Comparison of features of human lung cancer cell lines and their corresponding tumors

Citation
Ii. Wistuba et al., Comparison of features of human lung cancer cell lines and their corresponding tumors, CLIN CANC R, 5(5), 1999, pp. 991-1000
Citations number
32
Categorie Soggetti
Oncology
Journal title
CLINICAL CANCER RESEARCH
ISSN journal
10780432 → ACNP
Volume
5
Issue
5
Year of publication
1999
Pages
991 - 1000
Database
ISI
SICI code
1078-0432(199905)5:5<991:COFOHL>2.0.ZU;2-X
Abstract
Although human lung tumor-derived cell lines play an important role in the investigation of lung cancer biology and genetics, there is no comprehensiv e study comparing the genotypic and phenotypic properties of lung cancer ce ll lines with those of the individual tumors from which they were derived, We compared a variety of properties of 12 human non-small cell lung carcino ma (NSCLC) cell lines (cultured for a median period of 39 months; range, 12 -69) and their corresponding archival tumor tissues. There was, in general, an excellent concordance between the lung tumor cell lines and their corre sponding tumor tissues for morphology (100%), the presence of aneuploidy (1 00%), immunohistochemical expression of HER2/neu (100%) and p53 proteins (1 00%), loss of heterozygosity at 13 chromosomal regions analyzed (97%) using 37 microsatellite markers, microsatellite alterations (MAs, 75%), TP53 (67 %), and K-ras (100%) gene mutations, In addition, there was 100% concordanc e for the parental allele lost in all 115 comparisons of allelic losses. So me discrepancies were found; more aneuploid subpopulations of cells were de tected in the cell lines as well as higher incidences of TP53 mutations (4 of 10 mutations not found in the tumors) and microsatellite alterations (tw o cell lines with MAs not detected in the tumors). Similar loss of heterozy gosity frequencies by chromosomal regions and mean fractional allelic loss index were detected between successfully cultured and 40 uncultured lung tu mors (0.45 and 0.49, respectively), indicating that both groups were simila r. Our findings indicate that the NSCLC cell lines in the large majority of instances retain the properties of their parental tumors for lengthy cultu re periods. NSCLC cell lines appear very representative of the lung cancer tumor from which they were derived and thus provide suitable model systems for biomedical studies of this important neoplasm.