CpG island methylation in aberrant crypt foci and cancers from the same patients

被引:34
|
作者
Luo, LP
Chen, WD
Pretlow, TP
机构
[1] Case Western Reserve Univ, Inst Pathol, Cleveland, OH 44106 USA
[2] Case Western Reserve Univ, Case Comprehens Canc Ctr, Cleveland, OH 44106 USA
[3] Case Western Reserve Univ, Dept Med, Cleveland, OH 44106 USA
关键词
premalignant lesion; epigenetic alteration; hypermethylation; colon cancer;
D O I
10.1002/ijc.20936
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Aberrant methylation of CpG islands is a common alteration in human colon cancer. Methylation of only a limited number of loci has been studied in aberrant crypt foci (ACF), the earliest identified premalignant lesions in the colon, and in only a limited number of lesions from the same patients. Methylation-specific PCR was used to analyze 35 ACF, samples of normal crypts with the same number of crypts as were in each ACF and 22 cancers from the same patients. Aberrant methylation in cellular retinol-binding protein 1 (CRBP1), MINT31 or H-cadherin (CDH13) was identified in 19 of 35 (54%) ACF. Hypermethylation of CRBP1, MINT31 or CDH13 was more frequent (15 of 22, 68%) in cancers. DNA methylation of CRBP1, MINT31 or CDH13 was not correlated between cancers and ACF from the same patients. Aberrant methylation was not correlated with patient age, number of crypts in the ACF or cancer stage. These results suggest that hypermethylation in the promoter region of some genes is an independent event, occurs early in human colon tumorigenesis and may play an important role during the transformation and progression of some lesions to colon cancers. (c) 2005 Wiley-Liss, Inc.
引用
收藏
页码:747 / 751
页数:5
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