Hiyama E, Hiyama K, Yokoyama T
Department of General Medicine, Hiroshima University School of Medicine, Japan.
Cancer Res. 1991 Apr 1;51(7):1946-51.
We detected a rearrangement in the N-myc gene region in a neuroblastoma from a 9-month-old girl. In this case, the N-myc gene was amplified 50-fold in the primary tumor, the lymph node metastasis, and the hepatic metastasis. The rearrangement was detected only in the primary tumor and the lymph node metastasis, whereas N-myc RNA and protein expression were detected only in the primary tumor and the hepatic metastasis. Both the rearranged N-myc gene and the normal N-myc gene were amplified 25-fold, and the rearrangement occurred 723 nucleotides downstream from the 3' end of exon 3. The cell line (NH-6) derived from the primary tumor showed N-myc gene amplification without this rearrangement. These results suggest the following: (a) the primary tumor had a least two clones; (b) the rearrangement interrupted N-myc gene expression; and (c) oncogenesis preceded N-myc gene amplification.
我们在一名9个月大女童的神经母细胞瘤中检测到N-myc基因区域重排。在此病例中,原发肿瘤、淋巴结转移灶及肝转移灶中的N-myc基因均扩增了50倍。重排仅在原发肿瘤和淋巴结转移灶中检测到,而N-myc RNA和蛋白表达仅在原发肿瘤和肝转移灶中检测到。重排的N-myc基因和正常N-myc基因均扩增了25倍,重排发生在外显子3 3'端下游723个核苷酸处。源自原发肿瘤的细胞系(NH-6)显示N-myc基因扩增但无此重排。这些结果提示如下:(a)原发肿瘤至少有两个克隆;(b)重排中断了N-myc基因表达;(c)肿瘤发生先于N-myc基因扩增。