BACKGROUND. Six human pancreatic carcinoma cell lines, designated as KMP-1
to KMP-6, were established and maintained in vitro for > 3 years. AU were d
erived from pancreatic ductal adenocarcinomas. The six cell lines originate
d from either primary pancreatic tumors, metastatic liver tumors, or metast
ases to lymph nodes.
METHODS, Each cell line was characterized by its morphology, doubling time,
colony forming efficiency (CFE) on plastic dishes, tumorigenicity in nude
mice,chromosomal analysis, and the amount of tumor markers secreted into th
e culture medium. Furthermore, mutations in the K-ms, p53, and p16/INK4a ge
nes were analyzed.
RESULTS. All cell lines grew as an adhering monolayer and were cultured in
medium supplemented with 2% fetal bovine serum. The doubling time ranged fr
om 16-70 hours, and the CFE ranged from 0.1-11%. Subcutaneous transplantati
on of these carcinoma cells into nude mice resulted in the formation of tum
ors. Chromosomal analysis showed that the modal numbers ranged from 43-124,
and each karyotype was unique. Each cell line secreted detectable amounts
of squamous cell carcinoma antigen, carcinoembryonic antigen, carbohydrate
antigen 19-9, Dupan-II and cytokeratin 19 fragment, respectively. Genetic a
lterations of the K-rns, p53, and p16 genes were detected in six, three, an
d five, respectively, of the six cell Lines.
CONCLUSIONS. The authors believe that these newly established pancreatic ca
rcinoma cell lines will contribute to wide ranging studies regarding pancre
atic carcinoma progression. (C) 1999 American Cancer Society.