Volume 18, Issue 6 pp. 1326-1333
Original Article
Free Access

Viral pathogenesis of hepatocellular carcinoma in the United States

T. Jake Liang M. D.

Corresponding Author

T. Jake Liang M. D.

Gastrointestinal Unit, Medical Services and Molecular Hepatology Laboratory, Massachusetts General Hospital Cancer Center, Massachusetts General Hospital, and Department of Medicine, Harvard Medical School, Boston, Massachusetts 02114

Gastrointestinal Unit, Jackson 812, Massachusetts General Hospital, Fruit St., Boston, MA 02114===Search for more papers by this author
Lennox J. Jeffers

Lennox J. Jeffers

Center for Liver Diseases, University of Miami School of Medicine and Veterans Affairs Medical Center, Miami, Florida 33136

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K. Rajender Reddy

K. Rajender Reddy

Center for Liver Diseases, University of Miami School of Medicine and Veterans Affairs Medical Center, Miami, Florida 33136

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Maria De Medina

Maria De Medina

Center for Liver Diseases, University of Miami School of Medicine and Veterans Affairs Medical Center, Miami, Florida 33136

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I. Talley Parker

I. Talley Parker

Center for Liver Diseases, University of Miami School of Medicine and Veterans Affairs Medical Center, Miami, Florida 33136

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Hugo Cheinquer

Hugo Cheinquer

Center for Liver Diseases, University of Miami School of Medicine and Veterans Affairs Medical Center, Miami, Florida 33136

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Victor Idrovo

Victor Idrovo

Center for Liver Diseases, University of Miami School of Medicine and Veterans Affairs Medical Center, Miami, Florida 33136

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Alfredo Rabassa

Alfredo Rabassa

Center for Liver Diseases, University of Miami School of Medicine and Veterans Affairs Medical Center, Miami, Florida 33136

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Eugene R. Schiff

Eugene R. Schiff

Center for Liver Diseases, University of Miami School of Medicine and Veterans Affairs Medical Center, Miami, Florida 33136

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First published: December 1993
Citations: 30

Abstract

Chronic hepatitis B virus infection is closely associated with the development of hepatocellular carcinoma, which is a major cause of cancer death worldwide. Recent studies have implicated hepatitis C virus infection as a major pathogenic agent of HBsAg-negative hepatocellular carcinoma. The significance of hepatitis C virus and hepatitis B virus infections in the occurrence of HBsAg-negative hepatocellular carcinoma has not been well established in the United States. We studied 91 HBsAg-negative American patients with hepatocellular carcinoma for evidence of hepatitis C virus or hepatitis B virus infection. These patients had no other predisposing factors to hepatocellular carcinoma. A sensitive polymerase chain reaction was employed to detect hepatitis C virus RNA and hepatitis B virus DNA in serum and liver. Three sets of hepatitis C virus and hepatitis B virus primers were used to optimize the detection of viral genomes. Hepatitis C virus antibodies were measured with second-generation immunoassays. Twenty-six (29%) of these patients carried low levels of hepatitis B virus DNA in either serum, liver/tumor tissue or both. On the basis of the results from serological and polymerase chain reaction analyses of serum and liver, we found that 53 of 91 patients (58%) exhibited evidence of hepatitis C virus infection. When data were combined, 14 patients (15%) had evidence of hepatitis B virus/hepatitis C virus coinfection, whereas 12 (13%) were infected with hepatitis B virus alone and 39 (43%) had hepatitis C virus only. Twenty-six (29%) had no markers of hepatitis B virus or hepatitis C virus infection. All patients with identifiable viral markers had coexisting chronic liver disease. Our study suggests that hepatitis C virus and occult hepatitis B virus infections account for most (71%) hepatocellular carcinoma cases of unknown pathogenesis in the United States. However, in some patients with hepatocellular carcinoma no defined pathogenesis is associated with development of disease. (HEPATOLOGY 1993;18:1326–1333.)

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