The transcription factor NF-E2 and the gene encoding PRV-1 are overexpressed in patients with? polycythemia vera (PV). The recent description of a Jak2V617F mutation in PV patients raises the question? whether this allele exerts its effect on the malignant clone in part through inducing NF-E2 expression. NF-E2? is a promising candidate in the pathophysiology of PV for several reasons:? NF-E2 is overexpressed in stem cells as well as in all three cell lineages affected in PV. In murine cells NFE2? overexpression leads to Epo-independent growth and differentiation. NF-E2 may thus play a pivotal role? in causing the erythrocytosis of PV. However, both the molecular mechanism leading to NF-E2? overexpression and its effect on human hematopoiesis are not known. In addition, the cause of PRV-1? overexpression remains unclear. Therefore, it is the aim of this project to investigate the cause of NF-E2? and PRV-1 overexpression in PV and the effect of NF-E2 overexpression in hematopoietic cells.? Based on the following hypotheses, the specific aims of this project are therefore:? 1. Hypothesis: NF-E2 is required for the Epo-independent growth of PV cells or its overexpression? modulates hematopoietic differentiation.
Specific Aim : To modulate NF-E2 expression via siRNA knock down? and retroviral or lentiviral transduction and examine the consequences on Epo-dependent and -independent? growth in vitro.? 2. Hypothesis: NF-E2 and PRV-1 overexpression in PV are mediated by the Jak2V617F allele Specific Aim:? To introduce Jak2 wt and V617F alleles in vivo and in vitro and examine the effects on NF-E2 and PRV-1? expression in various models.? 3. Hypothesis: NF-E2 and PRV-1 overexpression result from aberrant transcriptional activation Specific Aim:? To characterize protein/DNA interaction on the NF-E2 and PRV-1 promoters in PV and healthy control cells? to determine aberrantly activated transcription factors.? Public Health Implications: By leading to a better understanding of the molecular changes that lead to the? development of PV, this project will point out molecules against which new drugs for treatment can be? developed.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Program Projects (P01)
Project #
5P01CA108671-03
Application #
7691286
Study Section
Subcommittee G - Education (NCI)
Project Start
Project End
Budget Start
2008-07-01
Budget End
2009-06-30
Support Year
3
Fiscal Year
2008
Total Cost
$339,359
Indirect Cost
Name
Icahn School of Medicine at Mount Sinai
Department
Type
DUNS #
078861598
City
New York
State
NY
Country
United States
Zip Code
10029
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