Jung Yong Jin, Kim Yoon Jun, Kim Lyoung Hyo, Lee Soo Ok, Park Byung Lae, Shin Hyoung Doo, Lee Hyo-Suk
Department of Internal Medicine and Liver Research Institute, Seoul National University College of Medicine, Seoul, Korea.
Intervirology. 2007;50(5):369-76. doi: 10.1159/000109751. Epub 2007 Oct 15.
Fas/FasL polymorphisms, which are related to apoptosis, might influence the clearance of hepatitis B virus (HBV) infection and the occurrence of hepatocellular carcinoma (HCC). This study was performed to determine whether Fas and FasL promoter polymorphisms are associated with clinical outcome in chronic HBV infection.
A total of 1,095 Korean subjects were prospectively allocated to two different groups: 'the chronic carrier group' (CC; n = 666), who were repeatedly hepatitis B surface antigen (HBsAg)-positive, and 'the spontaneous recovery group' (SR; n = 429), who were HBsAg-negative with antibodies to HBsAg and hepatitis B core antigen. In addition, the CC group was subcategorized into chronic hepatitis and HCC subgroups. Fas promoter polymorphisms at -1377G>A and -670A>G and the FasL promoter polymorphism at -844C>T were analyzed for and the genotype distributions of subjects were compared.
There were no significant associations between Fas or FasL promoter polymorphism with the HBV clearance and HBeAg clearance. However, -1377G>A in Fas promoter region showed protective effect to HCC occurrence (RH = 0.70, p = 0.03).
Fas-1377G>A polymorphisms might be involved in the pathogenesis of human HCC.
与细胞凋亡相关的Fas/FasL基因多态性可能影响乙型肝炎病毒(HBV)感染的清除及肝细胞癌(HCC)的发生。本研究旨在确定Fas和FasL启动子多态性是否与慢性HBV感染的临床结局相关。
1095名韩国受试者被前瞻性地分为两个不同组:“慢性携带者组”(CC;n = 666),其乙肝表面抗原(HBsAg)反复呈阳性;“自发恢复组”(SR;n = 429),其HBsAg呈阴性且有抗HBsAg和乙肝核心抗原抗体。此外,CC组又被细分为慢性肝炎和HCC亚组。分析了Fas启动子-1377G>A和-670A>G多态性以及FasL启动子-844C>T多态性,并比较了受试者的基因型分布。
Fas或FasL启动子多态性与HBV清除及HBeAg清除之间无显著关联。然而,Fas启动子区域的-1377G>A对HCC发生具有保护作用(相对危险度=0.70,p = 0.03)。
Fas -1377G>A多态性可能参与人类HCC的发病机制。