Azar Saleh Shahbazi, Mansoori Maryam, Attar Marzieh, Shahbazi Majid
Medical Cellular and Molecular Research Center, Golestan University of Medical Sciences, Gorgan, Iran Email :
Asian Pac J Cancer Prev. 2016;17(7):3381-4.
Hepatitis B virus (HBV) is a key factor for hepatocellular carcinoma (HCC). About 350 million people are affected by chronic infection which is related to the rapid development of liver diseases as well as hepatitis, cirrhosis and hepatocellular carcinoma. Expression of tumor necrosis factor alpha (TNFα) in the liver demonstrates a major genetic polymorphism which is involved in resistance or susceptibility to chronic HBV infection.
In this study, two populations were studied by the sequence specific primerpolymerase chain reaction (SSPPCR) method: HBV cases (n=409), who were HBSAg+, and healthy controls (n=483).
The results shown that the frequency of TNFα 308 G/G genotype in healthy controls (47.2%) was significantly higher than in HBV infected patients (28%) (CI = 1.292.61, OR = 1.83, P = 0.0004). Also TNFα 308 A/A and A/G genotype frequencies in the healthy controls were 4.6% and 48.2% and in patient group were 19.5% and 52.5% (CI = 2.237.12, p: 0.0001, OR: 3.94) respectively.
We found that among Iranian people TNFα 308A allele not only has the highest genotype frequency but also it has the highest frequency in the world population. In addition, TNFα308 G/G polymorphism was associated with HBV resistance, whereas TNFα308A (A/A or A/G) polymorphism appeared to associated with chronic HBV infection. These data suggested that among the Iranian population, the 308 G/G polymorphism of TNFα gene promoter region has the potential to influence the susceptibility to HBV infection and it may be responsible for viral antigen clearance.
乙型肝炎病毒(HBV)是肝细胞癌(HCC)的关键因素。约3.5亿人受到慢性感染影响,这与肝脏疾病以及肝炎、肝硬化和肝细胞癌的快速发展有关。肝脏中肿瘤坏死因子α(TNFα)的表达表现出一种主要的基因多态性,其与慢性HBV感染的抗性或易感性有关。
在本研究中,通过序列特异性引物聚合酶链反应(SSPPCR)方法研究了两个人群:HBV病例(n = 409),即HBsAg阳性者,以及健康对照(n = 483)。
结果显示,健康对照中TNFα 308 G/G基因型的频率(47.2%)显著高于HBV感染患者(28%)(CI = 1.29 - 2.61,OR = 1.83,P = 0.0004)。此外,健康对照中TNFα 308 A/A和A/G基因型频率分别为4.6%和48.2%,患者组中分别为19.5%和52.5%(CI = 2.23 - 7.12,p:0.0001,OR:3.94)。
我们发现,在伊朗人群中,TNFα 308A等位基因不仅具有最高的基因型频率,而且在世界人群中也具有最高频率。此外,TNFα308 G/G多态性与HBV抗性相关,而TNFα308A(A/A或A/G)多态性似乎与慢性HBV感染相关。这些数据表明,在伊朗人群中,TNFα基因启动子区域的308 G/G多态性有可能影响对HBV感染的易感性,并且可能负责病毒抗原清除。