Yamazaki H, Fukui Y, Ueyama Y, Tamaoki N, Kawamoto T, Taniguchi S, Shibuya M
Department of Genetics, University of Tokyo, Japan.
Mol Cell Biol. 1988 Apr;8(4):1816-20. doi: 10.1128/mcb.8.4.1816-1820.1988.
By using Southern blot analysis, we found that in two cases of human glioblastoma multiforme, cells carried amplified c-erbB genes which bore short deletion mutations within the ligand-binding domain of the epidermal growth factor (EGF) receptor. The products of these mutated c-erbB genes were about 30 kilodalton (kDa) smaller than the normal 170-kDa EGF receptor, and the tumor cell membrane fractions containing the 140-kDa abnormal EGF receptor showed a significant elevation of tyrosine kinase activity without its ligand. In view of the similarity to the activated viral and cellular erbB genes in the avian system, these mutated and overexpressed EGF receptors might play a role in the onset or development of human glioblastoma cells.
通过Southern印迹分析,我们发现在两例多形性胶质母细胞瘤中,细胞携带扩增的c-erbB基因,这些基因在表皮生长因子(EGF)受体的配体结合域内存在短缺失突变。这些突变的c-erbB基因产物比正常的170 kDa EGF受体小约30千道尔顿(kDa),并且含有140 kDa异常EGF受体的肿瘤细胞膜组分在没有其配体的情况下显示出酪氨酸激酶活性的显著升高。鉴于与禽类系统中活化的病毒和细胞erbB基因的相似性,这些突变和过表达的EGF受体可能在人胶质母细胞瘤细胞的发生或发展中起作用。