Issa J P, Ottaviano Y L, Celano P, Hamilton S R, Davidson N E, Baylin S B
Oncology Center, Johns Hopkins University Medical Institutions, Baltimore, Maryland 21205.
Nat Genet. 1994 Aug;7(4):536-40. doi: 10.1038/ng0894-536.
We report that CpG island methylation, an epigenetic modification of DNA known to correlate closely with silencing of gene transcription, appears in the oestrogen receptor (ER) gene in a subpopulation of cells which increases as a direct function of age in human colonic mucosa. This same methylation change characterizes virtually all cells in all 45 colorectal tumours examined, including the earliest stages of tumour formation. ER gene expression is diminished or absent in colorectal tumours, and introduction of an exogenous ER gene in cultured colon carcinoma cells resulted in marked growth suppression. Our data suggest that methylation associated inactivation of the ER gene in ageing colorectal mucosa could be one of the earliest events that predispose to sporadic colorectal tumorigenesis.
我们报告称,CpG岛甲基化作为一种已知与基因转录沉默密切相关的DNA表观遗传修饰,出现在人类结肠黏膜中一部分细胞的雌激素受体(ER)基因中,且这部分细胞会随着年龄的增长而直接增加。在所有检测的45个结直肠癌肿瘤中,包括肿瘤形成的最早阶段,几乎所有细胞都有这种相同的甲基化变化。结直肠癌肿瘤中ER基因表达减少或缺失,并且在培养的结肠癌细胞中引入外源性ER基因会导致明显的生长抑制。我们的数据表明,在衰老的结肠黏膜中,与ER基因甲基化相关的失活可能是易患散发性结直肠癌的最早事件之一。