Gonzalez-Gomez P, Bello M J, Alonso M E, Arjona D, Lomas J, de Campos J M, Isla A, Rey J A
Departmento de C. Experimental, Laboratorio de Oncogenetica Molecular, Hospital Universitario La Paz, Madrid, Spain.
Br J Cancer. 2003 Jan 13;88(1):109-14. doi: 10.1038/sj.bjc.6600737.
A series of 136 nervous system tumours were studied to determine the methylation status of the CpG island contained within the promoter region of the RB1 gene, as well as mutation analysis of the essential promoter region and exons 20-24 (and surrounding intronic regions) coding for the protein-binding pocket domain. Methylation of the RB1 CpG island was detected in 26 samples corresponding to nine glioblastomas, three anaplastic astrocytomas, one mixed oligo-astrocytoma, one ependymoma, two medulloblastomas, two primary central nervous system lymphomas, two neurofibrosarcomas, and six brain metastasis from solid tumours. No inactivating mutations were found within the RB1 promoter region, whereas one glioblastoma and one oligodendroglioma displayed similar sequence variations consisting of 12 and 8 base pair deletions at intron 21. These results suggest that RB1 CpG island hypermethylation is a common epigenetic event that is associated with the development of malignant nervous system tumours.
对136例神经系统肿瘤进行了研究,以确定RB1基因启动子区域内CpG岛的甲基化状态,以及对编码蛋白质结合口袋结构域的基本启动子区域和外显子20 - 24(以及周围内含子区域)进行突变分析。在26个样本中检测到RB1 CpG岛甲基化,这些样本对应9例胶质母细胞瘤、3例间变性星形细胞瘤、1例混合性少突星形细胞瘤、1例室管膜瘤、2例髓母细胞瘤、2例原发性中枢神经系统淋巴瘤、2例神经纤维肉瘤以及6例实体瘤脑转移瘤。在RB1启动子区域未发现失活突变,而1例胶质母细胞瘤和1例少突胶质细胞瘤显示出相似的序列变异,在内含子21处分别有12和8个碱基对的缺失。这些结果表明,RB1 CpG岛高甲基化是一种常见的表观遗传事件,与恶性神经系统肿瘤的发生有关。