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非何杰金淋巴瘤P15基因甲基化和去甲基化再表达的研究

Study on P15 Gene Methlation and Reexpression by Demethylation in Non-Hodgkin’s Lymphomas

【作者】 周涛

【导师】 郭秀枝;

【作者基本信息】 暨南大学 , 内科学, 2000, 硕士

【摘要】 P15基因是肿瘤抑制基因的候选基因,受细胞生长抑制蛋白FGF-β的诱导,编码周期素依赖激酶4/6(CDK4/6)抑制因子,对细胞周期起负调控作用,P15基因操纵区5’-CpG岛的甲基化被认为是基因缺失之外的又一失活机制。P15基因5’-CpG岛的异常甲基化导致该基因转录的抑制,5-杂氮脱氧胞嘧啶(5-Aza-2cdR)通过共价俘获DNA甲基转移酶抑制DNA的甲基化,使因甲基化失活的生长调控基因重新激活并表达。本文用甲基化特异性PCR(MSP)的方法以亚硫酸氢钠修饰后的DNA为模扳,检测了32例非杰何金淋巴瘤石蜡标本P15基因甲基化,用5-Aza-2cdR诱导非何杰金淋巴瘤raji细胞株P15基因去甲基化,结合RT-PCR方法测定诱导前后P15基因的表达,结果提示:非何杰金淋巴瘤P15基因操纵区甲基化的发生率为18.75%(6/32),高度恶性比低度恶性更易发生甲基化,其发生率分别为31.6%和0%。在5-Aza-2cdR10-7-10-6mol/L浓度时P15基因可去甲基化再表达。并且raji细胞生长显著抑制,停留G0/G1期细胞数升高近2倍。结果表明:5-Aza-2cdR可通过P15基因去甲基化再表达抑制raji细胞的生长,为恶性血液病去甲基化临床治疗提供实验依据。

【Abstract】 P15 gene is a candidate as tumor suppressor gene. As cell cycle negative regulator, it is a inhibitor of cyclin-dependent kinase CDK4 and CDK6,whose expression is induced by transforming growth factor(TGF-β)which is a potent inhibitor of cell growth . Abberrant methylation of 5’-CpG islands of P15 gene promoter has been recently described as an alternative mechanism of gene inactivation besides gene deletion. 5’-Aza-2cdR, which can inhibit DNA methylation by covalently traping DNA methylases as their target site in DNA, plays a role in demethylation and reactivate growth-regulator gene inactivated by demethylation. Using a recently found method that methylation-specific ploymerose chain reaction (MSP) is preceded by bisulfite modification of DNA, we investigated the methylation status of 32 NHL cases and raji cell lines of non-Hodgkin’s lymphoma (NHL) induced by 5-Aza-2cdR, and investigated the P15 gene reexpression of raji cell lines before and after induced by 5-Aza-2cdR by RT-PCR.The results have showed that 18.75% (6/32) in NHL is methylation in P15 gene,and methylation was much more frequently in high grade malignant NHL patients 31.6% than in low grade malignant patients 0%. P15 gene can be demethylated and reexpressed with 5-Aza-2cdR of 10-7-10-6 mollL concentration so that inhibited the growth of rajicell lines and resulted in about 2-fold increase in the proportion of cells in G1\G0.The results have also suggested that 5-Aza-2cdR can inhibit the raji cell growth by inducing the reexpression of P15 gene.The method of P15 gene of demethylation provides an experimental foundation for hematologic malignant clincal therapy.

【关键词】 P15基因高甲基化MSP去甲基化再表达
【Key words】 P15genehypermethylationMSPdemethylationreexpression
  • 【网络出版投稿人】 暨南大学
  • 【网络出版年期】2002年 01期
  • 【分类号】R733.1
  • 【被引频次】1
  • 【下载频次】55
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