Novel natural mutations in the hepatitis B virus reverse transcriptase domain associated with hepatocellular carcinoma

PLoS One. 2014 May 1;9(5):e94864. doi: 10.1371/journal.pone.0094864. eCollection 2014.

Abstract

Background/aim: Hepatitis B Virus (HBV) mutations play a role in the development of hepatocellular carcinoma (HCC). However, the association between HBV polymerase gene mutations and HCC has not been reported. In this study, we conducted a multi-stage study to identify HCC-related mutations in the reverse transcriptase (RT) domain of the HBV polymerase gene.

Methods: A total of 231 HCCs and 237 non-HCC controls from Qidong, China, were included in this study. The entire sequence of HBV RT was first compared between 29 HCC and 35 non-HCC cases, and candidate mutations were then evaluated in two independent validation sets.

Results: There were 15 candidate mutations identified from the discovery set, with A799G and T1055A being consistently associated with HCC across all studies. A pooled analysis of samples revealed that A799G, A987G, and T1055A were independent risk factors for HCC, with adjusted odds ratios of 5.53 [95% confidence interval (CI), 1.69-18.10], 4.20 (95%CI, 1.15-15.35), and 3.78 (95%CI, 1.45-9.86), respectively. A longitudinal study showed that these mutations were detectable 4-5 years prior to HCC diagnosis.

Conclusions: Our study provides evidence the first that HBV RT contains naturally occurring mutations that can be used as predictive markers for HCC.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Alleles
  • Amino Acid Substitution
  • Carcinoma, Hepatocellular / etiology*
  • Case-Control Studies
  • Female
  • Hepatitis B / complications*
  • Hepatitis B / virology*
  • Hepatitis B virus / genetics*
  • Humans
  • Liver Neoplasms / etiology*
  • Male
  • Middle Aged
  • Mutation Rate
  • Odds Ratio
  • RNA-Directed DNA Polymerase / genetics*
  • Reproducibility of Results
  • Risk Factors
  • Viral Load

Substances

  • RNA-Directed DNA Polymerase