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.