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
Review
. 2003 Oct;8(4):395-408.
doi: 10.1023/B:JOMG.0000017427.14751.8c.

Integrin signaling and mammary cell function

Affiliations
Review

Integrin signaling and mammary cell function

Franziska Schatzmann et al. J Mammary Gland Biol Neoplasia. 2003 Oct.

Abstract

The mammary gland is a highly organized tissue, containing ductal structures, secretory alveolar units, and a supporting stroma. The organization of the epithelial cells within the tissue depends upon cell-cell adhesion as well as cell interactions with the extracellular matrix that underlies the epithelial units and makes up most of the organization of the stroma. Adhesion to the extracellular matrix is mediated by a class of heterodimeric transmembrane receptors called integrins, which cluster at focal adhesions. Integrins link the matrix with an intracellular structural scaffold, the cytoskeleton, as well as with signaling enzymes that direct cell survival, proliferation, differentiation, and migration. Two key enzymes that are recruited to sites of integrin clustering are focal adhesion kinase and integrin-linked kinase. Both enzymes are involved with communication downstream of integrins and have key roles in regulating cell behavior. This review will focus on what is known about focal adhesion kinase and integrin-linked kinase signaling and will discuss current evidence about their role in mammary gland biology and neoplasia.

PubMed Disclaimer

Similar articles

Cited by

References

    1. Prog Biophys Mol Biol. 1999;71(3-4):435-78 - PubMed
    1. Mol Cell Biol. 1999 Sep;19(9):6120-9 - PubMed
    1. Lancet. 1993 Oct 23;342(8878):1024-5 - PubMed
    1. J Cell Biol. 2001 Apr 30;153(3):585-98 - PubMed
    1. Mol Biol Cell. 2002 Oct;13(10):3521-31 - PubMed

Publication types

MeSH terms

LinkOut - more resources