Hepatitis B virus (HBV) X gene mutations and their association with liver disease progression in HBV-infected patients
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60077344%3A_____%2F17%3A00483922" target="_blank" >RIV/60077344:_____/17:00483922 - isvavai.cz</a>
Result on the web
<a href="http://dx.doi.org/10.18632/oncotarget.22428" target="_blank" >http://dx.doi.org/10.18632/oncotarget.22428</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.18632/oncotarget.22428" target="_blank" >10.18632/oncotarget.22428</a>
Alternative languages
Result language
angličtina
Original language name
Hepatitis B virus (HBV) X gene mutations and their association with liver disease progression in HBV-infected patients
Original language description
Hepatitis B virus (HBV) is one of the most widespread human pathogens causing chronic hepatitis, liver cirrhosis, and hepatocellular carcinoma (HCC). This study investigated the clinical impact of single and combinational mutations in HBx gene on the pathogenesis of HCC during progressive stages of liver disease. The patients were categorized into inactive HBV carriers, active carriers, cirrhosis and HCC groups based on disease severity. Male sex, age > 50 years, and high serum alanine aminotransferase level were associated with risk of progressive liver disease. I127T, V131I, and F132Y/ I/R mutations showed a significant increasing trend associated with the disease progression to HCC. H94Y and K130M mutations were also significantly associated with severe liver disease. One double mutation (K130M+V131I) and two triple mutations (I127T+K130M+V131L and K130M+V131I+F132Y) were observed, with significant rising prevalence through progressive clinical phases of liver disease to HCC. Several single and combinational mutations in HBx correlating with severity and progressive clinical phases of HBV infection were identified. The mutational combinations may have a synergistic effect in accelerating the progression to HCC. These specific patterns of HBx mutations can be useful in predicting the clinical outcome of HBV-infected patients and may serve as early markers of high risk of developing HCC.
Czech name
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Czech description
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Classification
Type
J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database
CEP classification
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OECD FORD branch
10607 - Virology
Result continuities
Project
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Continuities
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Others
Publication year
2017
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
OncoTarget
ISSN
1949-2553
e-ISSN
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Volume of the periodical
8
Issue of the periodical within the volume
62
Country of publishing house
US - UNITED STATES
Number of pages
11
Pages from-to
105115-105125
UT code for WoS article
000419563600033
EID of the result in the Scopus database
2-s2.0-85036538804