Pandis N, Bardi G, Sfikas K, Panayotopoulos N, Tserkezoglou A, Fotiou S
Department of Cellular Physiology, Papanikolaou Research Center, Hellenic Anticancer Institute, Athens, Greece.
Cancer Genet Cytogenet. 1990 Oct 1;49(1):51-6. doi: 10.1016/0165-4608(90)90163-5.
Cytogenetic analysis of short-term cultures from 10 uterine leiomyomas revealed normal karyotypes in 8 and clonal complex chromosome rearrangements in 2 tumors. In both leiomyomas with clonal abnormalities, 12q14, but not 14q22-24, was involved in translocations with 1q43 in one tumor and with 12q24 in the other. Additional chromosome abnormalities were found in both cases: 1-5 rings and monosomy of chromosome 9 in case 1, and complex numerical and structural abnormalities of chromosomes 1, 6-8, 11, 13, 16, 17, and 22 in case 2. The consistent cytogenetic rearrangement of 12q14 in uterine leiomyomas, sometimes without concomitant 14q changes, indicates that a gene of critical importance for leiomyoma development may be found in this band.
对10个子宫平滑肌瘤的短期培养物进行细胞遗传学分析,结果显示8个核型正常,2个肿瘤存在克隆性复杂染色体重排。在这两个具有克隆异常的平滑肌瘤中,一个肿瘤中12q14与1q43发生易位,另一个肿瘤中12q14与12q24发生易位,但14q22 - 24未参与。两例均发现其他染色体异常:病例1有1 - 5个环状染色体和9号染色体单体,病例2有1、6 - 8、11、13、16、17和22号染色体复杂的数目和结构异常。子宫平滑肌瘤中12q14一致的细胞遗传学重排,有时无伴随的14q改变,表明该区域可能存在对平滑肌瘤发生至关重要的基因。