Reeve A E, Housiaux P J, Gardner R J, Chewings W E, Grindley R M, Millow L J
Nature. 1984;309(5964):174-6. doi: 10.1038/309174a0.
Genomic changes within chromosome band 11p13 appear to have a role in the initiation of Wilms' tumour. The human Harvey ras oncogene, c-Ha-ras 1, has been located by Jhanwar et al. immediately adjacent to this region at band 11p14 .1, although several groups have assigned the gene more distally at band 11p15 . We have examined tumour DNA from two cases of sporadic Wilms' tumour, and report here that in both cases one of the two constitutional c-Ha-ras 1 alleles was absent. One tumour had a reciprocal translocation between the short arm of chromosome 11 (at band 11p13), and the long arm of chromosome 12, with no visible loss of chromosomal material. The loss of a c-Ha-ras 1 allele in association with this translocation indicates that a submicroscopic deletion had occurred. The resulting hemizygosity may have had a role in tumour initiation. Our results indicate that the c-Ha-ras 1 gene and the 'Wilms' tumour locus' may be in close proximity. It would, therefore, be premature to exclude the possibility that these two sites are functionally related.
11号染色体11p13带内的基因组变化似乎在肾母细胞瘤的起始过程中发挥作用。人类哈维ras癌基因c-Ha-ras 1已被Jhanwar等人定位在紧邻该区域的11p14.1带,不过有几个研究小组将该基因定位在更远处的11p15带。我们检测了两例散发性肾母细胞瘤的肿瘤DNA,并在此报告,在这两例病例中,两个组成性c-Ha-ras 1等位基因中的一个缺失。其中一个肿瘤在11号染色体短臂(11p13带)和12号染色体长臂之间发生了相互易位,未见染色体物质明显丢失。与这种易位相关的c-Ha-ras 1等位基因缺失表明发生了亚显微缺失。由此产生的半合子状态可能在肿瘤起始中起作用。我们的结果表明,c-Ha-ras 1基因与“肾母细胞瘤位点”可能紧密相邻。因此,排除这两个位点在功能上相关的可能性还为时过早。