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CDX1在结直肠癌中的表达降低,且与启动子高甲基化有关。

CDX1 expression is reduced in colorectal carcinoma and is associated with promoter hypermethylation.

作者信息

Pilozzi Emanuela, Onelli Mariadele Rapazzotti, Ziparo Vincenzo, Mercantini Paolo, Ruco Luigi

机构信息

Department of Laboratory Medicine and Pathology, Sant'Andrea Hospital, University La Sapienza, Rome, Italy.

出版信息

J Pathol. 2004 Nov;204(3):289-95. doi: 10.1002/path.1641.

Abstract

The CDX1 homeobox gene encodes a transcription factor specifically expressed in normal intestinal and colonic epithelia, and CDX1 gene expression is affected during colorectal tumour progression. In this study, real-time quantitative RT-PCR was used to investigate CDX1 expression in 26 colorectal carcinomas. Reduced expression of CDX1 was observed in 19 of 26 colon carcinomas compared to matched normal colonic mucosa: the decrease in CDX1 expression ranged between 0.10 and 0.79 (21-90% decrease; mean 64.75% +/-22; p = 0.001). Mutation and loss of heterozygosity (LOH) analyses were then used to determine if reduced CDX1 expression was due to genetic alteration. No CDX1 gene mutations, but two known polymorphisms in exon 1, were observed. LOH was observed in 33% of the tumours investigated but this was not related to CDX1 expression. Since aberrant promoter methylation is a well-known mechanism that participates in gene silencing, the methylation status of the CDX1 5' CpG island promoter was also investigated. PCR amplification of bisulphite-treated DNA followed by cloning was performed in 7 carcinomas that showed low expression of CDX1 and in 1 colonic carcinoma without reduced expression. Promoter hypermethylation occurred in carcinomas in which CDX1 reduced expression was present. These results suggest that CDX1 promoter hypermethylation is one of the molecular mechanisms that accounts for reduced CDX1 gene expression in colorectal carcinoma.

摘要

CDX1同源框基因编码一种在正常小肠和结肠上皮中特异性表达的转录因子,并且在结直肠癌进展过程中CDX1基因表达会受到影响。在本研究中,采用实时定量逆转录聚合酶链反应(RT-PCR)来检测26例结直肠癌中CDX1的表达。与配对的正常结肠黏膜相比,在26例结肠癌中有19例观察到CDX1表达降低:CDX1表达的降低幅度在0.10至0.79之间(降低21%-90%;平均64.75%±22;p = 0.001)。然后采用突变分析和杂合性缺失(LOH)分析来确定CDX1表达降低是否是由于基因改变所致。未观察到CDX1基因突变,但在外显子1中观察到两个已知的多态性。在所研究的肿瘤中有33%观察到LOH,但这与CDX1表达无关。由于异常的启动子甲基化是参与基因沉默的一种众所周知的机制,因此还研究了CDX1 5' CpG岛启动子的甲基化状态。对7例CDX1低表达的癌组织和1例无表达降低的结肠癌组织进行了亚硫酸氢盐处理的DNA的PCR扩增,随后进行克隆。在存在CDX1表达降低的癌组织中发生了启动子高甲基化。这些结果表明,CDX1启动子高甲基化是结直肠癌中CDX1基因表达降低的分子机制之一。

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