Table 2.
Chromosome number | |||||||
---|---|---|---|---|---|---|---|
1- | 4- | 7- | 9- | 12q | 14- | X- | |
Control | <1 | 6.0 ± 3.0 | <1.0 | 6.0 ± 3.0 | <1.0 | <1.0 | <1.0 |
Tumors | 80.0 ± 26 | 98.0 ± 3 | 86.0 ± 10 | 75.0 ± 13 | 86.0 ± 7 | 72.0 ± 8 | 98.0 ± 20 |
Eleven hepatocellular carcinomas isolated from the c-myc/TGF-α mice and hepatocytes from five age-matched (Cd 1 × B6CBA)F1 mice were cultured as described in Materials and Methods, and metaphase preparations were made from the first two divisions. The metaphase spreads from 11 tumors and hepatocytes from five age-matched controls were hybridized with chromosomal paints for chromosomes 1, 4, 5, 7, 8, 9, 11, and 12 and the X chromosome. At least 20 metaphase spreads were analyzed for each chromosome paint. The inverted DAPI from each hybridized metaphase spread was analyzed to determine the band region that was altered. A minimum of 20 G-banded metaphase spreads were karyotyped for each tumor and control. The data are expressed as the mean percent ± SD of cells with a specific aberration.