Regulation of hMSH2 and hMLH1 expression in the human colon cancer cell line SW1116 by DNA methyltransferase 1

被引:24
作者
Fang, JY
Lu, R
Mikovits, JA
Cheng, ZH
Zhu, HY
Chen, YX
机构
[1] Shanghai Med Univ 2, Renji Hosp, Shanghai Inst Digest Dis, Shanghai 200001, Peoples R China
[2] Pacific Technol Ctr, EpiGenX Pharmaceut, Santa Barbara, CA 93111 USA
关键词
DNA methyltransferase 1; transfection; mismatch repair gene; colon cancer cell line; expression; antisense construct;
D O I
10.1016/j.canlet.2005.03.005
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Aberrant DNA methylation is now recognized as an important epigenetic alteration occurring early in human cancer. To directly study the role of DNA methltransferase 1 (DNMT1) in the regulation of expression of tumor-related genes in human colon cancer cells, we stably transfected expression constructs containing sense or antisense DNMT1 into the human colon cancer cell line, SW1116. The expression level of mismatch repair genes (MMR), human mut-L homologue 1 (hMLH1) and human Mut S homologue 2 (hMSH2), was monitored by real-time RT-PCR. The methylation status of hMLH1 and hMSH2 promoters was determined by bisulfite modification and methylation-specific PCR (MSP). The protein levels of DNMT1 hMSH2 and hMLH1 were determined by Western analysis. The results show that DNMT1 protein expression was increased or decreased in transfected cell lines containing sense or antisense DNMT1 constructs, respectively. In cells expressing the sense DNMT1 construct, the expression of hMLH1 and hMSH2 was down-regulated through hypermethylation of their respective promoters. Furthermore, antisense DNMT1 expression induced promoter demethylation and up-regulated transcription of hMSH2 (P < 0.05) and hMLH1 (P=0.064) in SW 1116 cells. (c) 2005 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:124 / 130
页数:7
相关论文
共 29 条
[1]  
ALTHAUS F, 2005, ONCOGENE, P2411
[2]   NUMBER OF CPG ISLANDS AND GENES IN HUMAN AND MOUSE [J].
ANTEQUERA, F ;
BIRD, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (24) :11995-11999
[3]   Tying it all together: Epigenetics, genetics, cell cycle, and cancer [J].
Baylin, SB .
SCIENCE, 1997, 277 (5334) :1948-1949
[4]   Gene silencing - a new theory of aging [J].
Burzynski, SR .
MEDICAL HYPOTHESES, 2003, 60 (04) :578-583
[5]  
CHEN X, 2000, CHIN MED J, V115, P1048
[6]  
CLARK SJ, 1994, NUCLEIC ACIDS RES, V22, P2990, DOI 10.1093/nar/22.15.2990
[7]  
Cote S, 1998, ANTI-CANCER DRUG, V9, P743
[8]  
Esteller M, 2000, CANCER RES, V60, P4366
[9]   Infection of lymphoid cells by integration-defective human immunodeficiency virus type 1 increases de novo methylation [J].
Fang, JY ;
Mikovits, JA ;
Bagni, R ;
Petrow-Sadowski, CL ;
Ruscetti, FW .
JOURNAL OF VIROLOGY, 2001, 75 (20) :9753-9761
[10]   Effects of DNA methylation on expression of tumor suppressor genes and proto-oncogene in human colon cancer cell lines [J].
Fang, JY ;
Lu, J ;
Chen, YX ;
Yang, L .
WORLD JOURNAL OF GASTROENTEROLOGY, 2003, 9 (09) :1976-1980