König J J, Kamst E, Hagemeijer A, Romijn J C, Horoszewicz J, Schröder F H
Department of Urology, Erasmus University, Rotterdam, The Netherlands.
Urol Res. 1989;17(2):79-86. doi: 10.1007/BF00262025.
The cytogenetic evolution of the prostatic adenocarcinoma cell line LNCaP was investigated during long term in vitro culture. Study of five different sublines demonstrated that the original karyotype was well preserved in all sublines, with respect to the chromosome number as well as to the primary markers. All sublines showed additional, subline specific secondary marker chromosomes. Comparison of these markers in androgen responsive and nonresponsive sublines showed rearrangement of the short arm of chromosome 8 in both unresponsive sublines. The breakpoints were in 8p21 and 8p23, respectively, resulting in deletion of the 8p23----pter region in both sublines. In contrast, the hormone responsive sublines did not show any aberrations in chromosome 8. Review of published karyotypes of patients and cell lines seems to support our finding of partial deletion of 8p in androgen unresponsive prostate tumor cells.
在长期体外培养过程中,对前列腺腺癌细胞系LNCaP的细胞遗传学进化进行了研究。对五个不同亚系的研究表明,就染色体数目以及主要标记而言,所有亚系中原始核型均保存良好。所有亚系均显示出额外的、亚系特异性的次要标记染色体。对雄激素反应性和无反应性亚系中这些标记的比较表明,两个无反应性亚系中均出现了8号染色体短臂的重排。断点分别位于8p21和8p23,导致两个亚系中8p23----pter区域缺失。相比之下,激素反应性亚系在8号染色体上未显示任何畸变。对已发表的患者和细胞系核型的回顾似乎支持了我们关于雄激素无反应性前列腺肿瘤细胞中8p部分缺失的发现。