MGMT启动子甲基化对神经胶质瘤患者治疗及预后的临床意义

The clinical significance of MGMT promoter methylation in the treatment and prognosis of glioma patients

  • 摘要: 目前以替莫唑胺(temozolomide,TMZ)为基础的化疗已成为神经胶质瘤术后辅助治疗的标准方案,然而TMZ对部分患者疗效欠佳。DNA修复蛋白O6-甲基鸟嘌呤-DNA甲基转移酶(O6-methylguanine-DNA methyltransferase,MGMT)启动子甲基化是胶质瘤患者的重要分子标志物,与胶质瘤预后及烷基化药物如TMZ的耐药有关。在新诊断的胶质母细胞瘤中,MGMT启动子甲基化已成为独立预后指标。MGMT启动子甲基化是抑制MGMT蛋白表达的关键机制,可抑制DNA修复,增加TMZ化疗敏感性。本文综述了MGMT启动子甲基化与神经胶质瘤患者预后、疗效的最新数据及临床试验,对MGMT启动子甲基化在临床中的应用进行总结,以期为神经胶质瘤患者的个体化治疗提供参考。

     

    Abstract: Adjuvant temozolomide- based chemotherapy has become the standard of care for most postoperative glioma patients. However, a large proportion of these patients do not respond to temozolomide. DNA repair enzyme O6-methylguanine-DNA methyltransferase (MGMT) promoter methylation has emerged as an important molecular marker in patients with gliomas. It is associated with prognosis and resistance to alkylated drugs such as temozolomide. MGMT promoter methylation is the key mechanism of MGMT gene silencing, thereby inhibiting DNA repair and increasing the sensitivity of chemotherapy. We reviewed current data on the prognostic and predictive relevance of MGMT testing and clinical trials, summarized the clinical application of MGMT promoter methylation, in order to provide reference for the individualized treatment of glioma patients.

     

/

返回文章
返回