S. Endo et al., NONRANDOM KARYOTYPIC CHANGES IN A SPONTANEOUSLY IMMORTALIZED AND TUMORIGENIC SYRIAN-HAMSTER EMBRYO CELL-LINE, Carcinogenesis, 15(10), 1994, pp. 2387-2390
Syrian hamster embryo (SHE) cells were used as a model system to study
genetic changes during the rare spontaneous progression from normal t
o immortalized and then to neoplastically transformed cells. Cultures
were established for immortalized and/or neoplastically transformed ce
lls by inoculating 2-5 x 10(5) primary cells into 75 cm(2) culture fla
sks and subsequent subculture at subconfluence. We examined the karyot
ypic changes in the spontaneously transformed and tumourigenic SHE cel
ls. Chromosome analyses were performed on mitotic cells with the quina
crine banding technique. The primary SHE cell stock (82-6) was karyoty
pically normal, but cells that had overcome senescence exhibited chrom
osome abnormalities. More than 90% of cells from passages 18-85 carrie
d the same deletion in the short arm of chromosome 2 (2p-). This delet
ion was also found in about 70% of cells analysed at passage 15. 2p- w
as never found in cells at passage 4. We further observed a variety of
numeric and structural chromosome changes in addition to 2p-, but the
se were seen only in transformed cells at high passage numbers and in
cell lines derived from nude mice tumours. Our findings suggest that 2
p- predisposed SHE cells either to immortalization and/or to progressi
on to tumourigenicity.