期刊论文详细信息
Journal of Experimental & Clinical Cancer Research
FOXP3 gene polymorphism is associated with hepatitis B-related hepatocellular carcinoma in China
HongSong Chen1  Lai Wei1  LiLing Qin2  Ran Fei1  XingWang Xie1  GaiXia He1  JinXue Zhou3  WeiJia Liao2  HengHui Zhang1  YanHui Chen1 
[1] Beijing Key Laboratory of Hepatitis C and Immunotherapy for Liver Diseases, Beijing 100044, P. R. China;Affiliated Hospital of Guilin Medical University, Guilin 541004, P. R. China;Department of Hepatobiliary and Pancreatic Surgery, Henan Tumor Hospital, Zhengzhou 450008, P. R. China
关键词: FOXP3;    Gene polymorphism;    Chronic;    Hepatitis B;    Hepatocellular;    Carcinoma;   
Others  :  824942
DOI  :  10.1186/1756-9966-32-39
 received in 2013-02-06, accepted in 2013-05-28,  发布年份 2013
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【 摘 要 】

Background

Previous evidence has shown that the FOXP3 gene was involved in the pathogenesis of several tumors; however, the correlation between single nucleotide polymorphisms (SNPs) in the FOXP3 gene and the susceptibility to hepatitis B-related hepatocellular carcinoma (HCC) remains unclear.

Methods

We analyzed two SNPs in the FOXP3 gene, rs2280883 and rs3761549, in 392 patients with HCC, 344 patients with chronic hepatitis B (CHB) and 372 matched healthy controls. Genotyping was performed by MALDI-TOF Mass Spectrometry for all donors.

Results

Compared to healthy controls, HCC patients had higher frequencies of the TT genotype (79.6%) at rs2280883 and the CC genotype (77.6%) at rs3761549 of the FOXP3 gene; CHB patients also had higher frequencies of the TT genotype (74.1%) at rs2280883 and the CC genotype (74.6%) at rs3761549. There were no significant differences in the distribution of FOXP3 genotypes between CHB donors and HCC donors. The TT genotype at rs2280883 was more frequent in patients with HCC than healthy donors (P = 0.01), but no significant difference was observed in this genotype between CHB and healthy donors (P = 0.479). C allele frequency at rs3761549 was higher in HCC patients than healthy donors (P = 0.03), but distribution of this allele was not significantly different between CHB patients and healthy donors (P = 0.11). Stratified analysis showed that the CC genotype at rs3761549 was significantly associated with a high incidence of portal vein tumor thrombus (P = 0.02) and that the TT/CT genotype at rs3761549 was significantly associated with an increased rate of tumor recurrence in HCC patients (P = 0.001).

Conclusions

Our results suggested that the FOXP3 gene polymorphisms at rs2280883 and rs3761549 may be associated with hepatitis B-related HCC. At rs3761549, the CC genotype and the TT/CT genotype were associated with a high incidence of portal vein tumor thrombus and tumor recurrence, respectively.

【 授权许可】

   
2013 Chen et al.; licensee BioMed Central Ltd.

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