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An overview of epigenetics and chemoprevention
Authors:Huang Yi-Wen  Kuo Chieh-Ti  Stoner Kristen  Huang Tim H-Y  Wang Li-Shu
Affiliation:aHuman Cancer Genetics Program, Comprehensive Cancer Center, The Ohio State University, Columbus, OH 43210, United States;bComprehensive Cancer Center, College of Medicine, The Ohio State University, Columbus, OH 43210, United States
Abstract:It is now appreciated that both genetic alteration, e.g. mutations, and aberrant epigenetic changes, e.g. DNA methylation, cause cancer. Epigenetic dysregulation is potentially reversible which makes it attractive as targets for cancer prevention. Synthetic drugs targeting enzymes, e.g. DNA methyltransferase and histone deacetylase, that regulate epigenetic patterns are active in clinical settings. In addition, dietary factors have been suggested to have potential to reverse aberrant epigenetic patterns. Uncovering the human epigenome can lead us to better understand the dynamics of DNA methylation in disease progression which can further assist in cancer prevention.
Keywords:Abbreviations: DNMT, DNA methyltransferase   SAM, S-adenosylmethionine   HAT, histone acetylase   HDAC, histone deacetylase   MBD, methyl-CpG-binding domain   IBD, inflammatory bowel disease   SFRP, secreted frizzled-related protein   APC, adenomatous polyposis coli   ACF, aberrant crypt foci   DES, diethylstilbestrol   S1P, sphingosine-1-phosphate   SphK2, sphingosine kinase 2   SAHA, suberoylanilide hydroxamic acid   TSA, trichostatin   BRBs, freeze-dried black raspberries   WIF, Wnt inhibitory factor   EGCG, (&minus  )-epigallocatechin 3-gallate   RAR, retinoic acid receptor   NSCLC, non-small-cell lung cancer   CDH13, cadherin 13   RASSF1A, ras association domain family protein 1A   PITX2, pituitary homeobox 2   COMT, catechol-o-methyltransferase   CYP, cytochrome P450   NAT1, N-acetyltransferase type 1   SULT1A1, sulfotransferase 1A1   CIMP, CpG island methylator phenotype   BMP-4, bone morphogenetic protein-4   FGF4, fibroblast growth factor 4   CDO1, cysteine dioxygenase 1   MGMT, O-6-methylguanine-DNA methyltransferase   5-FU, 5-fluorouracil
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