Bentz M, Bergerheim U S, Li C, Joos S, Werner C A, Baudis M, Gnarra J, Merino M J, Zbar B, Linehan W M, Lichter P
Deutsches Krebsforschungszentrum, Abt. Organisation komplexer Genome, Heidelberg, Germany.
Cytogenet Cell Genet. 1996;75(1):17-21. doi: 10.1159/000134448.
We used comparative genomic hybridization to analyze 17 tumor samples from 11 patients with papillary renal cell carcinoma (RCC), including three patients with hereditary papillary RCC. Whereas the most frequent aberrations confirmed data obtained by banding analyses, copy number increases on 5q, which previously were considered characteristic of nonpapillary RCC, were identified in two cases. In two complex cases belonging to the same family, a characteristic pattern of chromosomal aberrations was found: five of the six imbalances present in the less complex case were included in the karyotype of the other case, suggesting a genetically determined mechanism resulting in genomic instability of specific chromosomes or chromosomal subregions and/or selection of specific mutations.
我们使用比较基因组杂交技术分析了11例乳头状肾细胞癌(RCC)患者的17个肿瘤样本,其中包括3例遗传性乳头状RCC患者。虽然最常见的畸变证实了通过染色体显带分析获得的数据,但在两例病例中发现了5号染色体长臂的拷贝数增加,此前认为这是非乳头状RCC的特征。在属于同一家族的两例复杂病例中,发现了一种特征性的染色体畸变模式:较简单病例中存在的6种失衡中的5种包含在另一病例的核型中,这表明存在一种遗传决定机制,导致特定染色体或染色体亚区域的基因组不稳定和/或特定突变的选择。