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
. 1991 May;36(5):653-8.
doi: 10.1007/BF01297034.

Protooncogenes and growth factors associated with normal and abnormal liver growth

Affiliations
Review

Protooncogenes and growth factors associated with normal and abnormal liver growth

N Fausto. Dig Dis Sci. 1991 May.

Abstract

Hepatocyte replication during liver regeneration depends on extrinsic (circulating) and intrinsic (intrahepatic) factors. Two important growth factors produced in the regenerating liver are discussed, TGF alpha, an autocrine, stimulatory growth factor, and TGF beta, a paracrine inhibitory factor. The balance between the activities of these factors is likely to play an important role in regulating hepatocyte proliferation. The expression of some protooncogenes occurs sequentially during the first few hours after partial hepatectomy and is a marker for the entry of hepatocytes into the cell cycle (proliferative competence). As hepatocytes become competent to proliferate, they respond to TGF alpha and other growth factors and enter a proliferative phase. It is possible that TGF beta 1 serves as a stop signal for liver regeneration but the mechanisms by which TGF beta inhibits hepatocyte DNA synthesis are still unknown.

PubMed Disclaimer

Similar articles

Cited by

References

    1. Cancer Res. 1986 Mar;46(3):1015-29 - PubMed
    1. Lab Invest. 1989 Jan;60(1):4-13 - PubMed
    1. Cell Growth Differ. 1990 Mar;1(3):103-11 - PubMed
    1. Biochem Biophys Res Commun. 1989 Sep 15;163(2):967-73 - PubMed
    1. Science. 1989 Mar 31;243(4899):1689-94 - PubMed

Publication types

MeSH terms

Substances

LinkOut - more resources