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
. 1995 May;13(3):191-5.
doi: 10.1007/BF00132207.

Expression of antisense epidermal growth factor receptor RNA downmodulates the malignant behavior of human colon cancer cells

Affiliations

Expression of antisense epidermal growth factor receptor RNA downmodulates the malignant behavior of human colon cancer cells

S Chakrabarty et al. Clin Exp Metastasis. 1995 May.

Abstract

Human colon cancer (Moser) cells produce and secrete epidermal growth factor (EGF) and respond to EGF via an autocrine/paracrine mode through the cell surface EGF receptor (EGFR). In this report we show that EGF promotes the malignant behavior of the Moser cells in vitro in terms of growth in soft agarose and invasion of Matrigel-coated porous membranes. Expressing antisense EGFR RNA in the Moser cells (through transfection with an inducible antisense EGFR expression vector) downmodulated the expression of cell surface EGFR and EGFR mRNA with a concurrent inhibition of growth in soft agarose and invasion of Matrigel-coated membranes. In addition, the ability of exogenously applied EGF in promoting the malignant behavior of these cells was circumvented. We conclude that antisense EGFR RNA was a potent agent in circumventing the in vitro malignant properties of the Moser cells.

PubMed Disclaimer

Similar articles

Cited by

References

    1. Cancer Metastasis Rev. 1984;3(3):177-91 - PubMed
    1. Cell. 1991 Jan 25;64(2):271-80 - PubMed
    1. Int J Cancer Suppl. 1994;8:103-7 - PubMed
    1. J Cell Physiol. 1991 Aug;148(2):220-7 - PubMed
    1. Cell. 1984 Feb;36(2):371-9 - PubMed

Publication types

MeSH terms

LinkOut - more resources