DNA methylation represents an important epigenetic mechanism that regulates a wide array of important biological processes. Abnormality in DNA methylation patterns is associated with various human disease conditions. In recent years, there has been a surge in research interest to address the potential modulating effect of various bioactive food components on DNA methylation, gene silencing, and reactivation. The overall objective of this application is aimed at providing systematic experimental evidence to establish a broad novel concept that many of the catecholic and noncatecholic polyphenols (e.g., tea catechins, bioflavonoids/isoflavonoids, coffee polyphenols) abundantly present in our daily diet constitute a major class of highly effective and consequential modulators of DNA methylation in vivo. This hypothesis is proposed on the basis of extensive preliminary data showing that dietary polyphenolic compounds can effectively modulate DNA methylation status in vitro and also in cultured cells. To achieve the goals, four broad-scoped but tightly-interlaced specific aims are planned to: 1) Determine in vitro inhibition of human DNMTs by various dietary polyphenols, and also study the kinetic mechanisms of human DNMT inhibition; 2) Conduct molecular modeling studies to determine the precise molecular mechanisms of human DNMT inhibition by active dietary polyphenols, and also to probe the structure-activity relationship of human DNMT inhibition by these dietary chemicals; 3) Study the effect of dietary polyphenols on DNA methylation and gene expression in human cancer cells grown in culture and in nude mice as xenografts;and 4) Study the effect of dietary polyphenols on DNA methylation, gene reactivation, and also on epigenetically-controlled phenotypes in mouse embryonic cells in culture and also in an intact animal model. It is expected that the outcomes of the proposed studies will have direct clinical utility in the near future and far-reaching human health implications.

Agency
National Institute of Health (NIH)
Institute
National Institute of Environmental Health Sciences (NIEHS)
Type
Research Project (R01)
Project #
5R01ES015242-05
Application #
7645082
Study Section
Special Emphasis Panel (ZES1-LWJ-E (EP))
Program Officer
Tyson, Frederick L
Project Start
2006-09-25
Project End
2012-06-30
Budget Start
2009-07-01
Budget End
2012-06-30
Support Year
5
Fiscal Year
2009
Total Cost
$349,706
Indirect Cost
Name
University of Kansas
Department
Pharmacology
Type
Schools of Medicine
DUNS #
016060860
City
Kansas City
State
KS
Country
United States
Zip Code
66160
Yamabe, Noriko; Kang, Ki Sung; Lee, Woojung et al. (2015) Estriol blunts postprandial blood glucose rise in male rats through regulating intestinal glucose transporters. Am J Physiol Endocrinol Metab 308:E370-9
Jiang, Xiang-Rong; Wang, Pan; Smith, Carolyn L et al. (2013) Synthesis of novel estrogen receptor antagonists using metal-catalyzed coupling reactions and characterization of their biological activity. J Med Chem 56:2779-90
Fukui, Masayuki; Kang, Ki Sung; Okada, Kazushi et al. (2013) EPA, an omega-3 fatty acid, induces apoptosis in human pancreatic cancer cells: role of ROS accumulation, caspase-8 activation, and autophagy induction. J Cell Biochem 114:192-203
Kang, Ki Sung; Yamabe, Noriko; Wen, Yujing et al. (2013) Beneficial effects of natural phenolics on levodopa methylation and oxidative neurodegeneration. Brain Res 1497:1-14
Fukui, Masayuki; Choi, Hye Joung; Zhu, Bao Ting (2012) Rapid generation of mitochondrial superoxide induces mitochondrion-dependent but caspase-independent cell death in hippocampal neuronal cells that morphologically resembles necroptosis. Toxicol Appl Pharmacol 262:156-66
Choi, Hye Joung; Fukui, Masayuki; Zhu, Bao Ting (2011) Role of cyclin B1/Cdc2 up-regulation in the development of mitotic prometaphase arrest in human breast cancer cells treated with nocodazole. PLoS One 6:e24312
Zhou, Ru; Lai, Yanlai; Yamabe, Noriko et al. (2011) Estriol has different effects from 17?-estradiol in modulating mouse splenocyte function under inflammatory conditions. J Immunotoxicol 8:346-58
Choi, Hye Joung; Kang, Ki Sung; Fukui, Masayuki et al. (2011) Critical role of the JNK-p53-GADD45ýý apoptotic cascade in mediating oxidative cytotoxicity in hippocampal neurons. Br J Pharmacol 162:175-92
Fukui, Masayuki; Zhu, Bao Ting (2010) Mitochondrial superoxide dismutase SOD2, but not cytosolic SOD1, plays a critical role in protection against glutamate-induced oxidative stress and cell death in HT22 neuronal cells. Free Radic Biol Med 48:821-30
Fu, Xin-Miao; Zhu, Bao Ting (2010) Human pancreas-specific protein disulfide-isomerase (PDIp) can function as a chaperone independently of its enzymatic activity by forming stable complexes with denatured substrate proteins. Biochem J 429:157-69

Showing the most recent 10 out of 27 publications