DNA错配修复缺陷与子宫内膜癌的关系。

Molecular biology international Pub Date : 2011-01-01 Epub Date: 2011-12-08 DOI:10.4061/2011/256063
Kenta Masuda, Kouji Banno, Megumi Yanokura, Yusuke Kobayashi, Iori Kisu, Arisa Ueki, Asuka Ono, Nana Asahara, Hiroyuki Nomura, Akira Hirasawa, Nobuyuki Susumu, Daisuke Aoki
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引用次数: 22

摘要

一些子宫内膜癌病例与家族性肿瘤相关,被称为遗传性非息肉病性结直肠癌(HNPCC或Lynch综合征)。Lynch综合征被认为是由DNA错配修复(MMR)基因的种系突变引起的。MMR基因的畸变阻止了DNA复制过程中产生的碱基错配的准确修复。这种现象可导致参与癌变的靶基因错误频率增加,从而导致细胞癌变。另一方面,异常DNA甲基化被认为在散发性子宫内膜癌发生中起关键作用。与DNA修复相关的癌症相关基因启动子区域中未甲基化的CpG岛的超甲基化导致细胞癌变。因此,在细胞癌变的过程中,遗传和表观遗传的变化错综复杂。本文就DNA错配修复途径在子宫内膜癌中的研究进展作一综述。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Relationship between DNA Mismatch Repair Deficiency and Endometrial Cancer.

Relationship between DNA Mismatch Repair Deficiency and Endometrial Cancer.

Relationship between DNA Mismatch Repair Deficiency and Endometrial Cancer.

Some cases of endometrial cancer are associated with a familial tumor and are referred to as hereditary nonpolyposis colorectal cancer (HNPCC or Lynch syndrome). Lynch syndrome is thought to be induced by germline mutation of the DNA mismatch repair (MMR) gene. An aberration in the MMR gene prevents accurate repair of base mismatches produced during DNA replication. This phenomenon can lead to an increased frequency of errors in target genes involved in carcinogenesis, resulting in cancerization of the cell. On the other hand, aberrant DNA methylation is thought to play a key role in sporadic endometrial carcinogenesis. Hypermethylation of unmethylated CpG islands in the promoter regions of cancer-related genes associated with DNA repair leads to the cell becoming cancerous. Thus, both genetic and epigenetic changes are intricately involved in the process through which cells become cancerous. In this review, we introduce the latest findings on the DNA mismatch repair pathway in endometrial cancer.

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