Rigola Maria Angels, Casadevall Carme, Bernués Marta, Caballín Maria Rosa, Fuster Carme, Gelabert Antoni, Egozcue Josep, Miró Rosa
Institut de Biotecnologia i Biomedicina, Universitat Autónoma de Barcelona, Bellaterra, Spain.
Cancer Genet Cytogenet. 2002 Aug;137(1):49-53. doi: 10.1016/s0165-4608(02)00544-7.
Comparative genomic hybridization (CGH) and conventional cytogenetic karyotyping were used to screen for losses and gains of DNA sequences along chromosomes in ten renal tumors (RCC) of different histologic types (clear-cell RCC, papillary RCC, and one oncocytoma). Loss of 3p was the most common change in clear-cell RCC. All papillary tumors, either adenomas or carcinomas revealed gains of chromosomes 7 and 17q without limitation to size and grade. Homozygotic loss of the pseudoautosomal Xp or Yp region was detected in three RCC tumors. A dicentric (Y;14) was present as the sole chromosome abnormality in the oncocytoma. Both techniques showed concordant results in tumors with homogeneous karyotype. However, in tumors with several composite clones some discrepancies were observed, especially in cases of clear-cell RCC where chromosomal abnormalities present in a low number of metaphases could not be detected by CGH.
采用比较基因组杂交(CGH)和传统细胞遗传学核型分析技术,对10例不同组织学类型(透明细胞肾细胞癌、乳头状肾细胞癌和1例嗜酸细胞瘤)的肾肿瘤(肾细胞癌)进行染色体DNA序列的缺失和增益筛查。3p缺失是透明细胞肾细胞癌最常见的改变。所有乳头状肿瘤,无论是腺瘤还是癌,均显示7号染色体和17q染色体增益,且不受大小和分级限制。在3例肾细胞癌肿瘤中检测到假常染色体Xp或Yp区域的纯合缺失。在嗜酸细胞瘤中,存在一个双着丝粒(Y;14)作为唯一的染色体异常。两种技术在核型均一的肿瘤中显示出一致的结果。然而,在具有多个复合克隆的肿瘤中,观察到一些差异,特别是在透明细胞肾细胞癌病例中,CGH无法检测到少数中期细胞中存在的染色体异常。