测量原发性肝细胞癌组织中主要高甲基化肿瘤抑制基因的差异表达

IF 3.5 Q3 Biochemistry, Genetics and Molecular Biology
Khalda Sayed Amr , Wafaa Mohamed Ezzat , Ahmed Ibrahim Saleh , Ahmed Heiba , Hend Amin , Refaat Refaat Kamel , Noha Eltaweel , Hoda Henery , Amr Omaia , Reham Ibrahim Siddik , Yasser Abdelghany Abdelazeem Elhosary
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引用次数: 0

摘要

背景肝癌的发生是一个多因素过程,由遗传和表观遗传异常整合而成,导致基因表达和功能异常。很难用单一的生物标志物来描述 HCC 的特征。我们的研究旨在检测埃及 HCC 患者中作为调控因素的 8 个甲基化基因(SOCS1、APC、Gadd45b、CDKN1B、P15、PAX6、STAT1 和 MSH2)的表达。组织样本来自在埃及开罗萨赫勒教学医院(El Sahel Teaching Hospital)接受活体肝移植(LDLT)或肝切除术的患者。结果与肝硬化组织相比,SOCS1、APC、Gadd45b、CDKN1B、P15、PAX6、STAT1 和 MSH2 在 HCC 组织中的表达量较低(pvalue 分别为 0.015、0.081、0.004、0.027、0.211、0.015、0.025 和 0.0001)。5个基因(SOCS1、APC、GAdd45b、CDKN1B和MSH2)显示出了作为HCC诊断生物标志物的能力,其敏感性和特异性在切点值上都很高:分别为 1.05、1.17、0.995、0.546 和 0.125。至于其他 3 个基因(P15、PAX6 和 STAT1),PAX6 基因的灵敏度最高,截断值为 0.3364。结论所选的高甲基化基因(SOCS1、APC、Gadd45b、CDKN1B、P15、PAX6、STAT1 和 MSH2)在 HCC 组织样本中的表达量低于邻近组织。应进一步研究这些基因的作用,以解开围绕 HCC 发病机制的谜团。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Measuring the differential expression of the major hypermethylated tumor suppressor genes in tissues of primary hepatocellular carcinoma

Background

Hepatocarcinogenesis is a multifactorial process that arises from a integration of genetic and epigenetic anomalies leading to abnormal gene expression and function. It is difficult to characterize HCC with a single biomarker. Our study aimed at detecting the expression of a panel of 8 methylated genes (SOCS1, APC, Gadd45b, CDKN1B, P15, PAX6, STAT1 and MSH2) as regulatory factors among Egyptian patients with HCC.

Methods

This study was conducted on HCC tissue samples of 30 Egyptian patients in comparison with their non-cancerous adjacent cirrhotic tissue as a control. Tissue samples were obtained from patients who have undergone living donor liver transplantation (LDLT) or liver resection at El Sahel Teaching Hospital (Cairo, Egypt). A special Custom designed PCR Arrays was used to analyze the expression profiles of chosen methylated genes associated with HCC.

Results

Expression of SOCS1, APC, Gadd45b, CDKN1B, P15, PAX6, STAT1 and MSH2 were lower in the HCC tissue compared to the cirrhotic tissue (pvalue = 0.015, 0.081, 0.004, 0.027, 0.211, 0.015, 0.025 and 0.0001 respectively). 5 genes (SOCS1, APC, GAdd45b, CDKN1B, and MSH2) showed the ability to be used as diagnostic biomarkers for HCC with high sensitivity and specificity values at cut off values: 1.05, 1.17, 0.995, 0.546, and 0.125 respectively. As for the other 3 genes (P15, PAX6, STAT1), PAX6 gene has the highest sensitivity at a cut off value of 0.3364. A significant negative correlation was shown between alpha fetoprotein (AFP) and 5 of the studied genes (SOCS1, APC, Gadd45b, STAT1, and MSH2).

Conclusions

Expression of the selected hypermethylated genes (SOCS1, APC, Gadd45b, CDKN1B, P15, PAX6, STAT1 and MSH2) in HCC tissue samples was lower than adjacent tissue. Their role should be further studied to solve the mystery that surrounds the pathogenesis of HCC.

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来源期刊
Journal of Genetic Engineering and Biotechnology
Journal of Genetic Engineering and Biotechnology Biochemistry, Genetics and Molecular Biology-Biotechnology
CiteScore
5.70
自引率
5.70%
发文量
159
审稿时长
16 weeks
期刊介绍: Journal of genetic engineering and biotechnology is devoted to rapid publication of full-length research papers that leads to significant contribution in advancing knowledge in genetic engineering and biotechnology and provide novel perspectives in this research area. JGEB includes all major themes related to genetic engineering and recombinant DNA. The area of interest of JGEB includes but not restricted to: •Plant genetics •Animal genetics •Bacterial enzymes •Agricultural Biotechnology, •Biochemistry, •Biophysics, •Bioinformatics, •Environmental Biotechnology, •Industrial Biotechnology, •Microbial biotechnology, •Medical Biotechnology, •Bioenergy, Biosafety, •Biosecurity, •Bioethics, •GMOS, •Genomic, •Proteomic JGEB accepts
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