Relation between cytogenetic characteristics of two human colonic adenocarcinoma cell lines and their ability to grow locally or metastasize or both:An experimental study in the nude mouse

Citation
V. Bertrand et al., Relation between cytogenetic characteristics of two human colonic adenocarcinoma cell lines and their ability to grow locally or metastasize or both:An experimental study in the nude mouse, CANC GENET, 113(1), 1999, pp. 36-44
Citations number
27
Categorie Soggetti
Onconogenesis & Cancer Research
Journal title
CANCER GENETICS AND CYTOGENETICS
ISSN journal
01654608 → ACNP
Volume
113
Issue
1
Year of publication
1999
Pages
36 - 44
Database
ISI
SICI code
0165-4608(199908)113:1<36:RBCCOT>2.0.ZU;2-6
Abstract
This study was aimed at elucidating the relation between the cytogenetic ch aracteristics and the invasive ability of two human colonic adenocarcinoma cell lines, HT29 and Caco2. These two cell lines have very different tumori genic and metastatic capacities after intrasplenic injection into nude mice : high for HT29 and relatively weak for Caco2. At the time of injection, cy togenetic studies of the two cell lines revealed shared abnormalities: para triploidy with seven common extra chromosomes or chromosome regions and spe cific 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(+)) su pernumerary chromosomes, and, finally, the absence of one chromosome 16. In Caco2 cells, we observed a chromosome I-derived marker with q24-31 duplica tion, 12q and 16 supernumerary chromosomes, and a der(16) marker. The most striking difference between the karyotypes of these two cell lines concerne d chromosome 16 (under- and overexpressed in HT29 and Caco2 cells, respecti vely), 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 t o the intrinsic characteristics of the stem line, the establishment of spec ific cytogenetic abnormalities points out the role of many regions of the g enome in tumorigenic and metastatic capacities of malignant cells. (C) Else vier Science Inc., 1999.