): The purpose of this program is to train a new generation of researchers and educators in signal transduction mechanisms. Signal transduction is the means by which cells respond to internal and external stimuli. These controls regulate the physiology, metabolism and gene control of the cell. As such, the signal transduction is fundamental to all cells and is critical to the understanding of many pathologic states. In this program the applicants focus on training related to cancer; cancer has been termed a disease of aberrant signaling mechanisms. The program, however, is not limited to problems in cancer and involves many clinical problems and departments. Here the applicants propose that the training program faculty from the Departments of Medicine, Biochemistry, Physiology/Pharmacology and Microbiology/Immunology will be responsible for the didactic and research training of seven fellows. Four of these fellows will be predoctoral and three will be postdoctoral. The postdoctorals can have either the M.D. or Ph.D. degree. The program will be 4-5 years for predoctoral and 2-3 years for postdoctoral fellows. The facilities of the Departments involved plus those of the Comprehensive Cancer Center of Wake Forest University will be available to the trainees.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Institutional National Research Service Award (T32)
Project #
5T32CA009422-17
Application #
2748680
Study Section
Subcommittee G - Education (NCI)
Program Officer
Eckstein, David J
Project Start
1986-09-01
Project End
2002-05-31
Budget Start
1998-08-01
Budget End
1999-07-31
Support Year
17
Fiscal Year
1998
Total Cost
Indirect Cost
Name
Wake Forest University Health Sciences
Department
Biochemistry
Type
Schools of Medicine
DUNS #
937727907
City
Winston-Salem
State
NC
Country
United States
Zip Code
27157
Connor, John H; Lyles, Douglas S (2005) Inhibition of host and viral translation during vesicular stomatitis virus infection. eIF2 is responsible for the inhibition of viral but not host translation. J Biol Chem 280:13512-9
Shen, You-Jun; DeLong, Cynthia J; Terce, Francois et al. (2005) Polyploid formation via chromosome duplication induced by CTP:phosphocholine cytidylyltransferase deficiency and Bcl-2 overexpression: identification of two novel endogenous factors. J Histochem Cytochem 53:725-33
Grab, Leslie T; Kearns, Mary W; Morris, Andrew J et al. (2004) Differential role for phospholipase D1 and phospholipase D2 in 12-O-tetradecanoyl-13-phorbol acetate-stimulated MAPK activation, Cox-2 and IL-8 expression. Biochim Biophys Acta 1636:29-39
Connor, John H; Naczki, Christine; Koumenis, Costas et al. (2004) Replication and cytopathic effect of oncolytic vesicular stomatitis virus in hypoxic tumor cells in vitro and in vivo. J Virol 78:8960-70
Cui, Zheng; Willingham, Mark C; Hicks, Amy M et al. (2003) Spontaneous regression of advanced cancer: identification of a unique genetically determined, age-dependent trait in mice. Proc Natl Acad Sci U S A 100:6682-7
Connor, John H; Lyles, Douglas S (2002) Vesicular stomatitis virus infection alters the eIF4F translation initiation complex and causes dephosphorylation of the eIF4E binding protein 4E-BP1. J Virol 76:10177-87
Tran, Khai; Thorne-Tjomsland, Gro; DeLong, Cynthia J et al. (2002) Intracellular assembly of very low density lipoproteins containing apolipoprotein B100 in rat hepatoma McA-RH7777 cells. J Biol Chem 277:31187-200
Baker, Paul R S; Owen, John S; Nixon, Andrew B et al. (2002) Regulation of platelet-activating factor synthesis in human neutrophils by MAP kinases. Biochim Biophys Acta 1592:175-84
DeLong, Cynthia J; Hicks, Amy M; Cui, Zheng (2002) Disruption of choline methyl group donation for phosphatidylethanolamine methylation in hepatocarcinoma cells. J Biol Chem 277:17217-25
Moors, M A; Li, L; Mizel, S B (2001) Activation of interleukin-1 receptor-associated kinase by gram-negative flagellin. Infect Immun 69:4424-9

Showing the most recent 10 out of 61 publications