Influence of transforming growth factor-β1 and tumor necrosis factor-α genes polymorphisms on the development of cirrhosis and hepatocellular carcinoma in chronic hepatitis C patients

被引:60
作者
Radwan, Mohamed I. [2 ]
Pasha, Heba F. [1 ]
Mohamed, Rasha H. [3 ]
Hussien, Hala I. M. [2 ]
El-Khshab, Mohamed N. [2 ]
机构
[1] Zagazig Univ, Fac Med, Dept Med Biochem, Zagazig, Egypt
[2] Zagazig Univ, Dept Trop Med, Fac Med, Zagazig, Egypt
[3] Zagazig Univ, Dept Biochem, Fac Pharm, Zagazig, Egypt
关键词
Transforming growth factor-beta 1; Tumor necrosis factor-alpha; Hepatitis C virus; Hepatocellular carcinoma; Cirrhosis; LIVER FIBROSIS; PROMOTER POLYMORPHISM; TGF-BETA; INFLAMMATION; ASSOCIATION; RISK; PROGRESSION; CANCER; ANGIOGENESIS; CYTOKINES;
D O I
10.1016/j.cyto.2012.05.010
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Background: Host genetic factors may affect clinical outcomes of hepatitis C virus (HCV) infection; however, the possible mechanisms remain largely unknown. This study aimed to evaluate transforming growth factor-beta 1 (TGF-beta 1)-509 and tumor necrosis factor-a (TNF-alpha)-308 genes polymorphisms as a risk factors for cirrhosis and hepatocellular carcinoma (HCC) in chronic hepatitis C patients. Materials and methods: Two hundred and eighty HCV patients (152 patients with cirrhosis, 128 patients with HCC) and 160 controls were enrolled in the study. Polymorphisms of TGF-beta 1-509 and TNF-alpha-308 gene were determined using polymerase chain reaction restriction fragment length polymorphism (PCR-RFLP). Serum TGF-beta 1 and TNF-alpha were determined using ELISA. Results: TGF-1 beta-509 TT, TNF-alpha-308 AA and GA genotypes frequencies were significantly increased in cirrhotic and HCC groups. Serum TGF-beta 1 and TNF-alpha level were significantly increased in TGF-beta 1-509 IT and TNF-alpha-308 M genotypes respectively. Conclusion: TGF-beta 1-509 and INF-alpha-308 genes polymorphisms are associated with risk of liver cirrhosis and HCC in patients with chronic HCV infection. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:271 / 276
页数:6
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