Human pancreatic adenocarcinoma line Capan-1 in tissue culture and the nude mouse: morphologic, biologic, and biochemical characteristics.

AP Kyriazis, AA Kyriazis, DG Scarpelli… - The American journal …, 1982 - ncbi.nlm.nih.gov
AP Kyriazis, AA Kyriazis, DG Scarpelli, J Fogh, MS Rao, R Lepera
The American journal of pathology, 1982ncbi.nlm.nih.gov
Human pancreatic ductal adenocarcinoma line Capan-1 was studied in tissue culture and
the nude mouse. In tissue culture, the neoplastic cells grew as large epithelial-like mucin-
producing cells. Subcutaneous and intraperitoneal transplantation of neoplastic cells into
nude mice resulted in tumor formation characterized by marked invasiveness and distant
metastases. Histologically, the tumor appeared as a well-differentiated mucin-producing
adenocarcinoma morphologically resembling the tumor of origin. Chromosomal analysis …
Abstract
Human pancreatic ductal adenocarcinoma line Capan-1 was studied in tissue culture and the nude mouse. In tissue culture, the neoplastic cells grew as large epithelial-like mucin-producing cells. Subcutaneous and intraperitoneal transplantation of neoplastic cells into nude mice resulted in tumor formation characterized by marked invasiveness and distant metastases. Histologically, the tumor appeared as a well-differentiated mucin-producing adenocarcinoma morphologically resembling the tumor of origin. Chromosomal analysis showed a human karyotype with a chromosome number between 51-61. Lactate dehydrogenase and beta 2-microglobulin used as tumor markers were present in both tissue culture and the serum of tumor-bearing mice. The neoplasm, which was characterized by an increased level of cAMP, had lost completely the ability to respond to secretin stimulation. The tumor grown in the nude mouse was resistant to treatment with 5-fluorouracil, behavior identical to that of the original tumor. Diphtheria toxin resulted in complete tumor destruction. Because Capan-1 tumor grown in the nude mouse shows morphologic, biologic, and biochemical characteristics similar to the tumor of origin, it may be an invaluable tool in furthering understanding of the biology of human pancreatic cancer.
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