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
. 2009 Apr;454(4):369-79.
doi: 10.1007/s00428-009-0753-7. Epub 2009 Mar 12.

Hedgehog signaling is involved in differentiation of normal colonic tissue rather than in tumor proliferation

Affiliations

Hedgehog signaling is involved in differentiation of normal colonic tissue rather than in tumor proliferation

Beate Alinger et al. Virchows Arch. 2009 Apr.

Abstract

The Hedgehog (Hh) pathway is a main regulation cascade in embryonic differentiation. It is also present in adult tissues and unusual expression has been associated with formation of benign and malignant lesions. We examined the presence of the Hedgehog pathway in normal and pathological human colon tissue. Components investigated include Sonic (Shh), Indian (Ihh), and Desert Hedgehog (Dhh), Gli1, Gli2, Gli3, and Patched (Ptch). Pathological tissue samples comprised 23 benign and 20 malignant lesions of human colon. The influence of the Hedgehog pathway on differentiation and proliferation has been investigated by analyzing the effect of the pathway inhibitor Cyclopamine on human colon cancer cell lines HT29 and CaCo2. In normal colon, we detected expression of Shh and Dhh within the lining epithelium and Patched, Gli1, and Gli2 along the whole crypts. Within all benign lesions, positive staining of Shh, Dhh, Gli1, Gli2, and Ptch was detected. Expression of Shh and Dhh was restricted to single cell aggregates. Malignant lesions also displayed focal staining pattern for Shh and Dhh but to a much lesser extent. We conclude that Hedgehog signaling is involved rather in constant differentiation and renewing of the colonic lining epithelium than in cancer formation, growth, or proliferation.

PubMed Disclaimer

References

    1. Cell. 1996 Oct 18;87(2):159-70 - PubMed
    1. Am J Med Genet A. 2003 Nov 15;123A(1):5-28 - PubMed
    1. Nature. 2003 Oct 23;425(6960):846-51 - PubMed
    1. Gastroenterology. 2001 Aug;121(2):485-7 - PubMed
    1. J Immunol Methods. 1983 Dec 16;65(1-2):55-63 - PubMed

Publication types

MeSH terms

LinkOut - more resources