Identification of genes up-regulated by histone deacetylase inhibition with cDNA microarray and exploration of epigenetic alterations on hepatoma cells

被引:88
作者
Chiba, T
Yokosuka, O
Arai, M
Tada, M
Fukai, K
Imazeki, F
Kato, M
Seki, N
Saisho, H
机构
[1] Chiba Univ, Grad Sch Med, Dept Med & Clin Oncol, Chiba 2608670, Japan
[2] Chiba Univ, Grad Sch Med, Dept Funct Genom, Chiba 2608670, Japan
关键词
cDNA microarray; trichostatin A; HDAC inhibitor; histone acetylation; DNA methylation; hepatoma;
D O I
10.1016/j.jhep.2004.05.018
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background/Aims: Epigenetics is the key factor in the regulation of gene expression. We conducted cDNA microarray analysis to screen for genes induced by histone deacetylase (HDAC) inhibition and examined epigenetic alterations. Methods: Microarray analysis was performed in six hepatoma cell lines and primary hepatocytes treated with trichostatin A (TSA). mRNA expression of several genes was examined by reverse transcription-polymerase chain reaction in TSA-treated cells and hepatoma samples. Acetylated histones and methylation status in 5'CpG islands was assessed by chromatin immunoprecipitation (ChIP) assay and bisulfite genomic sequencing, respectively. Results: Fifty-seven genes showed greater than 2-fold change after TSA treatment in multiple cell lines. Among them, four genes including p21(WAF1) exhibited substantial induction (greater than 5-fold changes). Decreased mRNA levels of these genes in hepatoma tissues were observed in more than half of patients. ChIP assay, in general, demonstrated a good correlation between mRNA expression and histone acetylation, but only a limited correlation with the methylated DNA in the promoter region. Conclusions: We identified 57 up-regulated genes by TSA treatment in hepatoma cells and some of them appeared to be cancer-related genes in hepatomas. The alterations in acetylated histones are likely closely associated with gene expression. (C) 2004 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:436 / 445
页数:10
相关论文
共 48 条
[1]  
BAYLIN SB, 1991, CANCER CELL-MON REV, V3, P383
[2]   Methylation of histone H3 Lys 4 in coding regions of active genes [J].
Bernstein, BE ;
Humphrey, EL ;
Erlich, RL ;
Schneider, R ;
Bouman, P ;
Liu, JS ;
Kouzarides, T ;
Schreiber, SL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (13) :8695-8700
[3]   DNA methylation patterns and epigenetic memory [J].
Bird, A .
GENES & DEVELOPMENT, 2002, 16 (01) :6-21
[4]   ABNORMAL STRUCTURE AND EXPRESSION OF P53 GENE IN HUMAN HEPATOCELLULAR-CARCINOMA [J].
BRESSAC, B ;
GALVIN, KM ;
LIANG, TJ ;
ISSELBACHER, KJ ;
WANDS, JR ;
OZTURK, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (05) :1973-1977
[5]  
Chen JJ, 1996, MOL CELL BIOL, V16, P4673
[6]  
CHIBA T, 2004, IN PRESS ONCOLOGY
[7]   Synergistic effect of histone hyperacetylation and DNA demethylation in the reactivation of the FMR1 gene [J].
Chiurazzi, P ;
Pomponi, MG ;
Pietrobono, R ;
Bakker, CE ;
Neri, G ;
Oostra, BA .
HUMAN MOLECULAR GENETICS, 1999, 8 (12) :2317-2323
[8]   Aberrant CpG-island methylation has non-random and tumour-type-specific patterns [J].
Costello, JF ;
Frühwald, MC ;
Smiraglia, DJ ;
Rush, LJ ;
Robertson, GP ;
Gao, X ;
Wright, FA ;
Feramisco, JD ;
Peltomäki, P ;
Lang, JC ;
Schuller, DE ;
Yu, L ;
Bloomfield, CD ;
Caligiuri, MA ;
Yates, A ;
Nishikawa, R ;
Huang, HJS ;
Petrelli, NJ ;
Zhang, XL ;
O'Dorisio, MS ;
Held, WA ;
Cavenee, WK ;
Plass, C .
NATURE GENETICS, 2000, 24 (02) :132-138
[9]   Characterization of the transforming growth factor-β1-induced apoptotic transcriptome in FaO hepatoma cells [J].
Coyle, B ;
Freathy, C ;
Gant, TW ;
Roberts, RA ;
Cain, K .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (08) :5920-5928
[10]   CpG island hypermethylation and tumor suppressor genes: a booming present, a brighter future [J].
Esteller, M .
ONCOGENE, 2002, 21 (35) :5427-5440