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Fas antigen (CD95) expression and apoptosis in hepatocytes of patients with chronic viral hepatitis.

AbstractBACKGROUND:
Apoptosis may be defined as programmed cell death. It is involved in the normal development and homeostasis of tissues in multicellular organisms. An increased or decreased rate of apoptosis may lead to a range of diseases. Fas antigen is a cell-surface receptor that induces apoptotic pathways when treated with Fas ligand or anti-Fas antibody. There is increasing evidence that apoptosis plays an important role in the immunopathogenesis of chronic viral hepatitis, in which the Fas antigen-Fas ligand pathway is particularly involved.
METHODS:
Fas antigen expression and apoptosis (apoptotic index) were assayed using flow cytometry in the hepatocytes of 27 patients with chronic viral hepatitis. Histopathological activity, scored by Knodell's histological activity index, other histopathological parameters, serum transaminase values and patient age were then compared with apoptotic index and Fas antigen expression.
RESULTS:
Apoptosis and Fas antigen expression in hepatocytes were correlated closely with histological activity (grade) of chronic viral hepatitis, but there were no correlations with histological stage, patient age or serum transaminase levels.
CONCLUSION:
Apoptosis and its triggering molecule, Fas antigen, induce mechanisms that appear to be associated with the pathogenesis of chronic viral hepatitis.
AuthorsMurat Kiyici, Selim Gurel, Ferah Budak, Enver Dolar, Macit Gulten, Selim Giray Nak, Faruk Memik
JournalEuropean journal of gastroenterology & hepatology (Eur J Gastroenterol Hepatol) Vol. 15 Issue 10 Pg. 1079-84 (Oct 2003) ISSN: 0954-691X [Print] England
PMID14501615 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • fas Receptor
  • Transaminases
Topics
  • Adolescent
  • Adult
  • Apoptosis
  • DNA Fragmentation
  • Female
  • Flow Cytometry
  • Hepatitis B, Chronic (metabolism, pathology)
  • Hepatitis C, Chronic (metabolism, pathology)
  • Hepatocytes (metabolism, physiology)
  • Humans
  • Male
  • Middle Aged
  • Transaminases (blood)
  • fas Receptor (metabolism)

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