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
. 1986 Oct;83(20):7780-4.
doi: 10.1073/pnas.83.20.7780.

Identification of a pituitary factor responsible for enhancement of plasminogen activator activity in breast tumor cells

Identification of a pituitary factor responsible for enhancement of plasminogen activator activity in breast tumor cells

R Mira-y-Lopez et al. Proc Natl Acad Sci U S A. 1986 Oct.

Abstract

Sheep pituitary glands contain a protein that stimulates plasminogen activator (PA) activity 3- to 20-fold in serum-free cultures of T47D, MTW9/PL, and SC115 breast tumor cells. This protein was found to be similar to basic fibroblast growth factor (bFGF) in size, cationic nature, and affinity for heparin. Purified human placental bFGF, a homologue of human and bovine pituitary bFGF, was effective in stimulating mammary tumor cell PA at a concentration of 1 ng/ml. Antibodies to placental bFGF blocked the PA stimulatory activity of sheep pituitary extracts. Because of these properties, the active protein in sheep pituitary glands was identified as bFGF. This represents another function of bFGF, indicating that its spectrum of target cells is wider than previously thought. Because of previously established correlations between PA production in vitro and tumor growth in vivo, we suggest that bFGF may contribute to the growth of breast carcinomas in vivo. Other types of carcinomas may also be affected by bFGF.

PubMed Disclaimer

References

    1. J Biol Chem. 1975 Apr 10;250(7):2515-20 - PubMed
    1. Am J Surg. 1960 Apr;99:544-52 - PubMed
    1. Anal Biochem. 1976 May 7;72:248-54 - PubMed
    1. Cell. 1976 Feb;7(2):223-6 - PubMed
    1. Clin Oncol. 1976 Jun;2(2):121-6 - PubMed

Publication types