencing analysis provides insights into enhancer-mediated gene regulation. BMC Genomics 19:633
Burns, Michael C; Howes, Jennifer E; Sun, Qi et al. (2018) High-throughput screening identifies small molecules that bind to the RAS:SOS:RAS complex and perturb RAS signaling. Anal Biochem 548:44-52
Herring, Charles A; Banerjee, Amrita; McKinley, Eliot T et al. (2018) Unsupervised Trajectory Analysis of Single-Cell RNA-Seq and Imaging Data Reveals Alternative Tuft Cell Origins in the Gut. Cell Syst 6:37-51.e9
Hinger, Scott A; Cha, Diana J; Franklin, Jeffrey L et al. (2018) Diverse Long RNAs Are Differentially Sorted into Extracellular Vesicles Secreted by Colorectal Cancer Cells. Cell Rep 25:715-725.e4
Weigl, Korbinian; Thomsen, Hauke; Balavarca, Yesilda et al. (2018) Genetic Risk Score Is Associated With Prevalence of Advanced Neoplasms in a Colorectal Cancer Screening Population. Gastroenterology 155:88-98.e10

Showing the most recent 10 out of 447 publications