MMP9和CEBPα基因作为hcv基因型感染引起的肝细胞癌新的预后生物标志物(4)

R. S. Hamad, N. K. A. Abdulsalam, A. Mashaal, R. El-Araby
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摘要

肝细胞癌(HCC)仍然是肝癌的主要类型。了解HCC肿瘤发生的分子和免疫机制是开发有效生物标志物的必要条件。本研究旨在检测循环MMP9和CEBPα,为hcv基因型(4)诱导的肝硬化和癌变提供诊断和预后的生物标志物。这项研究包括100名埃及患者,分为两组,每组50名患者。第一组:分为无肝硬化慢性肝病(CLD) (n=25)和合并肝硬化慢性肝病(CLD) (n=25)。第二组:分为CLD合并HCC患者(25例)和健康对照组(25例)。Real-Time PCR检测MMP9和CEBPα基因的表达。我们的研究结果显示肝硬化和HCC患者的MMP9和CEBPα基因分别显著下调(p< 0.001和p<0.001)。HCC患者与CLD合并或不合并肝硬化患者之间的诊断能力显著(p< 0.001)。生物信息学分析揭示了MMP9与CEBPα基因之间的关系。总之,在疾病进展过程中,MMP9和CEBPα基因的表达逐渐减少,推荐使用MMP9和CEBPα基因作为hcv基因型患者肝硬化和HCC的诊断和预后生物标志物(4)。
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MMP9 and CEBPα Genes as a New Prognostic Biomarker for Hepatocellular Carcinoma Caused by Infection with HCV-Genotype (4)
Hepatocellular carcinoma (HCC) remains the main type of liver cancer. Understanding the molecular and immune mechanisms of HCC tumorigenesis are required to develop effective biomarkers. This study is designed to measure the circulating MMP9 and CEBPα to provide a diagnostic and prognostic biomarker for HCV-genotype (4) induced liver cirrhosis and carcinogenesis. This study included one hundred Egyptian patients, divided into two groups 50 patients each. The first group: classified into Chronic Liver Disease (CLD) without cirrhosis (n=25) and CLD with cirrhosis (n=25). The second group: classified into CLD patients with HCC, (n=25), and healthy control (25 volunteers). The expression of MMP9 and CEBPα genes were analysed using Real-Time PCR. Our results showed significant downregulation in MMP9 and CEBPα genes in cirrhotic and HCC patients (p< 0.001 and p<0.001) respectively. There was a significant (p< 0.001) diagnostic capacity between HCC patients against CLD with or without cirrhosis patients. Bioinformatics analysis revealed a relationship between MMP9 and CEBPα genes. In conclusion, the gradual decrease in the expression of MMP9 and CEBPα gene during the progression of the disease recommended use of MMP9 and CEBPα genes as a diagnostic and prognostic biomarker for both cirrhosis and HCC in HCV-genotype (4) patients.
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