Jw. Kim et al., ESTABLISHMENT AND CHARACTERIZATION OF A CELL-LINE (CUMC-3) DERIVED FROM A HUMAN SQUAMOUS CARCINOMA OF THE UTERINE CERVIX, Gynecologic oncology, 57(1), 1995, pp. 47-60
A new cell line, CUMC-3, has been derived from an invasive nonkeratini
zing squamous cell carcinoma of the uterine cervix in a 32-year-old pa
tient. It has been maintained in long-term culture for 59 months, and
passaged over 310 times. Monolayer-cultured cells were polygonal in sh
ape, showing a pavement-like arrangement and a tendency to pile up wit
hout contact inhibition. The epithelial nature of the cultured CUMC-3
cells was also confirmed by transmission electron microscopy which dem
onstrated the presence of desmosomes and tonofilaments. The cells were
highly tumorigenic in nude mice and the transplanted tumors were poor
ly differentiated squamous carcinoma which closely resembled the origi
nal tumor. Cultured cells obtained from the CUMC-3-derived nude mouse
tumor, CUMC-3N, also were studied for its characterization. Repeated c
hromosome analysis revealed a stable clone with the modal chromosome n
umber of 78. The metaphase of this cell line had multiple structural a
berrations of chromosomes 1, 3, 8, 10, 11, 20, and X and showed severa
l markers of unknown origin. The results of isozyme analyses were dist
inct from the HeLa cell line, The identical genetic signature was demo
nstrated both in CUMC-3 and in CUMC-3N cells. Cultured CUMC-3 cells pr
oduced human chorionic gonadotropin P-subunit and tumor antigen of squ
amous cell carcinoma (TA-4). Cytosol estrogen receptors were found in
this cell line but progesterone receptors were not measured, HLA typin
g of CUMC-3 cells indicated the presence of DR4, DR8, DQw3, and DQw6.
The result of oncogene analysis using Southern blotting technique reve
aled no amplification of oncogene c-myc. Analysis of the DNA samples e
xtracted from the CUMC-3 cells showed the presence of human papillomav
irus type 16 DNA. Using the single-strand conformation polymorphism te
chnique, we have screened CUMC-3 cells for p53 mutation in exons 4 to
9. No mobility shift was observed in this cell line. This cell line ma
y be useful in studying the in vitro and in vivo properties of human c
ervical carcinoma. (C) 1995 Academic Press, Inc.