摘要
目的探讨急性非淋巴细胞白血病(ANLL)中降钙素基因(CT基因)的甲基化状况及其意义。方法利用限制性内切酶和聚合酶链反应(PCR)技术。结果25例ANLL患者中18例检测到CT基因高度甲基化,阳性率72%,而且实验的敏感性至少达到10-3水平,结论CT基因高度甲基化较普遍地存在于ANLL,可作为AN-LL恶性细胞的分子标志,用于ANLL患者治疗后微小残留病(MRD)的检测,以利于预测复发、指导治疗和评价疗效。
Objective To study the methylation pattern of calcitonin gene (CT gene) in acute nonlymphoblastic leukemia(ANLL)and ist implication. Methods By using restriction endonuclease and polymerase chain reaction(PCR) techniques. Results The positive rate was 72%.And the sensitivity of this method was at least 3 logs (1 in 1 000).Conclusion This findings indicated that the hypermethlation of CT gene was common in ANLL.It might be used as a molecular marker for the tumor cells in ANLL. So that,it can serve as a useful tool for detection of minimal residual disease(MRD) in ANLL to predict early relapase, to guide the treatment and to evaluate the effectiveness of therapy.
出处
《白血病》
1999年第1期33-35,共3页
关键词
急性
白血病
降钙素基因
甲基化
PCR
Acute nonlymphoblastic leukemia Calcitonin gene Methylation Polymerase chain reaction Minimal residual disease