Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 1991;117(5):416-20.
doi: 10.1007/BF01612760.

Effects of insulin and somatostatin on the growth and the colony formation of two human pancreatic cancer cell lines

Affiliations

Effects of insulin and somatostatin on the growth and the colony formation of two human pancreatic cancer cell lines

Y Takeda et al. J Cancer Res Clin Oncol. 1991.

Abstract

The effects of insulin and somatostatin on the growth and the colony formation of two human pancreatic cancer cell lines, BxPC-3 and SOJ-6, were studied. The BxPC-3 cell line (American Type Culture Collection no. CRL 1687) was derived from a moderately differentiated pancreatic adenocarcinoma. The SOJ-6 cell line is a subclone of SOJ that was initiated from ascites of a well-differentiated pancreatic adenocarcinoma. Both cell lines express fetoacinar pancreatic antigen, an antigen that might be associated with early transformation stages. However, these lines have different proliferation and tumoral powers. SOJ-6 cells showed an almost twofold higher division rate over BxPC-3 cells when cultured in RPMI-1640 medium containing 10% fetal bovine serum. The tumorigenic degree of SOJ-6 cells, as assessed by tumor growth in nude mice, was about three times greater than that of BxPC-3. The in vitro growth of BxPC-3 cells was significantly promoted by insulin, and was slightly inhibited by somatostatin, whereas the growth of SOJ-6 cells was not influenced by these hormones. Using a clonogenic assay in soft agar, the average ratio of colony numbers formed by SOJ-6 and BxPC-3 was about 10/1, indicating a good correlation between the colony formation and tumorigenic degree in vivo. In this test, the number of colonies formed by BxPC-3 cells was increased about twofold in insulin-supplemented medium. On the other hand, somatostatin inhibited the colony formation by a factor of four to six. However, no hormonal modulation of the colony formation of SOJ-6 cells was observed. Our data show that pancreatic cancer cell lines respond differently to pancreatic hormones, and suggest that this may be correlated to a tumour stage or a tumour type.

PubMed Disclaimer

References

    1. Albers GHR, Escribano MJ, Daher N, Nap M (1990) FAP protein in the normal pancreas, chronic pancreatitis, pancreatic adenocarcinoma and intraabdominal metastasis of adenocarcinomas. An immunological study. Am J Clin Pathol 93:14–20 - PubMed
    1. Bockman DE (1981) Cells of origin of pancreatic cancer: experimental animal tumors related to human pancreas. Cancer 47:1528–1534 - PubMed
    1. Carre-Llopis A, Loridon-Rosa B, Escribano M (1987) Ultrastructual changes in acinar cells of hamster pancreas in chemically induced carcinogenesis. Cell Biol Int Rep 11:no.9 - PubMed
    1. Eriguchi M, Carre-Llopis A, Orbach-Arbouys S, Escribano MJ (1987) Evolution of expression of fetal acinar antigens during carcinogenesis of the pancreas of hamster: individual follow-up by open biopsy. JNCI 78:519–525 - PubMed
    1. Escribano MJ, Carre-Llopis A, Loridon-Rosa B (1985) Expression of oncofetal pancreatic antigens in hamster adult pancreas during experimental carcinogenesis. Br J Cancer 51:187–193 - PMC - PubMed

Publication types

LinkOut - more resources