Table 1. Influence of copy number alterations in gene deregulation in cervical cancer cell lines.
Frequency of deregulated genesa | |||||||||
CN+ | CN− | All | |||||||
Cell line | Genesb CN+ | n | EX+ | % | n | EX+ | % | EX+ | % |
CaLo | 6,864 | 4,487 | 532 | 11.9 | 16,254 | 1,686 | 10.4 | 2,218 | 10.7 |
CaSki | 7,706 | 4,912 | 728 | 14.8 | 15,829 | 2,197 | 13.9 | 2,925 | 14.1 |
HeLa | 14,276 | 8,875 | 2,207 | 24.9 | 11,866 | 3,088 | 26 | 5,295 | 25.5 |
SiHa | 17,829 | 11,120 | 1,125 | 10.1 | 9,621 | 944 | 9.8 | 2,069 | 10 |
Average | 11,669 | 7,349 | 1,148 | 15.6 | 13,393 | 1,979 | 14.8 | 3,127 | 15 |
Recurrent genese | 1,264c | 783 | 147 | 18.8 | 19,958 | 2,975 | 14.9 | 3,122d | 15.1 |
20,741 genes were explored for changes in expression with HG-ST1.0 microarray. On average 7,349 of them were CN-altered (CN+) and 13,393 did not have copy number alterations (CN−).
Potentially copy number altered genes according to data obtained with 100 k microarray. On average only 63% of those genes were explored for changes in gene expression (numbers in column n of CN+ subset).
Genes who were copy number altered in the four cell lines.
Genes who were found deregulated when all four cell lines, by triplicate, were compared together against the control sample (n = 10).
In the genome, included genes that were found in MRRs, and in the transcriptome, include genes which were found deregulated uniformly in the four cell lines (described in d).
EX+ = Genes that were up- or down- regulated in cancer cell lines compared with the control sample.