The equilibrative nucleoside transporters are integral membrane proteins that are essential for the uptake of nucleosides and chemotherapeutic nucleoside analogs (e.g. Ara-C, gemcitabine). Enhanced sensitivity to nucleoside analogs has been observed after combined chemotherapy (i.e. cisplatinum, irradiation), although the mechanism(s) responsible for these effects are poorly understood. The equilibrative nucleoside transporters (ENT1/2) are ubiquitously expressed and are differentially regulated depending on the exposure of cells to mitogens or stress signals. At present, the molecular events that control the transcriptional regulation of these transporters are unknown. Our lab has been investigating the regulation of pyrimidine nucleotide synthesis by protein kinases. Our recent studies have focused on the requirement of ENT 1/2 in the uptake of nucleoside and the salvage synthesis of pyrimidine nucleotides. Specifically our studies have pointed to a crucial role for Src and the stress-activated c-Jun kinases (JNK) in the regulation of ENT1/2 expression. Thus the objective of this proposal is to characterize the kinase-dependent signals that are necessary for the transcriptional regulation of ENT 1/2, and to determine the impact of this event on cell proliferation or survival. In addition, we will determine the promoter elements that are required for kinase-mediated regulation of ENT1/2 expression. Finally, we will investigate whether activation of JNK is involved in the up-regulation and enhanced sensitization of cells to nucleoside analogs.
The Specific Aims of the proposal are:
Aim #1. Determine the involvement of specific protein kinases in the regulation of ENT1/2 expression.
Aim #2. Elucidate the promoter elements necessary for the expression of ENT1 and ENT2.
Aim #3. Examine the specific roles of ENTs in growth, differentiation and chemosensitization .

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM069976-03
Application #
7100888
Study Section
Xenobiotic and Nutrient Disposition and Action Study Section (XNDA)
Program Officer
Okita, Richard T
Project Start
2004-08-01
Project End
2008-07-31
Budget Start
2006-08-01
Budget End
2007-07-31
Support Year
3
Fiscal Year
2006
Total Cost
$284,108
Indirect Cost
Name
University of North Carolina Chapel Hill
Department
Pharmacology
Type
Schools of Medicine
DUNS #
608195277
City
Chapel Hill
State
NC
Country
United States
Zip Code
27599
Leisewitz, Andrea V; Zimmerman, Eric I; Huang, Min et al. (2011) Regulation of ENT1 expression and ENT1-dependent nucleoside transport by c-Jun N-terminal kinase. Biochem Biophys Res Commun 404:370-5
Kassel, Karen M; Au, Da Ryung; Higgins, Matthew J et al. (2010) Regulation of human cytidine triphosphate synthetase 2 by phosphorylation. J Biol Chem 285:33727-36
Wang, Qunzhao; Zimmerman, Eric I; Toutchkine, Alexei et al. (2010) Multicolor monitoring of dysregulated protein kinases in chronic myelogenous leukemia. ACS Chem Biol 5:887-95
Zimmerman, Eric I; Huang, Min; Leisewitz, Andrea V et al. (2009) Identification of a novel point mutation in ENT1 that confers resistance to Ara-C in human T cell leukemia CCRF-CEM cells. FEBS Lett 583:425-9
Huang, Min; Wang, Yanhong; Gu, Jingjin et al. (2008) Determinants of sensitivity of human T-cell leukemia CCRF-CEM cells to immucillin-H. Leuk Res 32:1268-78
Leisewitz, Andrea V; Zimmerman, Eric I; Jones, Shannon Z et al. (2008) Imatinib-resistant CML cells have low ENT activity but maintain sensitivity to gemcitabine. Nucleosides Nucleotides Nucleic Acids 27:779-86
Higgins, M J; Loiselle, D; Haystead, T A et al. (2008) Human cytidine triphosphate synthetase 1 interacting proteins. Nucleosides Nucleotides Nucleic Acids 27:850-7
Koseoglu, M Murat; Graves, Lee M; Marzluff, William F (2008) Phosphorylation of threonine 61 by cyclin a/Cdk1 triggers degradation of stem-loop binding protein at the end of S phase. Mol Cell Biol 28:4469-79