The goal of this research is to reveal the molecular mechanism(s) by which alterations in base excision repair (BER) activity affect cancer susceptibility. The objective of this research is to elucidate the mechanism by which folate deficiency results in a phenotype of DNA repair deficiency. Because DNA repair deficiency increases susceptibility to cancer, it is reasonable to suggest that identification of the underlying mechanisms by which folate deficiency inhibits DNA repair will be informative with respect to the underlying mechanisms by which folate deficiency increases cancer risk. My hypothesis is that folate deficiency reduces tolerance to DNA damage and induces a functional BER deficiency by altering the regulation of (- pol.
Specific Aim 1 : Establish that a lack of dietary folate results in a functional BER deficiency.
Specific Aim 2 : Establish that a lack of dietary folate prevents upregulation of (-pol in response to carcinogen exposure, blocking the BER response to oxidative damage.
Specific Aim 3 : Establish the mechanism by which a lack of dietary folate alters regulation of (-pol. The loss of the BER response to DNA damage when folate is deficient would establish a mechanism by which diet can alter susceptibility to environmental exposure. ? ? ?

Agency
National Institute of Health (NIH)
Institute
National Institute of Environmental Health Sciences (NIEHS)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
5F32ES013643-02
Application #
6951231
Study Section
Special Emphasis Panel (ZRG1-F09 (20))
Program Officer
Humble, Michael C
Project Start
2004-09-30
Project End
2007-09-29
Budget Start
2005-09-30
Budget End
2006-09-29
Support Year
2
Fiscal Year
2005
Total Cost
$49,928
Indirect Cost
Name
Wayne State University
Department
Pharmacology
Type
Schools of Medicine
DUNS #
001962224
City
Detroit
State
MI
Country
United States
Zip Code
48202
Simon, Kirk; Mukundan, Anju; Dewundara, Samantha et al. (2009) Transcriptional profiling of the age-related response to genotoxic stress points to differential DNA damage response with age. Mech Ageing Dev 130:637-47
Kanellis, Pamela; Gagliardi, Mark; Banath, Judit P et al. (2007) A screen for suppressors of gross chromosomal rearrangements identifies a conserved role for PLP in preventing DNA lesions. PLoS Genet 3:e134
Cabelof, Diane C; Raffoul, Julian J; Ge, Yubin et al. (2006) Age-related loss of the DNA repair response following exposure to oxidative stress. J Gerontol A Biol Sci Med Sci 61:427-34
Cabelof, Diane C; Ikeno, Yuji; Nyska, Abraham et al. (2006) Haploinsufficiency in DNA polymerase beta increases cancer risk with age and alters mortality rate. Cancer Res 66:7460-5
Cabelof, Diane C; Nakamura, Jun; Heydari, Ahmad R (2006) A sensitive biochemical assay for the detection of uracil. Environ Mol Mutagen 47:31-7