A. Gaspericampani et al., MOLECULAR AND BIOLOGICAL FEATURES OF 2 NEW HUMAN SQUAMOUS AND ADENOCARCINOMA OF THE LUNG-CELL LINES, Cancer genetics and cytogenetics, 107(1), 1998, pp. 11-20
Two human cancer cell lines were established from metastatic lesions o
f an adenocarcinoma (RAL) and a squamous cell (CAEP) carcinoma of the
lung. The clinical histories of the patients from whom the cell lines
were derived are reported. The lines were maintained in continuous cul
ture with doubling times of 65 (RAL) and 50 (CAEP) hours. The RAL and
CAEP cell lines, whose morphology and ultrastructural features are pre
sented, showed extensively rearranged karyotypes with modal number of
85 (RAL) and 98 (CAEP). In particular, chromosome 2 pentasomy and seve
ral clonal markers rr ere evident in the RAL cells, whereas a telomeri
c deletion of chromosome 1, del (1)(q32), was observed in the CAEP cel
ls. The morphologic data were confirmed bq high expression of specific
antigens for each histotype. A marked positivity of the neuron-specif
ic enolase (NSE) levels was evident by immunoenzymatic assays in the c
ell lines cytosol with respect to those present in the respective pati
ent's sera. No amplification or rearrangements were evident in the CMY
C, LMYC, NMYC, INT-2, ERBB2, HRAS, KRAS, MOS, HST-1 genes by Southern
blotting analysis in each cell line. Point mutations in exon 1 of I;RA
S and in exon 7 of TP53 were evident by polymerase chain reaction (PCR
)-DNA sequencing in the RAL cell line, whereas no alterations were pre
sent in the HRAS and RE genes. The four genes studied did not show poi
nt mutations in the CAEP cell line. The RAL cell line was resistant to
all the drugs tested, whereas the CAEP cells were sensitive to vinbla
stine. These cell lines may represent useful experimental models to in
vestigate lung cancer biology and anticancer drug response. (C) Elsevi
er Science Inc., 1998.