Hagemeijer A, Versnel M A, Van Drunen E, Moret M, Bouts M J, van der Kwast T H, Hoogsteden H C
Department of Cell Biology, Erasmus University, Rotterdam, The Netherlands.
Cancer Genet Cytogenet. 1990 Jul 1;47(1):1-28. doi: 10.1016/0165-4608(90)90258-c.
Cytogenetic analyses of 40 confirmed malignant mesotheliomas (MMs) are reported. Pleural effusion cells were studied in 90% of the cases by direct method or after culture or both. Biopsy and ascites fluid were also analyzed in some patients. A normal karyotype was found in nine cases, and complex karyotypic abnormalities were observed in 30 cases. In one case, analyzable metaphases were not obtained. The chromosomal changes were all complex and heterogeneous; no consistent presumably specific abnormality was detected. Nevertheless, two main patterns of nonrandom abnormalities were observed: 1) loss of chromosomes 4 and 22, 9p, and 3p in the most of the abnormal cases and corresponding to a hypodiploid and/or hypotetraploid modal chromosome number; and 2) gain of chromosomes 7, 5, and 20 with deletion or rearrangement of 3p as well in the hyperdiploid cases, which were a minority in our series. These findings are discussed in view of other reported cytogenetic studies of MM, asbestos exposure, and possible mechanisms of malignant transformation.
本文报告了40例确诊恶性间皮瘤(MM)的细胞遗传学分析结果。90%的病例通过直接法、培养法或两种方法结合对胸腔积液细胞进行了研究。部分患者还对活检组织和腹水进行了分析。9例病例核型正常,30例观察到复杂的核型异常。1例未获得可分析的中期分裂相。染色体变化均复杂且异质性强;未检测到一致的、可能具有特异性的异常。然而,观察到两种主要的非随机异常模式:1)大多数异常病例中4号和22号染色体、9p和3p缺失,对应亚二倍体和/或亚四倍体的众数染色体数;2)超二倍体病例中7号、5号和20号染色体增加,同时伴有3p缺失或重排,此类病例在本研究系列中占少数。结合其他已报道的MM细胞遗传学研究、石棉暴露情况以及恶性转化的可能机制对这些发现进行了讨论。