Department of Obstetrics and Gynecology, School of Medicine, Keio University, Tokyo, Japan.
Int J Oncol. 2012 Sep;41(3):793-7. doi: 10.3892/ijo.2012.1528. Epub 2012 Jun 25.
Epimutation is defined as abnormal transcriptional repression of active genes and/or abnormal activation of usually repressed genes caused by errors in epigenetic gene repression. Epimutation arises in somatic cells and the germline, and constitutional epimutation may also occur. Epimutation is the first step of tumorigenesis and can be a direct cause of carcinogenesis. Cancers associated with epimutation include Lynch syndrome (hereditary non-polyposis colorectal cancer, HNPCC), chronic lymphocytic leukemia, breast cancer and ovarian cancer. Epimutation has been shown for many tumor suppressor genes, including RB, VHL, hMLH1, APC and BRCA1, in sporadic cancers. Methylation has recently been shown in DNA from normal tissues and peripheral blood in cases of sporadic colorectal cancer and many studies show constitutive epimutation in cancers. Epimutation of DNA mismatch repair (MMR) genes (BRCA1, hMLH1 and hMSH2) involved in development familial cancers has also been found. These results have led to a focus on epimutation as a novel oncogenic mechanism.
表观突变被定义为由于表观基因抑制错误而导致的活性基因的异常转录抑制和/或通常受抑制的基因的异常激活。表观突变发生在体细胞和生殖细胞中,也可能发生构成性表观突变。表观突变是肿瘤发生的第一步,也可能是致癌的直接原因。与表观突变相关的癌症包括林奇综合征(遗传性非息肉病性结直肠癌,HNPCC)、慢性淋巴细胞白血病、乳腺癌和卵巢癌。在散发性癌症中,许多肿瘤抑制基因,包括 RB、VHL、hMLH1、APC 和 BRCA1,已被证明存在表观突变。最近在散发性结直肠癌的正常组织和外周血的 DNA 中也发现了甲基化,许多研究表明癌症中存在构成性表观突变。在涉及家族性癌症的 DNA 错配修复(MMR)基因(BRCA1、hMLH1 和 hMSH2)中也发现了表观突变。这些结果导致人们关注表观突变为一种新的致癌机制。