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人结直肠癌中Myf-3基因的高甲基化

Hypermethylation of the Myf-3 gene in human colorectal cancer.

作者信息

Iacopetta B J, Harmon D, Spagnolo D V, House A K, Kay P H

机构信息

Department of Surgery, University of Western Australia, Nedlands, Australia.

出版信息

Anticancer Res. 1997 Jan-Feb;17(1A):429-32.

PMID:9066689
Abstract

Abnormal methylation of DNA is one of the earliest detectable changes in human tumors. We investigated hypermethylation of the Myf-3 gene, the human homolog of the mouse myogenic gene Myo-D1, in colorectal adenomas and adenocarcinomas. Histologically normal gut mucosa from colorectal cancer patients showed moderately higher levels of methylation than in other normal tissues. Varying degrees of Myf-3 hypermethylation were found in all five adenomas and eight adenocarcinomas examined. Carcinomas arising from within adenomas generally showed a decrease in both the heterogeneity and intensity of Myf-3 methylation. Regional hypermethylation of this gene therefore appears to be an early event in human colorectal neoplasia.

摘要

DNA异常甲基化是人类肿瘤中最早可检测到的变化之一。我们研究了人源肌生成基因Myf-3(小鼠肌生成基因Myo-D1的同源基因)在结直肠腺瘤和腺癌中的高甲基化情况。结直肠癌患者组织学正常的肠黏膜显示出比其他正常组织中略高的甲基化水平。在所检测的全部5个腺瘤和8个腺癌中均发现了不同程度的Myf-3高甲基化。由腺瘤发展而来的癌通常在Myf-3甲基化的异质性和强度方面均有所降低。因此,该基因的区域高甲基化似乎是人类结直肠肿瘤形成过程中的早期事件。

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