Abed Sally, El-Dosoky Mohamed, El Sayed Zaki Maysaa, EL-Shafey Mohamed
Department of Tropical Medicine, Faculty of Medicine, Mansoura University, Egypt. Email:
Asian Pac J Cancer Prev. 2017 Oct 26;18(10):2683-2688. doi: 10.22034/APJCP.2017.18.10.2683.
Aim: The present study was performed to determine any associations of genetic polymorphisms of Fas/FasL promoter regions, at Fas670 and Fas1377 and FasL844, with hepatitis C cirrhosis and HCC, with a focus on severity of disease. Methods: Totals of 120 patients with cirrhosis and 101 with hepatocellular carcinoma (HCC) were enrolled. All had chronic HCV infection as indicated by positive anti-HCV antibodies and positive HCV RNA on real time PCR. One hundred healthy control subjects were also included in the study. Patients were subjected to full clinical, radiological and histopathological examinations. In addition to routine laboratory tests for liver function tests, Fas670 and Fas1377 and FasL844 genetic polymorphisms of Fas/FasL promoter regions were assessed by RFLP-PCR (restriction fragment length polymorphism with polymerase chain reaction). Results: Significant higher levels of the AG genotype in Fas670 and Fas1773 were observed in patients with cirrhosis and HCC (P=0.0001) as compared to control subjects. In addition, the CC genotype in FASL844 was also more common in patients (P=0.01). Furtehrmore, there was a significant association of substitution of A by G alleles in Fas670 and Fas1773 with advanced BCA staging (P=0.02, P=0.0001 respectively) and larger tumor size >5cm (P=0.01, P=0.0001 respectively) and in Fas670 with advanced pathological grading (P=0.0001). Moreover the CC genotype of FASL844 was significantly linked with advanced BCA, large tumor size >5cm and advanced pathological grading (P=0.0001). Conclusion: The findings of the present study highlight associations of genetic polymorphisms of promoter regions in Fas and Fas L with cirrhosis and HCC associated with chronic HCV. Support was also obtained for the conclusion that single nucleotide polymorphisms of the Fas/ FasL system impact on clinical and histopathological grading of HCCs. Further large scale studies are recommended for confirmation.
本研究旨在确定Fas/FasL启动子区域在Fas670、Fas1377和FasL844处的基因多态性与丙型肝炎肝硬化及肝癌之间的任何关联,重点关注疾病的严重程度。方法:招募了120例肝硬化患者和101例肝细胞癌(HCC)患者。所有患者抗-HCV抗体呈阳性且实时PCR检测HCV RNA呈阳性,表明均为慢性HCV感染。研究还纳入了100名健康对照者。对患者进行全面的临床、放射学和组织病理学检查。除了进行肝功能常规实验室检测外,通过RFLP-PCR(聚合酶链反应-限制性片段长度多态性)评估Fas/FasL启动子区域的Fas670、Fas1377和FasL844基因多态性。结果:与对照者相比,肝硬化和HCC患者中Fas670和Fas1773处的AG基因型水平显著更高(P = 0.0001)。此外,FASL844处的CC基因型在患者中也更常见(P = 0.01)。此外,Fas670和Fas1773中A等位基因被G等位基因替代与BCA晚期分期(分别为P = 0.02、P = 0.0001)、肿瘤大小>5cm(分别为P = 0.01、P = 0.0001)以及Fas670与病理高级别分级(P = 0.0001)存在显著关联。此外,FASL844的CC基因型与BCA晚期、肿瘤大小>5cm和病理高级别分级显著相关(P = 0.0001)。结论:本研究结果突出了Fas和Fas L启动子区域基因多态性与慢性HCV相关的肝硬化和HCC之间的关联。还支持了Fas/FasL系统的单核苷酸多态性影响HCC临床和组织病理学分级这一结论。建议进一步开展大规模研究以进行确认。