Wullich B, Müller H W, Fischer U, Zang K D, Meese E
Eur J Cancer. 1993;29A(14):1991-5. doi: 10.1016/0959-8049(93)90460-w.
The met proto-oncogene was found to be amplified in a human glioblastoma cell line (T3095) established from a glioblastoma multiform WHO grade IV. Amplification of epidermal growth factor receptor, transforming growth factor alpha and N-myc which have been described previously in glioblastoma were not observed in T3095. There was, however, an 8-fold met amplification. Giemsa-stained metaphases of T3095 cells revealed multiple (> 5) double minutes (dmins) in the majority of cells. Following xenografting in nude mice there was a significant increase in the number and frequency of dmins. The increase in dmins correlates with the level of met amplification (50-fold), suggesting localisation of the amplified met on dmins. Here we report the first case of met amplification in glioblastoma. Correlation between met amplification and extrachromosomal elements (dmins) has not been reported previously.
在源自世界卫生组织IV级多形性胶质母细胞瘤的人胶质母细胞瘤细胞系(T3095)中发现原癌基因met被扩增。在T3095中未观察到先前在胶质母细胞瘤中描述过的表皮生长因子受体、转化生长因子α和N-myc的扩增。然而,met有8倍的扩增。T3095细胞的吉姆萨染色中期显示大多数细胞中有多个(>5个)双微体(dmins)。在裸鼠中进行异种移植后,dmins的数量和频率显著增加。dmins的增加与met扩增水平(50倍)相关,提示扩增的met定位于dmins上。在此我们报告胶质母细胞瘤中met扩增的首例病例。met扩增与染色体外元件(dmins)之间的相关性此前未见报道。