Oberstrass J, Ring G U, Vogeley K T, Kramm C M, Cobbers J M, Wirths J, Bilzer T, Wechsler W
Institut für Neuropathologie, Heinrich-Heine-Universität, Düsseldorf.
Verh Dtsch Ges Pathol. 1994;78:413-7.
Loss of genetic material on chromosome 10 is regarded as a prominent feature in the genesis of glioblastomas. To use chromosome 10 deletions as diagnostic markers for glioblastomas we investigated, if the loss of chromosome 10 material could be restricted on the region 10q21-26. By PCR microsatellite analysis on frozen tissue and paraffin material from the ZULCH brain tumor collection we found (1) loss of heterozygosity in 10q21-26 in 75% of the investigated DNA from frozen tissue and (2) an interstitial loss in the region of the microsatellite marker D10S186. The combined immunohistochemical analysis of overexpression of EGFR, EGF and TGF alpha with LOH on chromosome 10 showed that chromosome 10 deletions are not exclusively bound to EGFR overexpression.
10号染色体上遗传物质的缺失被视为胶质母细胞瘤发生过程中的一个显著特征。为了将10号染色体缺失用作胶质母细胞瘤的诊断标志物,我们研究了10号染色体物质的缺失是否局限于10q21 - 26区域。通过对ZULCH脑肿瘤样本库中冷冻组织和石蜡材料进行PCR微卫星分析,我们发现:(1)在75%的冷冻组织检测DNA中,10q21 - 26区域存在杂合性缺失;(2)微卫星标记D10S186区域存在中间缺失。对EGFR、EGF和TGFα过表达与10号染色体杂合性缺失进行联合免疫组化分析,结果显示10号染色体缺失并不完全与EGFR过表达相关。