H. Unsal et al., GENETIC-HETEROGENEITY OF HEPATOCELLULAR-CARCINOMA, Proceedings of the National Academy of Sciences of the United Statesof America, 91(2), 1994, pp. 822-826
We studied 80 hepatocellular carcinomas from three continents For p53
gene (TP53) mutations and hepatitis B virus (HBV) sequences. p53 mutat
ions were frequent in tumors from Mozambique but not in tumors from So
uth Africa, China, and Germany. Independent of geographic origin, most
tumors were positive for HBV sequences. X gene coding sequences of HB
V were detected in 78% of tumors, whereas viral sequences in the surfa
ce antigen- and core antigen-encoding regions were present in less tha
n 45% of tumors. These observations indicate that hepatocellular carci
nomas are genetically heterogeneous. Mozambican-type of hepatocellular
carcinomas are characterized by a high incidence of p53 mutations rel
ated to aflatoxins. In other tumors, the rarity of p53 mutations combi
ned with the frequent presence of viral X gene coding sequences sugges
ts a possible interference of HBV with the wild-type p53 function.