Association of-308G/A and-238G/A polymorphisms of TNF-α and osteosarcoma risk

被引:1
|
作者
Zhao, Zhongwei [1 ,2 ]
Tang, Xiangyu [1 ]
Song, Kai [1 ]
Li, Xiang [3 ]
Zhang, Yonggang [1 ]
机构
[1] Chinese Peoples Liberat Army Gen Hosp, Dept Orthopaed, Beijing 100835, Peoples R China
[2] Puren Hosp Beijing, Dept Orthopaed, Beijing 100062, Peoples R China
[3] Beijing Boai Hosp, China Rehabil Res Ctr, Dept Spine Surg, Beijing 100068, Peoples R China
关键词
TNF-alpha; polymorphisms; -308G/A; -238G/A; osteosarcoma; susceptibility; TUMOR-NECROSIS-FACTOR; GENE-EXPRESSION; CANCER; CELLS; DISEASE;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objective: As a proinflammatory cytokine, TNF-alpha is associated with increased risk of osteosarcoma (OS). Our study aimed to explore the association of TNF-alpha polymorphisms and OS susceptibility in the Han Chinese population. Methods: 80 OS patients and 99 healthy people, matched on the age and sex, participated in the study. Genotyping was conducted by the method of polymerase chain reaction-restricted fragment length polymorphisms (PCR-RFLP). Then logistic regression was used to evaluate the effects of TNF-alpha polymorphisms (-308G/A and -238G/A) on the pathology of OS. Results: The frequency of AA genotype in -308G/A locus in the cases was significantly higher than that of the healthy group (20.0% vs. 6.1%). Patients with OS were more likely to possess AA genotype of -308G/A locus (OR=4.00, 95% CI=1.41-11.38). For the patients with A allele, the risk for OS increased 0.62 fold (OR=1.62, 95% CI=1.04-2.50). There was no remarkable relationship of -238G/A polymorphisms and OS susceptibility. In addition, we found that patients with G-A and A-A haplotypes was much higher in the cases than that of control group (68.0% and 25.0%, 53.0% and 38.9%, respectively). A-G haplotype appeared to increase the risk for OS (OR=1.93, 95% CI=1.13-2.94). Conclusion: The AA genotype of -308G/A locus of TNF-alpha gene was a risk factor for OS, however there was no correlation between -238G/A of TNF-alpha and OS.
引用
收藏
页码:4177 / 4181
页数:5
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