Evolutionary Changes of Hepatitis B Virus Pre-S Mutations Prior to Development of Hepatocellular Carcinoma

被引:12
|
作者
Zhang, An-Ye [1 ]
Lai, Ching-Lung [1 ,2 ]
Huang, Fung-Yu [1 ]
Seto, Wai-Kay [1 ,2 ]
Fung, James [1 ,2 ]
Wong, Danny Ka-Ho [1 ,2 ]
Yuen, Man-Fung [1 ,2 ]
机构
[1] Univ Hong Kong, Dept Med, Hong Kong, Hong Kong, Peoples R China
[2] Univ Hong Kong, State Key Lab Liver Res, Hong Kong, Hong Kong, Peoples R China
来源
PLOS ONE | 2015年 / 10卷 / 09期
关键词
INTRACELLULAR RETENTION; SURFACE-ANTIGEN; CELL EPITOPES; GENOTYPE-B; RISK; DELETIONS; PROTEIN; MUTANT;
D O I
10.1371/journal.pone.0139478
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background and Aims Deletions/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. Methods We 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. Results Compared to the HCC-free group, higher frequencies of pre-S deletions and pointmutations (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 andmost 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). Conclusions High 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.
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页数:14
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