Hepatitis B virus (HBV) infection is one of the major risk factors in the development of hepatocullular carcinoma (HCC) worldwide. The therapy for HBV-related hepatocellular carcinoma (HCC) remains a major challenge in medicine considering the low response rate (usually below 10%) to current chemotherapy and the high relapsing rate (up to or beyond 50%) after surgery (1). Whether antivirals or interferon therapy for chronic HBV infection will offer a reduction or prevention of HCC development remains to be clarified (2). There are several reasons to explain the difficulty or failure to treat HCC. One reason may lie in the inherent nature of the liver which is the organ responsible for the metabolism of chemicals and drugs. The second reason is the heterogenecity of HCCs and complex mechanisms of HBV tumorigenesis which make the choice of therapies difficult (3). Although current advances in cancer genomics have tried to identify the potential HCC biomarkers and molecular classification of HCC is proposed (4), their application to clinical therapy remains to be verified.
Due to the difficulty of therapy for HCCs, many efforts have currently turned to prevent HCC development during the long course of chronic HBV infection. In the paper published in
HBV tumorigenesis may include host factors associated anti-viral immune response and viral factors associated with insertional mutagenesis and expression of viral oncoproteins (8). The host factor-driven tumorigenesis may prevail at the early stage of HBV infection associated with CD8-mediated immune response, resulting in inflammation, liver injuries, liver fibrosis and regeneration, and finally HCC development as described by the same group in their previous reports (9). In this scenario, the anti-platelet therapy as reported by Sitia et al. will provide the candidate agents for prevention of HCC development at the high replicative stage of chronic HBV infection. Both Asp and Clo are suitable for preventive therapy considering the long-term usage and low toxicity in patients with chronic HBV infection. However, the viral oncoproteins-driven HBV tumorigenesis usually develops HCCs at the low or non-replicative phase of chronic HBV infection (Figure 1). The hepatocytes harboring the mutated viral oncoproteins escape from the immune attack and series of biologic events are initiated by viral oncoproteins to develop HCC (10). In this case, the immune-mediated antiplatelet therapy will be less effective for the prevention of HCC and other preventive measures should be searched for. Both the recognized HBV oncoproteins HBx and pre-S2 deletion mutants have been found to induce fatty livers through the induction of endoplasmic reticulum (ER) stress, inflammation, dysregulated lipid metabolism, and activation of NFκB and mTOR signaling by viral oncoproteins (11,12). Lipid metabolism is disturbed at the advanced stage of chronic liver disease including chronic HBV and HCV infection, and carries a significantly increased risk of HCC development (13,14). Therefore, ameliorating lipid metabolism may provide an alternative target for preventing HCC development. Several agents have been tried for cancer prevention, including agonists of peroxisome proliferator activated receptors (PPAR), unsaturated fatty acids, and extracts of natural products (15).
To clarify the underlying pathogenesis and mechanism of HBV tumorigenesis is critical not only for the preventive therapy for high risk chronic HBV infection patients but can also identify the driven signaling or early biologic events for developing target therapy for HCCs. The development of HCC is a highly heterogeneous process that involves host immune mediated phase in the early infection stage and immune escape phase in the late infection stage. Chronic liver injury and the attendant inflammatory and regenerative responses create CD8-mediated tumorigenesis that provides a scenario of hepatocarcinogenesis. As the disease progresses, viral proteins escape immune attack via mutation and initiate a series of viral oncoproteins-driven tumorigenesis pathways which could contribute to 50% of the HCC development in humans (Figure 1). As mentioned above, human HBV-related HCCs are complicated and we may need personalized therapy which targets at pathways specific for the patients or the driving signals specific for each tumor in the future.
This project is supported by grants from National Science Council and National Health Research Institutes (Dr. Su IJ).
Disclosure: The authors declare no conflict of interest.
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