HBV mutation literature information.


  Different precore/core mutations of hepatitis B interact with, limit, or favor liver fibrosis severity.
 PMID: 26992056       2016       Journal of gastroenterology and hepatology
Abstract: CONCLUSIONS: Patients with the A1762T/G1764A mutation have a higher risk of severe fibrosis.
Abstract: Interestingly, the association of the G1899A mutation with the double A1762T/G1764A mutant significantly counteracted the deleterious effect of the sole double A1762T/G1764A mutant (odds ratio [OR] = 0.28 vs.
Abstract: METHODS: Direct sequencing of the precore/core gene was used to detect A1762T/G1764A and G1757A mutations in the BCP and G1896A and


  Hepatitis B virus mutations, expression quantitative trait loci for PTPN12, and their interactions in hepatocellular carcinoma.
 PMID: 27075395       2016       Cancer medicine
Result: Of those 19 hotspot mutations, C1653T, T1674C/G, A1703G, G1719T, T1727A/G, T1753C, A1762T, G1764A, G1799C, G1899A,
Discussion: A1762T, G1764A, and T1753C/A mutations in the BCP region, and G1613A and C1653T mutations in the Enh II region were reported more frequent in HCC patients 27.


  Hepatitis B virus basal core promoter mutations show lower replication fitness associated with cccDNA acetylation status.
 PMID: 27132039       2016       Virus research
Abstract: HBV monomers bearing BCP mutations A1762T/G1764A and A1762T/G1764A/C1766T, and precore mutations G1896A, G1899A and G1896A/G1899A, were transfected into HepG2 cells using a plasmid-free approach.


  Genomic change in hepatitis B virus associated with development of hepatocellular carcinoma.
 PMID: 27340355       2016       World journal of gastroenterology
Abstract: Out of 240 CHB patients, 25 (10%) had C1653T and 33 (14%) had T1753V mutation in X region; 157 (65%) had A1762T/G1764A mutations in BCP region, 50 (21%) had G1896A mutation in precore region and 67 (28%) had pre-S deletions.


  Genetic diversity of hepatitis B virus and mutations associated to hepatocellular carcinoma in patients from Venezuela, with different stages of liver disease.
 PMID: 27382800       2016       Investigacion clinica
Abstract: Additionally, mutations were more common in early stages of liver disease in HBV subgenotype F2-infected patients, and a significant association between this subgenotype and the emergence of T 1753C, A1762T, A1762T/G1764A (p=0.04) and C1773T (p=0.001) mutations in chronic patients was found, when compared to the HBV subgenotype F3.
Abstract: By comparing F2 with all other HBV subgenotypes, a positive association for the three basal core promoter (BCP) mutants (A1762T, A1762T/G1764A p=0.01, G1764A p=0.04) was found.


  HBx mutations promote hepatoma cell migration through the Wnt/beta-catenin signaling pathway.
 PMID: 27420729       2016       Cancer science
Abstract: HBx mutations (T1753V, A1762T, G1764A, and T1768A) are frequently observed in hepatitis B virus (HBV)-related hepatocellular carcinoma (HCC).
Result: T1753A/A1762T/G1764A/T1768A mutations were rarely found in these samples (2-4%).
Result: The most frequently occurring mutation in this region was A1762T/G1764A, present in 20/50 (40%) HCC tissues and 19/50 (38%) non-tumorous tissues.


  Potential Susceptibility Mutations in C Gene for Hepatitis B-Related Hepatocellular Carcinoma Identified by a Two-Stage Study in Qidong, China.
 PMID: 27727182       2016       International journal of molecular sciences
Discussion: After adjustment for age, history of cigarette smoking and alcohol consumption, unconditional logistic regression analyses showed that pre-S deletion, C1653T, A1762T/G1764A, A2159G, A2189Y, G2203W, and C2288R mutations were significantly associated with high HCC risk.
Discussion: Meanwhile, the carcinogenic risk of pre-S deletion and pre-S2 start codon mutation in pre-S gene, C1653T, and A1762T/G1764A mutations in


  HBV core promoter mutations and AKT upregulate S-phase kinase-associated protein 2 to promote postoperative hepatocellular carcinoma progression.
 PMID: 27779207       2016       Scientific reports
Abstract: Results showed double mutation A1762T/G1764A (TA) combined with other mutation(s) (TACO) in HBV genome and phosphorylated AKT (pAKT) were more common in PHCC than BHCC.
Introduction: The double mutation A1762T/G1764A (TA) in the HBV basal core promoter (CP) region has been widely recognized to be independently associated with HCC.


  Hepatitis B Virus Core Promoter Double Mutations (A1762T, G1764A) Are Associated with Lower Levels of Serum Dihydrolipoyl Dehydrogenase.
 PMID: 27303803       2016       Intervirology
Abstract: OBJECTIVES: The aim of this study was to identify serum proteins with differential concentrations between hepatocellular carcinoma (HCC) patients and HBsAg asymptomatic carriers among individuals infected with hepatitis B virus (HBV) with basal core promoter (BCP) double mutations (A1762T, G1764A).


  Association study between mannose-binding lectin haplotypes and X gene mutation of hepatitis B virus from treatment naive patients.
 PMID: 27824315       2016       Aging
Result: However, we found that the medium/low MBL2 group has higher mutation rate in T1653, T1674, T1753, A1726T and G1764A when being compared with high MBL2 group, and significance was observed (Table 3 and Figure 2).
Table: G1764A



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