Each research project within this COBRE application relies heavily on gene expression analysis for the completion of their specific aims. The most common genomic approaches in this application are gene expression profiling by microarray, single mRNA measurement abundance by real-time PCR, and DNA sequencing and sequence analysis. Microarray experimentation and DNA sequencing require expensive instrumentation and reagents, sophisticated methods, and intense data management and analysis. These tasks are most efficiently executed by core facility personnel. The proposed COBRE projects cannot be completed without direct access to expert genomic technical and analytical support. Therefore, the objective of this application is to implement a Genomic Core Facility that will serve the specific needs of the COBRE and Marshall University investigations in the areas of microarray-based gene expression profiling, real-time PCR, automated DNA sequencing and DNA sequence analysis. Both the microarray manager and genomic data analyst will require substantial external training to keep pace with developments and provide useful analyses for the end users. The long-term goal of the Genomics Core Facility is to position COBRE investigators to discover novel molecular pathways in cancer development. We will enable the genomic research goals of the COBRE research projects by pursuing the following two specific aims: 1. Implement a Genomics Core Facility and develop Microarray Data Analysis capabilities. The Genomic Core Facility will be co-directed by Drs Niles and Primerano who have complementary skills in experimental design and core management. Given the experience of the co-directors and presence of key personnel and instrumentation, we are well prepared to develop the Genomics Core Facility. It is our expectation that the Genomics Core Facility will enable COBRE and Marshall University investigators to identify candidate genes that are critically involved in cell signal transduction, confirm pattems of expression, and gain insights into cancer molecular biology.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Exploratory Grants (P20)
Project #
1P20RR020180-01
Application #
6973105
Study Section
Special Emphasis Panel (ZRR1-RI-5 (01))
Project Start
2004-09-23
Project End
2005-07-31
Budget Start
2004-09-23
Budget End
2005-07-31
Support Year
1
Fiscal Year
2004
Total Cost
$495,370
Indirect Cost
Name
Marshall University
Department
Biochemistry
Type
Schools of Medicine
DUNS #
036156615
City
Huntington
State
WV
Country
United States
Zip Code
25701
Abbas, Ata; Hall, J Adam; Patterson 3rd, William L et al. (2016) Sulforaphane modulates telomerase activity via epigenetic regulation in prostate cancer cell lines. Biochem Cell Biol 94:71-81
Silvis, Anne M; McCormick, Michael L; Spitz, Douglas R et al. (2016) Redox balance influences differentiation status of neuroblastoma in the presence of all-trans retinoic acid. Redox Biol 7:88-96
Valentovic, Monica A; Ball, John G; Brown, J Mike et al. (2014) Resveratrol attenuates cisplatin renal cortical cytotoxicity by modifying oxidative stress. Toxicol In Vitro 28:248-57
Mathis, Sarah E; Alberico, Anthony; Nande, Rounak et al. (2014) Chemo-predictive assay for targeting cancer stem-like cells in patients affected by brain tumors. PLoS One 9:e105710
Hardman, W Elaine (2014) Walnuts have potential for cancer prevention and treatment in mice. J Nutr 144:555S-560S
Hardman, W Elaine (2014) Diet components can suppress inflammation and reduce cancer risk. Nutr Res Pract 8:233-40
Abbas, Ata; Patterson 3rd, William; Georgel, Philippe T (2013) The epigenetic potentials of dietary polyphenols in prostate cancer management. Biochem Cell Biol 91:361-8
Fahrmann, Johannes F; Ballester, Oscar F; Ballester, Gabriela et al. (2013) Inhibition of nuclear factor kappa B activation in early-stage chronic lymphocytic leukemia by omega-3 fatty acids. Cancer Invest 31:24-38
Aimola, Pierpaolo; Carmignani, Marco; Volpe, Anna Rita et al. (2012) Cadmium induces p53-dependent apoptosis in human prostate epithelial cells. PLoS One 7:e33647
Nande, Rounak; Di Benedetto, Altomare; Aimola, Pierpaolo et al. (2012) Targeting a newly established spontaneous feline fibrosarcoma cell line by gene transfer. PLoS One 7:e37743

Showing the most recent 10 out of 47 publications