首页> 美国卫生研究院文献>Gut >Hypermethylation of the promoter region of the E-cadherin gene (CDH1) in sporadic and ulcerative colitis associated colorectal cancer
【2h】

Hypermethylation of the promoter region of the E-cadherin gene (CDH1) in sporadic and ulcerative colitis associated colorectal cancer

机译:E-钙粘蛋白基因(CDH1)启动子区域的甲基化在散发性和溃疡性结肠炎相关的大肠癌中

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

BACKGROUND—Ulcerative colitis associated colorectal cancer (UCACRC) has several distinctive clinicopathological and genetic features which differ from sporadic colorectal cancer (SCRC). Hypermethylation of the E-cadherin gene (CDH1) has not been described previously in colorectal cancer.
AIMS—A panel of SCRC and UCACRC were investigated for mutations in CDH1, and for hypermethylation of the promoter region of CDH1.
SUBJECTS AND METHODS—DNA was available from 14 patients with UCACRC and from 14 with SCRC. All exons of CDH1 were amplified with the polymerase chain reaction (PCR) and screened using single strand conformational polymorphism and direct sequencing. Hypermethylation of the CDH1 promoter region was determined by methylation specific PCR following bisulphite modification, and compared with E-cadherin protein expression from a previous immunohistochemistry study.
RESULTS—Thirteen of 28 cancers (46%) were hypermethylated in the CDH1 promoter region—eight cancers (57%) in the UCACRC group and five cancers (36%) in the SCRC group (NS)—and this correlated with reduced E-cadherin expression (p<0.05). There was a trend for methylation to be associated with a more advanced stage of cancer although this did not reach statistical significance. There were no mutations in CDH1 in either group although there were several polymorphisms.
CONCLUSION—We have demonstrated hypermethylation of the promoter region in CDH1 in 46% of colorectal cancers studied. There was no difference between the UCACRC and SCRC groups. Just as there are specific differences in the genetic changes between UCACRC and SCRC, there is also likely to be a large degree of overlap among the genetic pathways of these cancers.


>Keywords: hypermethylation; promoter region; E-cadherin (CDH1); ulcerative colitis; colorectal cancer
机译:背景技术与溃疡性结肠炎相关的结肠直肠癌(UCACRC)具有一些与散发性结肠直肠癌(SCRC)不同的临床病理和遗传特征。 E-钙粘着蛋白基因(CDH1)的超甲基化以前在结直肠癌中没有描述。
AIMS—研究了SCRC和UCACRC小组的CDH1突变以及CDH1启动子区域的超甲基化。 />主题与方法-DNA可从14例UCACRC和14例SCRC患者中获得。 CDH1的所有外显子通过聚合酶链反应(PCR)进行扩增,并使用单链构象多态性和直接测序进行筛选。亚硫酸氢盐修饰后,通过甲基化特异性PCR确定CDH1启动子区域的超甲基化,并与先前免疫组织化学研究中的E-钙粘蛋白蛋白表达进行比较。
结果-28个癌症中有13个(46%)在CDH1启动子中被超甲基化UCACRC组中有8种癌症(​​57%),SCRC组(NS)中有5种癌症(36%),这与E-钙粘蛋白表达降低相关(p <0.05)。尽管没有达到统计学显着性,但甲基化趋势与癌症的更晚期有关。尽管存在多个多态性,但两组中CDH1均没有突变。
结论—我们已证明在研究的46%的结直肠癌中CDH1中启动子区域的高甲基化。 UCACRC和SCRC组之间没有差异。正如UCACRC和SCRC之间的遗传变化存在特定差异一样,这些癌症的遗传途径之间也可能存在很大程度的重叠。


> >关键字:高甲基化;启动子区E-钙粘蛋白(CDH1);溃疡性结肠炎;大肠癌

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号