Kuźniacka Alina, Mertens Fredrik, Strömbeck Bodil, Wiegant Joop, Mandahl Nils
Department of Clinical Genetics, Lund University Hospital, Lund, Sweden.
Cancer Genet Cytogenet. 2004 Jun;151(2):178-81. doi: 10.1016/j.cancergencyto.2003.09.015.
Chordoma is a rare, low- to intermediate-grade malignant tumor involving the axial spine. Cytogenetic data on these tumors have been limited to 25 cases. The findings of clonal chromosome aberrations in five new cases are presented. One of these and two previously reported cases have been studied with multicolor combined binary ratio labeling fluorescence in situ hybridization (COBRA-FISH). The karyotypes were near-diploid, mostly with several numerical and structural aberrations. There were multiple imbalances, with loss of segments from 1p, 3p, 3q, 9p, and chromosome 10 seen in two to four of the seven cases. No clustering of breakpoints was seen and no recurrent recombination between chromosomes was detected. The findings are consistent with previous data and indicate that chordoma tumor development is associated with multiple, nonrandom losses including chromosome segments that are frequently involved in many other solid tumors.
脊索瘤是一种罕见的、低至中等级别的恶性肿瘤,累及中轴脊柱。关于这些肿瘤的细胞遗传学数据仅限于25例。本文报告了5例新病例中克隆性染色体畸变的研究结果。其中1例以及之前报告的2例已采用多色组合二元比率标记荧光原位杂交(COBRA-FISH)技术进行研究。核型接近二倍体,大多伴有一些数量和结构畸变。存在多个失衡情况,在7例中的2至4例中可见1p、3p、3q、9p和10号染色体片段缺失。未观察到断点聚集现象,也未检测到染色体之间的反复重组。这些结果与先前的数据一致,表明脊索瘤的肿瘤发生与多个非随机缺失相关,包括许多其他实体瘤中常见受累的染色体片段。