Volume 13, Issue 4 pp. 644-649
Original Article
Free Access

Expression of insulin-like growth factor II, α-fetoprotein and hepatitis B virus transcripts in human primary liver cancer

Elisabetta Cariani

Elisabetta Cariani

INSERM U 75, CHU Necker, Paris 75015; Unité d'Hépatologie, Hôpital Laënnec, 75340 Paris

Elisabetta Cariani was supported by a grant of the Commission of the European Communities.

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Chantal Lasserre

Corresponding Author

Chantal Lasserre

INSERM U 75, CHU Necker, Paris 75015; Unité d'Hépatologie, Hôpital Laënnec, 75340 Paris

INSERM U 75 CHU Necker, 156, rue de Vaugirard, 75015 Paris, France===Search for more papers by this author
François Kemeny

François Kemeny

Department of Hepatology and Surgery, Hôpital Evry, France

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Dominique Franco

Dominique Franco

Department of Hepatology and Surgery, Hôpital Evry, France

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Christian Brechot

Christian Brechot

INSERM U 75, CHU Necker, Paris 75015; Unité d'Hépatologie, Hôpital Laënnec, 75340 Paris

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First published: April 1991
Citations: 28

Abstract

Insulin-like growth factor II is a fetal growth factor structurally and functionally related to insulin and insulin-like growth factor I. Its mRNA expression is developmentally regulated in human liver, the reexpression of insulin-like growth factor II fetal transcripts being often observed in primary liver cancer. Insulin-like growth factor II and α-fetoprotein mRNAs were studied in 16 human primary liver cancers, most of which were highly differentiated. Hepatitis B virus transcripts were also analyzed in the tumors from hepatitis B virus chronic carriers. α-Fetoprotein mRNA was detected in only four tumors and in one nontumorous cirrhotic tissue; all these samples also displayed insulin-like growth factor II fetal transcripts. Furthermore, fetal insulin-like growth factor II mRNAs were observed in five tumors and six nontumorous cirrhotic areas not expressing α-fetoprotein mRNA. The presence of hepatitis B virus RNA was only observed in tissues not expressing α-fetoprotein or fetal insulin-like growth factor II mRNA. In conclusion, fetal insulin-like growth factor II transcripts are more frequently observed than α-fetoprotein mRNA in highly differentiated liver cancers and in surrounding cirrhotic areas. The reexpression of fetal insulin-like growth factor II transcripts might then be a marker of early steps of liver cell transformation. (HEPATOLOGY 1991;13:644–649.)

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