Glavac D, Ravnik-Glavac M, Ovcak Z, Masera A
National Institute of Chemistry, Ljubljana, Slovenia.
Pflugers Arch. 1996;431(6 Suppl 2):R193-4. doi: 10.1007/BF02346334.
64 kidney tumours of clear cell histopathology were analysed with non-isotopic SSCP and HA for the presence of VHL gene defects. All positive cases were further characterised by direct sequencing. In 30 tumours (48%) mutations were identified in the coding region of the VHL gene. Other tumours were examined for methylation changes in 5' CpG islands in exon 1 Bisulphite genomic sequencing which gives positive signal for methylated cytosines, was used in this analysis and in 7 tumours hypermethylation of 5' CpG islands was found. These findings suggest that VHL gene mutations together with methylation associated inactivation of the VHL gene are important events that predispose to renal cell tumorigenesis.
采用非同位素单链构象多态性(SSCP)和杂合性分析(HA)对64例透明细胞组织病理学类型的肾肿瘤进行VHL基因缺陷检测。所有阳性病例均通过直接测序进一步鉴定。在30个肿瘤(48%)中,VHL基因编码区发现了突变。对其他肿瘤检测了外显子1中5' CpG岛的甲基化变化,该分析采用亚硫酸氢盐基因组测序(其对甲基化胞嘧啶给出阳性信号),在7个肿瘤中发现了5' CpG岛的高甲基化。这些发现表明,VHL基因突变以及与VHL基因甲基化相关的失活是导致肾细胞肿瘤发生的重要事件。