More than 1 million cases of nonmelanoma skin cancer and 59,600 cases of melanoma are diagnosed yearly in the United States, resulting in about 10,600 deaths (about 7,800 due to melanoma) in 2005. In recent years it has become clear that UV-damaged skin has an increased chance of developing one of the forms of skin cancer, including basal cell carcinoma, squamous cell carcinoma and cutaneous malignant melanoma. The apoptotic response to UV is a protective response that eliminates cells that receive high doses of UV. While most studies have focused on DNA damage-inducible, p53-dependent pathways of UV-induced apoptosis, membrane receptor mediated signaling pathways also play an important role in inducing apoptosis. UV-irradiation activates kinases that phosphorylate the alpha subunit of eukaryotic initiation factor 2 (eIF21) and subsequently inhibit protein synthesis. Translation plays an important role in regulation of apoptotic gene expression. However, the upstream signaling pathway(s) that leads to eIF21 kinase(s) activation upon UV-irradiation is not known. The objective of this application is to elucidate the mechanisms that regulate UV-induced apoptosis via nitric oxide synthase (NOS) mediated signaling pathways and to determine the roles of nitric oxide (NO)/peroxynitrite (ONOO) and zinc (Zn2+) in UV-induced translation regulation and apoptosis. The research proposed in this application is significant because understanding the regulation of NOS activation and how this regulation affects eIF21 kinase(s) activation and/or apoptosis upon UV-irradiation will lead us to a new signaling network for identification of target genes and development of therapeutics in the prevention and treatment of UV-related cancers.
In Specific Aim I, we proposed to elucidate the UV-induced and NO-mediated signaling pathway(s) that leads to eIF21 phosphorylation. The working hypothesis is that NO mediates UV-induced activations of eIF21 kinase(s), which phosphorylate eIF21.
In Specific Aim II : we proposed to determine the mechanism and kinetics of NO/ONOO/ production and their role in UV-induced apoptosis. The working hypothesis is that at a high ratio of NO:ONOO, the effect of UV can be anti-apoptotic, while at a low ratio this effect can be pro-apoptotic.
In Specific Aim III, we proposed to determine the role(s) of Zn in UV-induced ER-stress and apoptotic signaling pathways. The working hypothesis is that [Zn2+] mediates NO-induced apoptosis upon UV- irradiation. The outcomes from this research will not only increase our knowledge of UV- induced and NOS-mediated multiple signaling pathways, but will also lead to a further understanding of regulatory mechanisms and signaling pathways induced by other physiological conditions (e.g., reperfusion, wound healing, diabetes) that are affected by NO and translation inhibition.

Public Health Relevance

Cell death induced by ultraviolet light (UV) is a protective response that eliminates damaged cells. In the proposal, we will study the mechanisms that regulate UV-induced apoptosis via nitric oxide synthase mediated signaling pathways and to determine the roles of nitric oxide/peroxynitrite and cytosolic zinc concentration in UV-induced translation regulation and apoptosis. The outcomes from these studies will not only increase our knowledge of UV- induced multiple apoptotic signaling pathways, but will also lead us to the development of new therapeutics for treatment of UV-related skin aging and cancers.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
5R01CA086928-10
Application #
8298670
Study Section
Radiation Therapeutics and Biology Study Section (RTB)
Program Officer
Okano, Paul
Project Start
2000-09-01
Project End
2013-07-31
Budget Start
2012-08-01
Budget End
2013-07-31
Support Year
10
Fiscal Year
2012
Total Cost
$254,434
Indirect Cost
$81,936
Name
Ohio University Athens
Department
Chemistry
Type
Schools of Arts and Sciences
DUNS #
041077983
City
Athens
State
OH
Country
United States
Zip Code
45701
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