Excavating relics of DNA methylation changes during the development of neoplasia

被引:19
作者
Hsiao, Shu-Huei [1 ,2 ]
Huang, Tim H-M. [3 ]
Leu, Yu-Wei [1 ,2 ]
机构
[1] Natl Chung Cheng Univ, Human Epigenom Ctr, Dept Life Sci, Chiayi 621, Taiwan
[2] Natl Chung Cheng Univ, Inst Mol Biol, Chiayi 621, Taiwan
[3] Ohio State Univ, Human Canc Genet Program, Dept Mol Virol Immunol & Med Genet, Ctr Comprehens Canc, Columbus, OH 43210 USA
关键词
Epigenetics; DNA methylation; Cancer and cell signaling; CPG ISLAND METHYLATION; DEPENDENT KINASE INHIBITOR; TUMOR-SUPPRESSOR GENES; STEM-CELL BIOLOGY; HUMAN-MALIGNANT MELANOMA; COLORECTAL-CANCER; HISTONE H3; EPIGENETIC REGULATION; RETT-SYNDROME; HEPATOCELLULAR-CARCINOMA;
D O I
10.1016/j.semcancer.2009.02.015
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Epigenetic events like DNA methylation are known to regulate gene expression, and dysregulation of these events is associated with neoplastic proliferation. Here, we provide a step-by-step review of the approach that has gradually developed to identify critical DNA methylation during neoplasia. DNA methylation has first been tightly linked to the regulation of gene expression and functions. Next, the clinical importance of such DNA methylation has been probed by inducing loss of the maintenance of normal DNA methylation, which has been found to trigger onset of disease. Methylation changes can be signal-specific and lineage-specific, providing a record what cells have encountered and what they have become. Comparison of methylation associated with normal cellular differentiation and abnormal cell fate changes is expected to uncover critical methylation changes. We also propose a specific scheme that can be used to excavate critical DNA methylation associated with cell evolution. (C) 2009 Published by Elsevier Ltd.
引用
收藏
页码:198 / 208
页数:11
相关论文
共 164 条
[1]   UTX and JMJD3 are histone H3K27 demethylases involved in HOX gene regulation and development [J].
Agger, Karl ;
Cloos, Paul A. C. ;
Christensen, Jesper ;
Pasini, Diego ;
Rose, Simon ;
Rappsilber, Juri ;
Issaeva, Irina ;
Canaani, Eli ;
Salcini, Anna Elisabetta ;
Helin, Kristian .
NATURE, 2007, 449 (7163) :731-U10
[2]  
Akkiprik M, 2007, J GASTROINTEST LIVER, V16, P11
[4]   Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2 [J].
Amir, RE ;
Van den Veyver, IB ;
Wan, M ;
Tran, CQ ;
Francke, U ;
Zoghbi, HY .
NATURE GENETICS, 1999, 23 (02) :185-188
[5]  
[Anonymous], DEV BIOL BASEL
[7]   Epigenetic regulation of CD133 and tumorigenicity of CD133+ovarian cancer cells [J].
Baba, T. ;
Convery, P. A. ;
Matsumura, N. ;
Whitaker, R. S. ;
Kondoh, E. ;
Perry, T. ;
Huang, Z. ;
Bentley, R. C. ;
Mori, S. ;
Fujii, S. ;
Marks, J. R. ;
Berchuck, A. ;
Murphy, S. K. .
ONCOGENE, 2009, 28 (02) :209-218
[8]   Epigenetic "bivalently marked" process of cancer stem cell-driven tumorigenesis [J].
Balch, Curt ;
Nephew, Kenneth P. ;
Huang, Tim H. -M. ;
Bapat, Sharmila A. .
BIOESSAYS, 2007, 29 (09) :842-845
[9]   The impact of MECP2 mutations in the expression patterns of Rett syndrome patients [J].
Ballestar, E ;
Ropero, S ;
Alaminos, M ;
Armstrong, J ;
Setien, F ;
Agrelo, R ;
Fraga, MF ;
Herranz, M ;
Avila, S ;
Pineda, M ;
Monros, E ;
Esteller, M .
HUMAN GENETICS, 2005, 116 (1-2) :91-104
[10]   Epigenetic Gene Regulation in Cancer [J].
Ballestar, Esteban ;
Esteller, Manel .
LONG-RANGE CONTROL OF GENE EXPRESSION, 2008, 61 :247-267