Volume 20, Issue 5 pp. 1109-1114
Original Article
Free Access

Expression of the c-myc protooncogene product in cells infected with the hepatitis delta virus

Gianfranco Tappero

Gianfranco Tappero

Clinica Medica Generale, University of Turin Medical School, 10043 Orbassano

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Gioacchino Natoli

Gioacchino Natoli

I Clinica Medica, University “La Sapienza,” 00100 Rome, Ospedale Molinette, 10126 Turin, Italy

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Giovanni Anfossi

Giovanni Anfossi

Department of Clinical and Biological Sciences, University of Turin Medical School, 10043 Orbassano

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Floriano Rosina

Floriano Rosina

Department of Gastroenterology, Ospedale Molinette, 10126 Turin, Italy

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Francesco Negro

Francesco Negro

Department of Gastroenterology, Ospedale Molinette, 10126 Turin, Italy

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Antonina Smedile

Antonina Smedile

Department of Gastroenterology, Ospedale Molinette, 10126 Turin, Italy

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Ferruccio Bonino

Ferruccio Bonino

Department of Gastroenterology, Ospedale Molinette, 10126 Turin, Italy

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Alberto Angeli

Alberto Angeli

Clinica Medica Generale, University of Turin Medical School, 10043 Orbassano

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Robert H. Purcell

Robert H. Purcell

Hepatitis Virus Section, Laboratory of Infectious Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland 20892

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Professor Mario Rizzetto M.D.

Corresponding Author

Professor Mario Rizzetto M.D.

Department of Gastroenterology, Ospedale Molinette, 10126 Turin, Italy

Department of Gastroenterology, Ospedale Molinette, Corso Bramante 88, 10126 Turin, Italy===Search for more papers by this author
Massimo Levrero

Massimo Levrero

I Clinica Medica, University “La Sapienza,” 00100 Rome, Ospedale Molinette, 10126 Turin, Italy

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First published: November 1994

Abstract

The intrahepatic accumulation of the c-myc protooncogene product was observed on immunoflourescence in each of six patients with chronic hepatitis delta virus infection who exhibited the hepatitis D antigen in their livers. The c-myc product was stained in the same nuclei that contained the hepatitis D antigen. C-myc was not observed in acute hepatitis D or in cases of chronic hepatitis delta virus infection without expression of the hepatitis D antigen. The protooncogene product was detected in only 1 of 32 viral and nonviral liver disorders unrelated to hepatitis delta virus. To confirm these observations, we transfected HBsAg-positive (PCL/PRF/5) and HBsAg-negative (HepG2) transformed liver cell lines with a plasmid containing a hepatitis delta virus cDNA trimer under the control of the SV40 early enhancer/promoter sequences. Whereas baseline c-myc expression was barely detectable in mock-transfected PLC/PRF/5 or HepG2 cells, strong c-myc nuclear fluorescence was observed when these same cells were transfected with the hepatitis D antigen expression vector. Similar results were obtained after infection of HeLa cells with a recombinant vaccinia virus expressing the hepatitis D antigen. Detection of c-myc mRNA sequences by means of in situ hybridization suggested that the c-myc product accumulation was not due to increased amounts of its mRNA. The c-myc protein accumulates selectively in the livers of patients with chronic hepatitis delta virus infection and in the same nuclei that contain the hepatitis D antigen. The expression of c-myc in hepatitis D antigencontaining cells does not require the presence of hepatitis B virus infection. (Hepatology 1994;20:1109–1114).

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