Downregulation of CD44v6 in colorectal carcinomas is associated with hypermethylation of the CD44 promoter region

被引:11
|
作者
Stallmach, A [1 ]
Wittig, BM
Kremp, K
Goebel, R
Santourlidis, S
Zeitz, M
Menges, M
Raedle, J
Zeuzem, S
Schulz, WA
机构
[1] Univ Saarland, Dept Internal Med 2, D-66421 Homburg, Germany
[2] Univ Dusseldorf, Dept Urol, D-040225 Dusseldorf, Germany
[3] Free Univ Berlin, Klinikum Benjamin Franklin, Med Clin 1, D-12200 Berlin, Germany
关键词
CD44; variants; colorectal carcinoma; methylation; promoter;
D O I
10.1016/S0014-4800(03)00025-X
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Overexpression of the cell adhesion protein CD44v6 has been demonstrated in colorectal cancer and other gastrointestinal tumors. While CD44v6 is upregulated in benign colorectal adenomas and well-differentiated colorectal cancer tissues, downregulation frequently occurs during disease progression. The mechanism of downregulation, however, is unknown. Therefore, we evaluated the methylation status of the CD44 promoter as a mechanism for decreased CD44v6 expression in advanced colorectal carcinomas. We demonstrated by methylation-sensitive restriction enzyme digestion that the CpG islands of the CD44 promoter were methylated in 6/21 (28%) of benign colorectal adenomas. Interestingly, in colorectal carcinomas the frequency of promoter methylation was significantly increased (10/19; 53%) compared to 7/21 (33%) in the corresponding normal mucosa. Methylation seems to be associated with a more advanced cancer stage, but the trend did not reach statistical significance. In colorectal carcinomas with CD44 promoter methylation CD44v6 mRNA was detected by reverse transcription-polymerase chain reaction in 3/10 carcinomas, whereas in tumors without CD44 promoter methylation CD44v6 expression was observed in 8/9 (P less than or equal to 0.05). These results demonstrated that methylation of the 5'CpG island of the CD44 gene is closely associated with decreased expression of CD44v6 in human colorectal carcinomas. (C) 2003 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:262 / 266
页数:5
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