A review of the alterations in DNA methylation in esophageal squamous cell carcinoma

被引:52
|
作者
Baba, Yoshifumi [1 ]
Watanabe, Masayuki [1 ]
Baba, Hideo [1 ]
机构
[1] Kumamoto Univ, Grad Sch Med Sci, Dept Surg Gastroenterol, Kumamoto 8608556, Japan
基金
日本学术振兴会;
关键词
Epigenetics; Methylation; LINE-1; Esophageal cancer; CPG ISLAND HYPERMETHYLATION; TUMOR-SUPPRESSOR GENE; LYMPH-NODE METASTASIS; E-CADHERIN EXPRESSION; HISTIDINE TRIAD GENE; PROMOTER HYPERMETHYLATION; MICROSATELLITE INSTABILITY; ABERRANT METHYLATION; POOR-PROGNOSIS; PROTEIN EXPRESSION;
D O I
10.1007/s00595-012-0451-y
中图分类号
R61 [外科手术学];
学科分类号
摘要
Epigenetic changes such as DNA methylation, histone modification, and loss of genome imprinting play a crucial role in esophageal squamous cell carcinogenesis, along with genomic and genetic alterations. DNA methylation is a fundamental epigenetic process that modulates gene expression. Cancer cells exhibit two types of alterations of DNA methylation: global DNA hypomethylation and site-specific CpG island promoter hypermethylation. In several types of human cancers, the methods of detecting an aberrant methylation status have been applied to clinical fields to stratify high-risk groups, detect early cancer, and predict clinical outcomes. Importantly, epigenetic changes, including alterations in DNA methylation, are reversible and can thus be targets for cancer therapy or chemoprevention. Therefore, a better understanding of the DNA methylation in esophageal squamous cell carcinoma (ESCC) is important for optimizing cancer therapy and chemoprevention. We herein summarize the current knowledge regarding alterations in DNA methylation and the clinical implications in ESCC.
引用
收藏
页码:1355 / 1364
页数:10
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