Sugawa N, Ekstrand A J, Ueda S, Collins V P
Department of Pathology I, Sahlgrenska Hospital.
Noshuyo Byori. 1993;10(2):161-3.
Loss of genetic information from a number of specific regions of the genome has been documented in primary human gliomas. Recently loss of heterozygosity or nullizygosity of the IFN beta 1 gene has been found in glioblastomas. We used Restriction Fragment Length Polymorphism (RFLP) analysis in order to screen the frequency of the loss of this genes in glial tumors of malignancy grades I-IV. Nullizygosity for IFN beta 1 was detected in 8/30 (27%) of glioblastomas (malignancy grade IV) and loss of heterozygosity in a further two cases (7%). In total, 33% of these tumors lost least one copy of the IFN beta 1 gene. Among the 10 anaplastic gliomas (grade III), 2 (20%) showed loss of one copy of the gene which none of the 7 low grade gliomas (grades I or II) showed any evidence of loss of IFN beta 1 alleles. The loss of the IFN beta 1 gene would appear to be a late event associated with the development of an increasingly malignant phenotype in human gliomas and to be confined to gliomas of malignancy grade III or IV.
原发性人类胶质瘤中已发现基因组多个特定区域的遗传信息丢失。最近,在胶质母细胞瘤中发现了IFNβ1基因杂合性缺失或纯合性缺失。我们使用限制性片段长度多态性(RFLP)分析来筛查该基因在I-IV级恶性胶质瘤中的缺失频率。在8/30(27%)的胶质母细胞瘤(IV级恶性肿瘤)中检测到IFNβ1纯合性缺失,另外2例(7%)出现杂合性缺失。这些肿瘤中总计33%至少丢失了一个IFNβ1基因拷贝。在10例间变性胶质瘤(III级)中,2例(20%)显示一个基因拷贝丢失,而7例低级别胶质瘤(I级或II级)均未显示出IFNβ1等位基因丢失的任何证据。IFNβ1基因的丢失似乎是一个晚期事件,与人类胶质瘤中恶性表型的逐渐发展相关,并且仅限于III级或IV级恶性胶质瘤。