Aberrant MGMT (O6-methylguanine-DNA methyltransferase) promoter methylation in choroid plexus tumors

被引:12
|
作者
Hasselblatt, Martin [1 ]
Muehlisch, Joerg [2 ]
Wrede, Brigitte [3 ]
Kallinger, Birgit [2 ]
Jeibmann, Astrid [1 ]
Peters, Ove [3 ]
Kutluk, Tezer [4 ]
Wolff, Johannes E. A. [5 ]
Paulus, Werner [1 ]
Fruehwald, Michael C. [2 ]
机构
[1] Univ Hosp Munster, Inst Neuropathol, D-48129 Munster, Germany
[2] Univ Childrens Hosp Munster, Dept Pediat Hematol & Oncol, D-48149 Munster, Germany
[3] Univ Regensburg, Dept Pediat Oncol, Regensburg, Germany
[4] Hacettepe Univ, Dept Pediat Oncol, Ankara, Turkey
[5] Univ Texas MD Anderson Canc Ctr, Childrens Canc Hosp, Houston, TX 77030 USA
关键词
Methylation; Temozolomide; Choroid plexus papilloma; Choroid plexus carcinoma; TEMOZOLOMIDE; SURVIVAL; GENES; IDENTIFICATION; CHILDHOOD; FREQUENT; GLIOMAS; BENEFIT; REGION; SPNET;
D O I
10.1007/s11060-008-9694-2
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Aberrant methylation of the MGMT (O6-methylguanine-DNA methyltransferase) DNA-repair gene is a predictive marker for the response to chemotherapy with alkylating agents (e.g., temozolomide) in malignant gliomas. Since temozolomide is considered for the treatment of choroid plexus tumors, MGMT promoter methylation status was retrospectively assessed in 36 choroid plexus tumors using methylation specific PCR, combined bisulfite restriction analysis (COBRA), and clone sequencing. By methylation specific PCR, all samples demonstrated a signal for MGMT methylation. COBRA confirmed > 10% methylation of CpGs 17 and 31 in 58% of tumors. Clone sequencing of six cases methylated by COBRA confirmed aberrant methylation including a previously recognized enhancer element. In conclusion, MGMT promoter methylation is frequent in choroid plexus tumors and can be quantified using COBRA. Determination of MGMT promoter methylation status might be useful for the stratification of patients for alkylator-based treatments in future clinical trials.
引用
收藏
页码:151 / 155
页数:5
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