“…In particular, targeting in the liver, using an albumin promoter, of an accumulation of the large PreS1/S2/S HBV envelope protein induces a direct toxic effect on hepatocytes, independent of the immune response to the viral protein (Toshkov et al, 1994). In another context, the immune response to HBV-expressing hepatocytes in transgenic mice can also trigger such liver cell regeneration and give rise to HCC (Nakamoto et al, 1998;Chen et al, 2005b;Wang et al, 2005). Furthermore, HBV-positive, transgenic mice exhibit extensive oxidative DNA damage, possibly related to cytokine synthesis (Hagen et al, 1994;Hsieh et al, 2004); this observation may explain their increased sensitivity to chemical carcinogens and is probably relevant in humans exposed to both hepatitis viruses and chemical carcinogens (Bannasch et al, 1989;Sell, 1993).…”