Identification of critical changes in gene expression that are responsible for the malignant phenotype haslong been the goal of biomedical researchers in the basic and clinical sciences. Much has been learnedconcerning disease mechanism using model systems (tissue culture and animals) but the translation offindings in model systems to human clinical disease has been less than optimal. The latter is due at least inpart to the complexity of human clinical disease which results from the vast number of genes which areactive in cellular metabolism and the co-morbidities associated with an individual patient's disease which canalter or bias the phenotype of the disease process. The development of high throughput testing methodssuch as DMA chip technologies for measuring gene expression, chromosomal hybridization and singlenucleotide polymporphisms has in part addressed the issue of biological complexity at the cellular level.However, acquiring clinical co-morbidity and treatment data that is likely to affect patient outcome and mayimpact changes in cellular metabolism is more difficult as it relies on various manual human recording andreporting systems.The Tissue and Data Acquisition and Analysis Core (TDAAC) has as its goal the acquisition of humanspecimens and associated clinical and pathologic findings to support translational research of the targetdisease. To this end it supports an IRB approved protocol 'Tissue Acquisition System to Support CancerResearch' (TASSCR) as well as other investigator initiated IRB approved protocols to support specificinvestigative questions. Because TDAAC is an outgrowth of a multicenter grant that focused on geneexpression microarray studies on multiple cancer phenotypes, some samples have associated geneexpression data as a part of their annotation. TDAAC faculty and staff support translational research throughacquisition of annotated tissue and blood samples under high ethical standards utilizing patient informedconsent and treatment of specimens such that the primary purpose of the specimen for patient care ismaintained and the quality of the specimen is optimal for biomedical research.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
2P30CA016059-28
Application #
7698825
Study Section
Subcommittee G - Education (NCI)
Project Start
2008-09-03
Project End
2011-04-30
Budget Start
2008-09-03
Budget End
2009-04-30
Support Year
28
Fiscal Year
2008
Total Cost
$24,028
Indirect Cost
Name
Virginia Commonwealth University
Department
Type
DUNS #
105300446
City
Richmond
State
VA
Country
United States
Zip Code
23298
Yamada, Akimitsu; Nagahashi, Masayuki; Aoyagi, Tomoyoshi et al. (2018) ABCC1-Exported Sphingosine-1-phosphate, Produced by Sphingosine Kinase 1, Shortens Survival of Mice and Patients with Breast Cancer. Mol Cancer Res 16:1059-1070
Cantwell, Marc T; Farrar, Jared S; Lownik, Joseph C et al. (2018) STAT3 suppresses Wnt/?-catenin signaling during the induction phase of primary Myf5+ brown adipogenesis. Cytokine 111:434-444
Aqbi, Hussein F; Wallace, Matthew; Sappal, Samay et al. (2018) IFN-? orchestrates tumor elimination, tumor dormancy, tumor escape, and progression. J Leukoc Biol :
Volker, Sonja E; Hedrick, Shannon E; Feeney, Yvonne B et al. (2018) Cyclophilin A Function in Mammary Epithelium Impacts Jak2/Stat5 Signaling, Morphogenesis, Differentiation, and Tumorigenesis in the Mammary Gland. Cancer Res 78:3877-3887
Li, Xiaojiaoyang; Liu, Runping; Huang, Zhiming et al. (2018) Cholangiocyte-derived exosomal long noncoding RNA H19 promotes cholestatic liver injury in mouse and humans. Hepatology 68:599-615
Durant, Stephen T; Zheng, Li; Wang, Yingchun et al. (2018) The brain-penetrant clinical ATM inhibitor AZD1390 radiosensitizes and improves survival of preclinical brain tumor models. Sci Adv 4:eaat1719
Damle, S R; Martin, R K; Cockburn, C L et al. (2018) ADAM10 and Notch1 on murine dendritic cells control the development of type 2 immunity and IgE production. Allergy 73:125-136
Wang, Feng; Li, Hongyan; Markovsky, Ela et al. (2018) Pazopanib radio-sensitization of human sarcoma tumors. Oncotarget 9:9311-9324
Stokes, Nancy A; Stanciu, Cristina E; Brocato, Emily R et al. (2018) Simplification of complex DNA profiles using front end cell separation and probabilistic modeling. Forensic Sci Int Genet 36:205-212
Poklepovic, Andrew; Qu, Yuesheng; Dickinson, Molly et al. (2018) Randomized study of doxorubicin-based chemotherapy regimens, with and without sildenafil, with analysis of intermediate cardiac markers. Cardiooncology 4:

Showing the most recent 10 out of 586 publications