Simon D, Munoz S J, Maddrey W C, Knowles B B
Wistar Institute of Anatomy and Biology, Thomas Jefferson University, Philadelphia, Pennsylvania 19104.
Cancer Genet Cytogenet. 1990 Apr;45(2):255-60. doi: 10.1016/0165-4608(90)90091-n.
Chromosome analysis of cells obtained at biopsy from a 65-year-old man with primary hepatocellular carcinoma revealed characteristic abnormalities of chromosomes 1, 5, 6, 9, 13, 16, and 22 in each cell and maintenance of a pseudodiploid chromosome number (46,XY). Five of the chromosomal sites involved in these rearrangements are either in fragile site regions or in regions containing genes that encode cellular oncogenes. Some of the tumor cells manifest mitotic deviations in the form of asynchronies, spiralization, premature centromere division, and non-sister chromatid associations. The significance of these findings to hepatocellular carcinogenesis is discussed.
对一名65岁原发性肝细胞癌男性患者活检获取的细胞进行染色体分析,结果显示每个细胞中1号、5号、6号、9号、13号、16号和22号染色体存在特征性异常,且维持假二倍体染色体数目(46,XY)。这些重排所涉及的染色体位点中有五个要么位于脆性位点区域,要么位于含有编码细胞癌基因的基因区域。一些肿瘤细胞表现出有丝分裂偏差,形式为不同步、螺旋化、着丝粒过早分裂和非姐妹染色单体关联。讨论了这些发现对肝细胞癌发生的意义。