Miozzo M, Perotti D, Minoletti F, Mondini P, Pilotti S, Luksch R, Fossati-Bellani F, Pierotti M A, Sozzi G, Radice P
Division of Experimental Oncology A, Istituto Nazionale Tumori, Milan, Italy.
Genomics. 1996 Nov 1;37(3):310-5. doi: 10.1006/geno.1996.0565.
Different findings suggest that alterations of chromosome 7 genes play a role in the development of Wilms tumors. To define the positions of these genes, we have accomplished a combined cytogenetic and molecular study on 11 sporadic Wilms tumors. In one case, where both chromosomes 7 were rearranged, the karyotypic picture was consistent with the presence of a tumor suppressor gene at 7p15. To test this hypothesis, a loss of heterozygosity analysis was performed using microsatellite markers. This revealed a common region of allele losses mapped to the proximal short arm of chromosome 7 and defined the position of the gene(s) involved in Wilms tumors within an interval of approximately 25 cM.
不同的研究结果表明,7号染色体基因的改变在肾母细胞瘤的发生发展中起作用。为了确定这些基因的位置,我们对11例散发型肾母细胞瘤进行了细胞遗传学和分子学联合研究。在1例两条7号染色体均发生重排的病例中,核型图像与7p15存在肿瘤抑制基因一致。为了验证这一假设,使用微卫星标记进行了杂合性缺失分析。这揭示了一个等位基因缺失的共同区域,定位于7号染色体的近端短臂,并在大约25厘摩的区间内确定了与肾母细胞瘤相关的基因位置。