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 Jan;53(1):29-35.
doi: 10.1038/bjc.1986.5.

Indirect mechanism of oestradiol stimulation of cell proliferation of human breast cancer cell lines

Free PMC article

Indirect mechanism of oestradiol stimulation of cell proliferation of human breast cancer cell lines

A E Lykkesfeldt et al. Br J Cancer. 1986 Jan.
Free PMC article

Abstract

The human breast cancer cell line MCF-7 requires oestrogen to produce and promote growth of tumours in athymic mice. In vitro, however, MCF-7 cells proliferate rapidly without supply of oestrogen (Briand & Lykkesfeldt, 1984). Oestrogen stimulation of proliferation of MCF-7 cells can be achieved when the cells are grown at high concentration of newborn calf serum (NCS, 10%) or oestrogen deprived foetal calf serum (10%). The stimulation involves an abolishment of inhibitory activity present in the serum. The oestradiol stimulated cultures grow rapidly for a much longer time period and attain a much higher cell density than the unstimulated cultures. Oestrogen is specific for the promotion of cell proliferation and only oestrogen receptor positive cell lines with a functional oestrogen receptor mechanism can be stimulated. We assume that oestradiol acts directly on the cells and via the oestrogen receptor mechanism induces the synthesis of a substance which abolishes the inhibitory activity in serum. We call this mechanism of action an indirect stimulation of cell proliferation. A similar mechanism may exist in vivo since we find that serum from athymic mice contains a growth inhibitory activity towards MCF-7 cells and the inhibitory effect can be abolished by oestradiol.

PubMed Disclaimer

Similar articles

Cited by

References

    1. Cancer Res. 1976 Dec;36(12):4595-601 - PubMed
    1. Biochem Biophys Res Commun. 1984 Aug 16;122(3):1097-103 - PubMed
    1. Nature. 1979 Oct 4;281(5730):388-9 - PubMed
    1. Science. 1980 Aug 8;209(4457):701-2 - PubMed
    1. Eur J Cancer. 1980 Aug;16(8):1007-15 - PubMed

Publication types