Bertrand V, Couturier-Turpin M H, Louvel A, Panis Y, Couturier D
Groupe de Recherche en Pathologie Digestive et Service d'Hépato-Gastro-Entérologie, Université René Descartes, Hôpital Cochin, Paris, France.
Cancer Genet Cytogenet. 1999 Aug;113(1):36-44. doi: 10.1016/s0165-4608(98)00194-0.
This study was aimed at elucidating the relation between the cytogenetic characteristics and the invasive ability of two human colonic adenocarcinoma cells lines, HT29 and CaCO2. These two cell lines have very different tumorigenic and metastatic capacities after intrasplenic injection into nude mice: high for HT29 and relatively weak for CaCO2. At the time of injection, cytogenetic studies of the two cell lines revealed shared abnormalities: paratriploidy with seven common extra chromosomes or chromosome regions and specific particularities. In HT29 cells, we observed a large marker of unknown origin, an isochromosome i(11)(q10) and 5, 12, 13, 15, 19, and (19q+) supernumerary chromosomes, and, finally, the absence of one chromosome 16. In CaCO2 cells, we observed a chromosome 1-derived marker with q24-31 duplication, 12q and 16 supernumerary chromosomes, and a der(16) marker. The most striking difference between the karyotypes of these two cell lines concerned chromosome 16 (under- and overexpressed in HT29 and CaCO2 cells, respectively), overexpression of chromosomes 13, 15, and 19 in HT29 cells, and the relative loss of 12p in CaCO2 cells. Although some differences may be due to the intrinsic characteristics of the stem line, the establishment of specific cytogenetic abnormalities points out the role of many regions of the genome in tumorigenic and metastatic capacities of malignant cells.
本研究旨在阐明两种人结肠腺癌细胞系HT29和CaCO2的细胞遗传学特征与侵袭能力之间的关系。将这两种细胞系经脾内注射到裸鼠体内后,它们具有非常不同的致瘤和转移能力:HT29的能力较强,而CaCO2相对较弱。在注射时,对这两种细胞系的细胞遗传学研究揭示了共同的异常情况:亚三倍体伴有7条共同的额外染色体或染色体区域以及特定的特征。在HT29细胞中,我们观察到一个来源不明的大标记物、一条等臂染色体i(11)(q10)以及5、12、13、15、19号和(19q+)额外染色体,最后还缺少一条16号染色体。在CaCO2细胞中,我们观察到一个源自1号染色体的标记物,其q24 - 31区域有重复、12号染色体和16号额外染色体以及一个der(16)标记物。这两种细胞系核型之间最显著的差异涉及16号染色体(在HT29和CaCO2细胞中分别为低表达和高表达)、HT29细胞中13、15和19号染色体的高表达以及CaCO2细胞中12p的相对缺失。尽管一些差异可能归因于干细胞系的内在特征,但特定细胞遗传学异常的出现表明基因组的许多区域在恶性细胞的致瘤和转移能力中发挥了作用。