G-308A TNF-α polymorphism is associated with an increased risk of hepatocellular carcinoma in the Turkish population: Case-control study

2009 ◽  
Vol 33 (3-4) ◽  
pp. 261-264 ◽  
Author(s):  
Hikmet Akkız ◽  
Süleyman Bayram ◽  
Aynur Bekar ◽  
Burhan Özdil ◽  
Ersin Akgöllü ◽  
...  
2011 ◽  
Vol 39 (2) ◽  
pp. 1639-1647 ◽  
Author(s):  
Ahmet Taner Sümbül ◽  
Hikmet Akkız ◽  
Süleyman Bayram ◽  
Aynur Bekar ◽  
Ersin Akgöllü ◽  
...  

2010 ◽  
Vol 28 (6) ◽  
pp. 369-376 ◽  
Author(s):  
Mohammad Asim ◽  
Luqman A. Khan ◽  
S. A. Husain ◽  
Sajid Husain ◽  
Manash P. Sarma ◽  
...  

Objective:Our aim was to evaluate whether the association of GSTM1/T1 gene polymorphisms modifies the risk of Hepatocellular carcinoma (HCC) and what is its correlation with other predisposing risk factors like alcohol intake, cigarette smoking and hepatitis B and C infections.Study design/setting:It was a case-control study, included 254 HCC cases compared with 525 hospital-based age and sex matched cases of chronic liver disease without HCC as controls from Indian population. The GSTM1 and GSTT1 genotypes were detected using conventional multiplex PCR method.Results:In this case-control study, we observed a positive correlation between age, HBV and HCV infection, smoking habit of > 20 packs/year, alcohol consumption of > 100 g/day and risk of liver cancer. We found significantly increased risk associated with GSTM1 null genotype (OR = 3.49; 95% CI = 2.52–4.84) as well as GSTT1 null genotype (OR = 3.12; 95% CI = 2.19–4.45), respectively. However, an increased risk of HCC was observed among heavy drinkers with GSTM1 (OR = 2.01; 95% CI = 1.11–3.66). Further, cigarette smoking showed a non-significant association with GSTT1 (OR = 1.49; CI = 0.69–3.25).Conclusion:Our results suggest that the variants in low penetrance gene such as GSTM1 and GSTT1 are associated with an increased liver cancer risk. Further, an influence of GSTM1/T1 null genotypes may contribute in the etiology of HCC in patients with higher cigarette and alcohol consumption.


2011 ◽  
Vol 39 (5) ◽  
pp. 5943-5951 ◽  
Author(s):  
Süleyman Bayram ◽  
Hikmet Akkız ◽  
Aynur Bekar ◽  
Ersin Akgöllü ◽  
Selçuk Yıldırım

Gene ◽  
2011 ◽  
Vol 486 (1-2) ◽  
pp. 104-109 ◽  
Author(s):  
Hikmet Akkız ◽  
Süleyman Bayram ◽  
Aynur Bekar ◽  
Ersin Akgöllü ◽  
Oğuz Üsküdar ◽  
...  

2011 ◽  
Vol 26 (3) ◽  
pp. 181-187 ◽  
Author(s):  
Xiangmei Chen ◽  
Ling Zhang ◽  
Yibin Chang ◽  
Tao Shen ◽  
Ling Wang ◽  
...  

The single nucleotide polymorphisms (SNPs) within the tumor necrosis factor-α (TNF-α) gene promoter region have been reported to be associated with susceptibility to various types of cancers. A case-control study (126 hepatocellular carcinoma [HCC] patients and 126 normal controls) was conducted to elucidate their possible association with the risk of hepatitis B virus (HBV)-related HCC in a Han Chinese population. TNF-α polymorphisms -1031T/C, -863C/A, -857C/T, -308G/A, and -238G/A were genotyped by polymerase chain reaction (PCR) and direct DNA sequencing. Disease associations were analyzed by the chi-square test or Fisher's exact test. When analyzed by overall groups, no significant differences in genotype and allele distributions were observed between the control and cases. However, stratified analysis according to sex showed that the frequency of the homozygous C allele of the -857 polymorphism was lower in female cases than in female controls (62.9% vs. 88.9%, p=0.026). In addition, further haplotype analysis revealed that the TCCGA (-1031/-863/-857/-308/-238) was more frequent in controls than cases (p=0.018; odds ratio = 0.266; 95% confidence interval, 0.083–0.857). These results indicated that the TNF-α-857C/T polymorphism may modify HBV-related HCC risk among women, and the haplotype TCCGA (-1031/-863/-857/-308/-238) may account for a decreased susceptibility to HCC development in the Han Chinese population. Additional studies in patients with different ethnic backgrounds are needed to validate these finding and to further explore the genetic pathogenesis of HBV-related HCC.


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