國家衛生研究院 NHRI:Item 3990099045/10074
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    題名: Expression of a hepatitis B virus pre-S2 deletion mutant in the liver results in hepatomegaly and hepatocellular carcinoma in mice
    作者: Teng, YC;Neo, JC;Wu, JC;Chen, YF;Kao, CH;Tsai, TF
    貢獻者: Institute of Molecular and Genomic Medicine
    摘要: Hepatocellular carcinoma (HCC) is the most common form of liver cancer and has a poor prognosis and a low survival rate; its incidence is on the rise. Hepatitis B virus (HBV) infection is one of the main causes of HCC. A high prevalence of pre-S deletions of HBV surface antigen, which encompass T-cell and/or B-cell epitopes, is found in HBV carriers; antiviral therapy and viral immune escape may cause and select for these HBV mutants. In particular, the presence of pre-S2 deletion mutants is an important risk factor associated with cirrhosis and HCC. We generated Alb-preS2 transgenic mice that express a naturally occurring pre-S2 mutant protein containing a 33-nucleotide deletion (preS2); the aim was to investigate its effect on hepatocarcinogenesis. After 30 months of follow-up, the liver pathology of the mice fell into four groups; G1, chronic inflammation solely; G2, chronic inflammation and fibrosis; G3, inflammation, fibrosis and hepatomegaly accompanied by rectal prolapse (4%-12%); and G4, hepatomegaly and spontaneous HCC (12%-15%). Striking degeneration of the endoplasmic reticulum (ER) was present in the mouse livers at an early stage (4-month old). At 8 months, overt ER stress and the Atf6 pathway of the unfolded protein response (UPR) were induced; at the same time metabolic pathways associated with mevalonate and cholesterol biogenesis, involving the peroxisomes and the ER, were disturbed. At 20 months and older, the protein kinase RNA-like endoplasmic reticulum kinase (PERK) pathway of the UPR was induced and the Hippo transducer Yap was activated. Together, these ultrastructural aberrations and metabolic disturbance all seem to contribute to the molecular pathogenesis and hepatocarcinogenesis present in the Alb-preS2 mice. These findings may inform the development of therapies for the liver disorders and HCC associated with pre-S2 deletion mutations among HBV carriers.
    日期: 2017-03
    關聯: Journal of Pathology. 2017 Mar;241(4):463-474.
    Link to: http://dx.doi.org/10.1002/path.4850
    JIF/Ranking 2023: http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=NHRI&SrcApp=NHRI_IR&KeyISSN=0022-3417&DestApp=IC2JCR
    Cited Times(WOS): https://www.webofscience.com/wos/woscc/full-record/WOS:000394898000004
    Cited Times(Scopus): http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85008173433
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