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出 处:《中华肿瘤杂志》1998年第6期412-414,共3页Chinese Journal of Oncology
基 金:卫生部青年基金
摘 要:目的分析Rb基因表达异常原因,研究Rb基因启动子甲基化状态和甲基苄基亚硝胺(NMBzA)对Rb基因启动子的影响。方法采用限制性核酸内切酶酶切和PCR扩增方法。结果33.3%的食管癌组织Rb基因启动子存在MspⅠ型高甲基化,40.0%的食管癌组织Rb基因启动子存在HpaⅡ型高甲基化。1例标本存在MspⅠ和HpaⅡ两种类型的高甲基化。恒河猴1次灌喂30mg/kgNMBzA后1,2,3天,其食管上皮Rb基因启动子HpaⅡ、MspⅠ类型甲基化逐渐增强;第5天其Rb基因启动子HpaⅡ、MspⅠ类型甲基化程度明显下降。结论食管癌组织中Rb基因表达异常可能与启动子高甲基化有关,NMBzA通过启动子甲基化对Rb基因调控产生影响。Objective To elucidate the cause of abnormal Rb expression in esophageal cancer (EC). Methods Methylation of Rb gene promoter was examined with restriction endonuclease digestion and PCR amplification. Results Of the 30 specimens of EC, 10 (33.3%) had MspⅠ type hypermethylation of the Rb gene promoter while 12 (40.0%) had HpaⅡ type hypermethylation and one had both type of hypermethylation. In monkey fed with a single dose of NMBzA (30 mg/kg) on day 0, increasing hypermethylation of both types of the Rb gene promoter in esophageal epithelium was found on day 1,2 and 3 but reduced on day 5. Conclusion These data suggest that abnoromal expression of Rb gene may be related to hypermethylation of its promoter and carcinogen NMBzA can induce such hypermethylation in monkey esophageal epithelium.
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