Balaban G, Gilbert F, Nichols W, Meadows A T, Shields J
Cancer Genet Cytogenet. 1982 Jul;6(3):213-21. doi: 10.1016/0165-4608(82)90058-9.
Constitutional chromosome abnormalities have been associated with retinoblastoma, Wilm's tumor, and a familial form of renal carcinoma. For each tumor type, the particular chromosome segment involved in the observed rearrangements is different: in retinoblastoma, that segment is band q14 on chromosome #13. We now present evidence that in retinoblastoma, structural abnormalities involving the particular chromosome segment identified in the constitutional cases can also occur in the tumors of individuals with normal constitutional karyotypes. Six cases with retinoblastoma in one or both eyes were analyzed; deletions/rearrangements involving 13q14 were found in the tumor cell karyotypes of five of the six. These observations suggest that changes in a gene or genes at a common site (13q14) play a role in tumorigenesis in all forms of retinoblastoma, sporadic as well as heritable.
染色体结构异常与视网膜母细胞瘤、肾母细胞瘤以及一种家族性肾癌有关。对于每种肿瘤类型,在观察到的重排中涉及的特定染色体片段是不同的:在视网膜母细胞瘤中,该片段是13号染色体上的q14带。我们现在提供证据表明,在视网膜母细胞瘤中,涉及在染色体结构正常个体的肿瘤中也可出现涉及在染色体结构异常病例中所确定的特定染色体片段的结构异常。分析了6例单眼或双眼患视网膜母细胞瘤的病例;6例中有5例的肿瘤细胞核型中发现有涉及13q14的缺失/重排。这些观察结果表明,一个或多个位于共同位点(13q14)的基因的改变在所有形式的视网膜母细胞瘤(散发性和遗传性)的肿瘤发生中起作用。