Elevated cellular polyamine levels and increased activity of ornithine decarboxylase (ODC), the first enzyme in polyamine biosynthesis, are hallmarks of tumor development in epithelial tissues. Our long-term research goal is to understand the role of polyamines in the promotion and progression of epithelial cancers in order to develop novel prevention and treatment strategies. The specific objective of this application is to determine the effect of temporal and spatial manipulation of polyamine biosynthesis on keratinocyte growth control as well as skin tumor promotion and maintenance. Our central hypothesis is that cellular putrescine levels, rather than overall polyamine content, regulate keratinocyte proliferation, differentiation and transformation. To explore this hypothesis transgenic mouse models were produced that enable temporal and spatial control of antizyme (AZ) or S-adenosylmethionine decarboxylase (AdoMetDC) expression that is regulated by doxycycline (Dox). Interestingly, both AZ and AdoMetDC-expressing mice exhibit a thin fur phenotype. AZ is a negative regulator of cellular polyamine content that inhibits putrescine synthesis by ODC, stimulates ODC degradation and suppresses exogenous polyamine uptake into the cell. AdoMetDC provides the aminopropyl groups that are necessary for synthesis of the higher polyamines spermidine and spermine from the diamine putrescine. Therefore, AZ suppresses putrescine biosynthesis while AdoMetDC activity can deplete putrescine through enhanced utilization.
The first Aim i s to determine the effect of altered putrescine levels on keratinocyte proliferation and differentiation during normal development and oncogene activation. First, skin sections will be analyzed to identify the developmental defects in hair follicle morphogenesis and cycling that are induced by AZ and AdoMetDC expression. Next, primary keratinocytes from our transgenic models will be utilized to measure proliferation, migration, and markers of differentiation and senescence in response to calcium or TPA- induced differentiation as well as activated HRAS expression in order to identify the molecular targets of putrescine regulation.
The second Aim i s to evaluate the ability of AZ and AdoMetDC to inhibit promotion of initiated cells and determine the cell-type and stage specificity of the tumor suppressive effects. First, chemical carcinogenesis will be utilized to demonstrate the ability of AZ and AdoMetDC to impair tumor promotion in mouse skin. Thereafter, transgene expression will be silenced to determine whether latent initiated cells persist in the skin of thes animals. Next, AZ expression will be targeted to suprabasal keratinocytes to determine if this cell type provides the putrescine that is required for promotion of initiated basal cells. Finally, expression will be induced in transgene-naive tumor-bearing animals to quantify the ability of AZ or AdoMetDC to induce regression or slow the growth of established tumors. The successful completion of these studies will lead to a more complete understanding of polyamine function in epithelial carcinogenesis and will enhance future development of polyamine-targeted therapies to prevent and treat cancer.

Public Health Relevance

This research project will utilize conditional transgenic mouse models to manipulate skin polyamine metabolism in specific cellular locations. We will elucidate the regulatory functions exerted by polyamines, especially putrescine, on keratinocyte growth control as well as tumor promotion and maintenance in the two- stage chemical carcinogenesis protocol. These studies are essential to the continued development of preventive and therapeutic agents to target polyamine metabolism in cancer.

Agency
National Institute of Health (NIH)
Type
Research Project (R01)
Project #
7R01CA018138-37
Application #
8827072
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Spalholz, Barbara A
Project Start
Project End
Budget Start
Budget End
Support Year
37
Fiscal Year
2014
Total Cost
Indirect Cost
Name
University of Virginia
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
City
Charlottesville
State
VA
Country
United States
Zip Code
22904
Nowotarski, Shannon L; Feith, David J; Shantz, Lisa M (2015) Skin Carcinogenesis Studies Using Mouse Models with Altered Polyamines. Cancer Growth Metastasis 8:17-27
Lange, Ingo; Geerts, Dirk; Feith, David J et al. (2014) Novel interaction of ornithine decarboxylase with sepiapterin reductase regulates neuroblastoma cell proliferation. J Mol Biol 426:332-46
Koomoa, Dana-Lynn T; Geerts, Dirk; Lange, Ingo et al. (2013) DFMO/eflornithine inhibits migration and invasion downstream of MYCN and involves p27Kip1 activity in neuroblastoma. Int J Oncol 42:1219-28
Feith, David J; Pegg, Anthony E; Fong, Louise Y Y (2013) Targeted expression of ornithine decarboxylase antizyme prevents upper aerodigestive tract carcinogenesis in p53-deficient mice. Carcinogenesis 34:570-6
Giordano, Emanuele; Hillary, Rebecca A; Vary, Thomas C et al. (2012) Overexpression of ornithine decarboxylase decreases ventricular systolic function during induction of cardiac hypertrophy. Amino Acids 42:507-18
Welsh, Patricia A; Sass-Kuhn, Suzanne; Prakashagowda, Chethana et al. (2012) Spermine synthase overexpression in vivo does not increase susceptibility to DMBA/TPA skin carcinogenesis or Min-Apc intestinal tumorigenesis. Cancer Biol Ther 13:358-68
Shi, Chenxu; Welsh, Patricia A; Sass-Kuhn, Suzanne et al. (2012) Characterization of transgenic mice with overexpression of spermidine synthase. Amino Acids 42:495-505
Shi, Chenxu; Cooper, Timothy K; McCloskey, Diane E et al. (2012) S-adenosylmethionine decarboxylase overexpression inhibits mouse skin tumor promotion. Carcinogenesis 33:1310-8
Green, Robert; Hanfrey, Colin C; Elliott, Katherine A et al. (2011) Independent evolutionary origins of functional polyamine biosynthetic enzyme fusions catalysing de novo diamine to triamine formation. Mol Microbiol 81:1109-24
Pegg, Anthony E (2011) Multifaceted roles of alkyltransferase and related proteins in DNA repair, DNA damage, resistance to chemotherapy, and research tools. Chem Res Toxicol 24:618-39

Showing the most recent 10 out of 111 publications