Abstract

Background and AimsDeletions/mutations in the hepatitis B virus (HBV) pre-S region have been associated with hepatocellular carcinoma (HCC). We aimed to study the evolutionary changes of pre-S mutations prior to HCC development.MethodsWe studied the HBV pre-S sequences at 1 to 10 years preceding diagnosis of HCC in 74 patients with HBV-related HCC (HCC group). 148 chronic hepatitis B patients matched for sex and age in 2:1 ratio, who had been followed up for at least 3 years without HCC (HCC-free group) were recruited as controls. 56 and 47 patients of HCC and HCC-free groups respectively had serially stored sera for longitudinally examination at 1–3 years, 4–6 years, 7–9 years and ≥10 years prior to the recruitment of the study.ResultsCompared to the HCC-free group, higher frequencies of pre-S deletions and point mutations (at 11 codons) were observed in the HCC group (p<0.05). Multiple logistic regression analysis showed that pre-S deletions, point mutations at codon 51 and 167 were independent factors associated with HCC. Longitudinal observation showed that pre-S deletions and most of the 11 HCC-associated pre-S point mutations existed at least 10 years before HCC development, and were more prevalent preceding HCC development in patients from HCC groups than HCC-free group. The number of HCC-associated pre-S point mutations increased over time preceding HCC development, and correlated positively with the time to HCC diagnosis (r = 0.220, p = 0.005).ConclusionsHigh prevalence and cumulative evolution of pre-S mutations preceding HCC development suggested a possible carcinogenic role of pre-S mutations and their potential application in HCC risk prediction.

Highlights

  • Hepatocellular carcinoma (HCC) is the third major cause of cancer-related mortality in the world, with an estimated annual death rate of 700,000 [1]

  • We studied the hepatitis B virus (HBV) pre-S sequences at 1 to 10 years preceding diagnosis of hepatocellular carcinoma (HCC) in 74 patients with HBV-related HCC (HCC group). 148 chronic hepatitis B patients matched for sex and age in 2:1 ratio, who had been followed up for at least 3 years without HCC (HCCfree group) were recruited as controls. 56 and 47 patients of HCC and HCC-free groups respectively had serially stored sera for longitudinally examination at 1–3 years, 4–6 years, 7–9 years and 10 years prior to the recruitment of the study

  • Multiple logistic regression analysis showed that pre-S deletions, point mutations at codon 51 and 167 were independent factors associated with HCC

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Summary

Introduction

Hepatocellular carcinoma (HCC) is the third major cause of cancer-related mortality in the world, with an estimated annual death rate of 700,000 [1]. Hepatitis B virus (HBV) infection is one of the major causes of HCC. Pre-S region contains start codons for the expression of large and middle HBV surface antigens (LHBs and MHBs, respectively), and promoter for the expression of small HBV surface antigen (SHBs). It contains both B- and T-cell epitopes that mediate immune interactions, hepatocyte binding sites that participate in viral attachment, and other functional domains (Fig 1) [4,5,6,7,8,9]. Deletions/mutations in the hepatitis B virus (HBV) pre-S region have been associated with hepatocellular carcinoma (HCC).

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