Baik J H, Griffiths S, Giuili G, Manson M, Siegrist S, Guellaen G
Unité INSERM 99, Hôpital Henri Mondor, Creteil, France.
Carcinogenesis. 1991 Jun;12(6):1035-9. doi: 10.1093/carcin/12.6.1035.
The methylation status of the rat gamma-glutamyl transpeptidase (GGT) gene was investigated during liver development and hepatocarcinogenesis. The analysis with the restriction enzymes MspI/HpaII revealed that, during ontogeny, there is a progressive methylation of the GGT gene that coincides with a progressive decrease in GGT activity. Thus, there is an inverse correlation between methylation and expression of the GGT gene, suggesting a role for DNA methylation in the regulation of the gene during normal differentiation. The methylation patterns of the GGT gene in liver tumours induced by aflatoxin B1 exhibit heterogeneity. Nevertheless, a band of 5.7 kb was observed in all the DNA samples from aflatoxin B1-induced tumours which was not present in control liver DNA. The specificity of the DNA methylation changes was assessed using nafenopin, which induces hepatic tumours without elevation of GGT activity. We conclude that, during hepatocarcinogenesis, there is a modification of the DNA methylation pattern of the GGT gene, but there is no simple correlation with GGT activity. In no case was the GGT gene methylation in hepatocarcinogenesis found to be equivalent to the pattern observed in fetal liver. Thus if methylation is involved in the regulation of GGT gene transcription, the mechanisms must be different in fetal liver and hepatocarcinoma.
在肝脏发育和肝癌发生过程中,对大鼠γ-谷氨酰转肽酶(GGT)基因的甲基化状态进行了研究。用限制性内切酶MspI/HpaII分析表明,在个体发育过程中,GGT基因存在逐渐甲基化的现象,这与GGT活性的逐渐降低相吻合。因此,GGT基因的甲基化与表达呈负相关,提示DNA甲基化在正常分化过程中对该基因的调控发挥作用。黄曲霉毒素B1诱导的肝肿瘤中GGT基因的甲基化模式表现出异质性。然而,在所有来自黄曲霉毒素B1诱导肿瘤的DNA样本中均观察到一条5.7 kb的条带,而对照肝脏DNA中不存在该条带。使用萘酚平评估DNA甲基化变化的特异性,萘酚平诱导肝肿瘤但不升高GGT活性。我们得出结论,在肝癌发生过程中,GGT基因的DNA甲基化模式发生了改变,但与GGT活性没有简单的相关性。在任何情况下,肝癌发生过程中的GGT基因甲基化都与胎儿肝脏中观察到的模式不同。因此,如果甲基化参与了GGT基因转录的调控,那么胎儿肝脏和肝癌中的机制必定不同。