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Detection of BCL2 Polymorphism in Patient with Hepatocellular Carcinoma

机译:肝细胞癌患者BCL2基因多态性的检测

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Introduction: Despite advances in the knowledge of the molecular virology of hepatitis C virus (HCV), the mechanisms of hepatocellular injury in HCV infection are not completely understood. Hepatitis C viral infection (HCV) influences the susceptibility to apoptosis. This could lead to insufficient antiviral immune response and persistent viral infection. Aim of this study: Is to examine whether BCL-2 gene polymorphism at codon 43 (+127G/A or Ala43Thr) has an impact on development of hepatocellular carcinoma caused by chronic hepatitis C infection among Egyptian patients. Subjects and Methods: The study included three groups; group 1: composed of 30 patients with hepatocellular carcinoma (HCC), group 2 composed of 30 patients with chronic hepatitis C infection (CHC) and group 3 composed of 30 healthy subjects matching the same age and socioeconomic status were taken as a control group. Gene polymorphism of BCL2 (Ala43Thr) was evaluated by Restriction fragment length polymorphism (PCR-RFLP) techniqueand measured for all patients and controls. Results: The summed 43Thr genotype was more frequent and statistically significant in HCC patients as compared to control group. This genotype of BCL2 gene may inhibit the programmed cell death which leads to disturbance in tissue and cells homeostasis and reduction in immune regulation. This result leads to viral replication and HCV persistence. Moreover, virus produces variety of mechanisms to block genes participated in apoptosis. This mechanism proves that CHC patients who have 43Thr genotype are more susceptible to HCC. Correlation coefficients between AFP versus ALT and AST were statistically significant. Conclusion: The data investigated for the first time that BCL2 polymorphism is associated with the susceptibility to in Egyptian populations and might be used as molecular markers for evaluating risk. This study clearly demonstrated that CHCexhibit a deregulation of apoptosis with the disease progression. This provides an insight into the pathogenesis of chronic hepatitis C infection, and may contribute to the therapy.
机译:简介:尽管对丙型肝炎病毒(HCV)的分子病毒学知识有了新的了解,但对HCV感染中肝细胞损伤的机制尚未完全了解。丙型肝炎病毒感染(HCV)影响细胞凋亡的敏感性。这可能导致抗病毒免疫反应不足和持续的病毒感染。这项研究的目的是要检查埃及患者中第43位密码子(+ 127G / A或Ala43Thr)的BCL-2基因多态性是否对由慢性丙型肝炎感染引起的肝细胞癌的发展产生影响。受试者与方法:该研究包括三组。第1组:30例肝细胞癌(HCC);第2组:30例慢性丙型肝炎(CHC)患者;第3组,由30名年龄和社会经济状况相同的健康受试者组成。通过限制性片段长度多态性(PCR-RFLP)技术评估了BCL2(Ala43Thr)的基因多态性,并测量了所有患者和对照。结果:与对照组相比,HCC患者的总43Thr基因型更为常见,并具有统计学意义。 BCL2基因的这种基因型可能会抑制程序性细胞死亡,从而导致组织和细胞体内平衡紊乱并降低免疫调节。该结果导致病毒复制和HCV持久性。而且,病毒产生多种机制来阻断参与细胞凋亡的基因。这种机制证明,具有43Thr基因型的CHC患者更容易感染HCC。 AFP与ALT和AST之间的相关系数具有统计学意义。结论:首次调查的数据表明,BCL2基因多态性与埃及人群的易感性有关,可作为评估风险的分子标记。这项研究清楚地表明,CHC会随着疾病的发展而抑制细胞凋亡。这为慢性丙型肝炎感染的发病机理提供了见识,并可能有助于治疗。

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