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[Cancer Research 50, 7843-7851, December 15, 1990]
© 1990 American Association for Cancer Research

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{alpha}-Fetoprotein in the Woodchuck Model of Hepadnavirus Infection and Disease: Normal Physiological Patterns and Responses to Woodchuck Hepatitis Virus Infection and Hepatocellular Carcinoma1

Paul J. Cote2, John L. Gerin and Bud C. Tennant

Division of Molecular Virology and Immunology, Department of Microbiology, Georgetown University Medical Center, Rockville, Maryland 20852 [P. J. C., J. L. G.], and Department of Clinical Sciences, New York State College of Veterinary Medicine, Cornell University, Ithaca, New York 14853 [B. C. T.]

Persistent infection of the eastern woodchuck (Marmota monax) with the woodchuck hepatitis virus (WHV) produces disease sequelae similar to those observed in humans with persistent hepatitis B virus infection, including hepatocellular carcinoma (HCC). To further characterize serological markers of HCC in the woodchuck, serum {alpha}-fetoprotein (AFP) was measured under normal physiological conditions and following infection with WHV. Serum AFP was elevated in association with WHV-induced hepatitis and HCC and was a useful indicator of hepatic responses in individual animals throughout the course of experimental WHV infection. The frequent occurrence of normal elevations in serum AFP during the fall and winter, however, limits the use of AFP as a marker for early detection of HCC. The present temporal studies of AFP responses in WHV-infected woodchucks have identified several stages of infection where virological and cellular interactions can be investigated at the molecular level. Studies of AFP in the woodchuck model should provide opportunities to further elucidate the physiological and immunological functions of AFP and to understand virus-host cell interactions during the course of experimental hepadnavirus infection leading to HCC.

1 This work was supported by respective Public Health Service contracts NO1-AI-72623 and NO1-AI-52585 between the National Institute of Allergy and Infectious Diseases and Georgetown and Cornell Universities.

2 To whom requests for reprints should be addressed, at Georgetown University DMVI, 5640 Fishers Lane, Rockville, MD 20852.

Received 6/22/90. Accepted 9/13/90.







HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Cancer Research Clinical Cancer Research
Cancer Epidemiology Biomarkers & Prevention Molecular Cancer Therapeutics
Molecular Cancer Research Cancer Prevention Research
Cancer Prevention Journals Portal Cancer Reviews Online
Annual Meeting Education Book Meeting Abstracts Online
Copyright © 1990 by the American Association for Cancer Research.