Epigenetic inactivation of RASSF1A candidate tumor suppressor gene at 3p21.3 in brain tumors

被引:59
|
作者
Horiguchi, K
Tomizawa, Y
Tosaka, M
Ishiuchi, S
Kurihara, H
Mori, M
Saito, N
机构
[1] Gunma Univ, Sch Med, Dept Neurosurg, Gunma 3718511, Japan
[2] Gunma Univ, Sch Med, Dept Internal Med 1, Gunma 3718511, Japan
关键词
3p21.3; methylation; glioma; medulloblastoma; meningioma; schwannoma;
D O I
10.1038/sj.onc.1207082
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The human Ras association domain family 1A (RASS-F1A) gene, recently isolated from the lung and breast tumor suppressor locus 3p21.3, is highly methylated in primary lung, breast, nasopharyngeal and other tumors, and re-expression of RASSF1A suppresses the growth of several types of cancer cells. Epigenetic inactivation of RASSF1A by promoter hypermethylation is also important in the development of several human cancers. The methylation status of the promoter region of RASSF1A was analysed in primary brain tumors and glioma cell lines by methylation-specific polymerase chain reaction. In primary brain tumors, 25 of 46 ( 54.3%) gliomas and five of five (100%) medulloblastomas showed RASSF1A methylation. In benign tumors, only one of 10 (10%) schwannomas and two of 12 (16.7%) meningiomas showed RASSF1A methylation. The RASSF1A promoter region was methylated in all four glioma cell lines. RASSF1A was re-expressed in all methylated cell lines after treatment with the demethylating agent 5-aza-2'-deoxycytidine. Methylation of the promoter CpG islands of the RASSF1A may play an important role in the pathogenesis of glioma and medulloblastoma.
引用
收藏
页码:7862 / 7865
页数:4
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