Zhang S J, Endo S, Ichikawa T, Washiyama K, Kumanishi T
Department of Molecular Neuropathology, Brain Research Institute, Niigata University, Japan.
Cancer Res. 1998 Mar 15;58(6):1231-7.
A total of 10 primary malignant lymphomas of the brain were examined for deletion, mutation, and 5' CpG island methylation of the p16 gene, which is a candidate tumor suppressor gene with CDK-inhibitory function. In Southern blot analysis, p16 gene deletion was suggested in nine cases, homozygously (five cases) or hemizygously (four cases). In the remaining one case, p16 gene deletion was not suggested. Although single-strand conformation polymorphism and nucleotide analyses suggested no mutations of the p16 gene in these cases, methylation analyses revealed 5' CpG island methylation in three cases, of which two were those with presumed hemizygous deletion and one was that without deletion in Southern blot analysis. Thus, p16 gene abnormality was detected in all 10 of the brain lymphomas examined, and in 8 of them, actual p16 gene inactivation was suggested by their homozygous deletion (5 cases) or 5' CpG island methylation (3 cases). These findings suggest that p16 gene abnormality and inactivation are closely related to carcinogenesis in primary malignant lymphoma of the brain. The p15 gene, another candidate tumor suppressor gene located in the vicinity of the p16 gene, to which it shows structural and functional similarity, was also presumed to be deleted similarly in most cases. Its methylation was seen in one case, the case without the methylated p16 gene.
对总共10例原发性脑恶性淋巴瘤进行了检测,分析其p16基因的缺失、突变及5' CpG岛甲基化情况。p16基因是一种具有细胞周期蛋白依赖性激酶(CDK)抑制功能的候选抑癌基因。在Southern印迹分析中,9例提示有p16基因缺失,其中纯合缺失(5例)或半合子缺失(4例)。其余1例未提示有p16基因缺失。尽管单链构象多态性和核苷酸分析提示这些病例中p16基因无突变,但甲基化分析显示3例存在5' CpG岛甲基化,其中2例为推测有半合子缺失的病例,1例为Southern印迹分析中无缺失的病例。因此,在所检测的全部10例脑淋巴瘤中均检测到p16基因异常,其中8例通过纯合缺失(5例)或5' CpG岛甲基化(3例)提示存在实际的p16基因失活。这些发现提示p16基因异常和失活与原发性脑恶性淋巴瘤的致癌作用密切相关。p15基因是另一种候选抑癌基因,位于p16基因附近,与其在结构和功能上具有相似性,推测在大多数病例中也同样发生缺失。在1例病例中观察到其甲基化,该病例中p16基因未发生甲基化。