Over expression of transforming growth factor-alpha and epidermal growth factor receptor in human hepatic cirrhosis tissues

Hepatogastroenterology. 2008 Jan-Feb;55(81):169-72.

Abstract

Background/aims: Transforming growth factor-alpha has 30% amino acid homology to epidermal growth factor and binds with the same membrane-bound receptor, epidermal growth factor receptor. The purpose of this study was to investigate the expression of transforming growth factor-alpha and epidermal growth factor receptor in human hepatic cirrhosis tissues.

Methodology: Expression of transforming growth factor-alpha and epidermal growth factor receptor was evaluated by immunohistochemistry stain in sixty-three hepatic cirrhosis specimens and five normal liver specimens.

Results: The transforming growth factor-alpha and epidermal growth factor receptor expression rates were 84.1% (53/63) and 52.4% (33/63), respectively. These positive granules were brown and most common in cytoplasm or cell membrane of hepatocytes. There was prominently positive correlation between transforming growth factor-alpha and epidermal growth factor receptor (P<0.05, gamma=0.32). In five normal liver tissues, transforming growth factor-alpha and epidermal growth factor receptor were not detectable in hepatocytes and bile ducts.

Conclusions: Hepatic cirrhosis might be under the autocrine regulation of transforming growth factor-alpha and its receptor, epidermal growth factor receptor. Increasing expression of transforming growth factor-alpha and epidermal growth factor receptor might be one of the important events in hepatic cirrhosis pathogenesis. Furthermore, transforming growth factor-alpha might play a role in morphogenesis and regeneration of intrahepatic bile ducts.

MeSH terms

  • Bile Ducts, Intrahepatic / metabolism
  • Cytoplasm / metabolism
  • ErbB Receptors / metabolism*
  • Female
  • Gene Expression Regulation / physiology*
  • Humans
  • Immunohistochemistry
  • Liver / metabolism*
  • Liver Cirrhosis / metabolism*
  • Male
  • Transforming Growth Factor alpha / metabolism*

Substances

  • Transforming Growth Factor alpha
  • ErbB Receptors