跳至主要内容
临床试验/NCT02507882
NCT02507882Unknown不适用

Impact of IL-28B rs12979860 and rs4803217 Gene Polymorphisms Associated With miRNAs Deregulation on HCV-related Hepatocellular Carcinoma

Dr.Waleed Samir1 个研究点 分布在 1 个国家目标入组 405 人开始时间: 2016年1月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
发起方
入组人数
405
试验地点
1
主要终点
IL-28B rs12979860 and rs4803217 Genotype evaluation

研究概览

简要总结

Hepatocellular carcinoma (HCC) is the third leading cause of cancer deaths worldwide as well as in Egypt. Despite improvements in HCC therapy, the prognosis for HCC patients remains poor. Today molecular, genomic and epigenomic aberrations in tumors are being deeply investigated. Many biomarkers were associated to HCC onset, and they could be useful for clinicians, but all show some limitations and no one is so early to predict the HCC onset.

It is estimated that 51.5% of HCC cases can be attributed to HCV infection. Moreover, there is a large occult reservoir of HCV caused chronic liver disease in approximately 9 % in the Egyptian with estimated 6 million HCV chronic infections and estimated 150 000 new infections per year. Among them, we have to mention the polymorphism of IL28B gene rs12979860 C/T. and rs 4803217. The IL-28B gene encodes interferon-lambda 3 (IFN-λ3), which belongs to the type III IFN family. IFN-λ interacts with a transmembrane receptor inducing a potent antiviral response. In experimental model of HCV type III IFN was able to inhibit viral replication. IL-28B polymorphisms are linked to the efficiency of the inflammatory process during HCV infection, and to the mechanisms that HCV adopts to escape by innate and adaptive immunity.

During the last years, a number of studies have assessed the association between the IL-28B polymorphisms and risk of HCC and liver cirrhosis (LC) occurrence in various populations; however, results obtained are still inconclusive.

Interestingly, some polymorphisms located at the 3' untranslated region (UTR) of IL28B, e.g. rs 4803217, seem to interfere with the binding of miRNA, to date recognized as important post-transcriptional regulators. In the last years miRNAs acquired a growing relevance as potential biomarkers for several diseases including cancer, and many researches are focusing on understanding their role in cancer.

Thus the objectives of the current proposal are to determine through investigating a cohort of 405 patients, whether IL28B rs12979860 and rs4803217 polymorphisms are associated to the risk of HCC in chronic hepatitis C (CHC) patients and, above all, to identify their role as predictor marker of HCC in CHC, when associated to miRNAs modulation. Data obtained by our work could be helpful in HCC diagnosis, thus leading to the improvement of the patients prognosis. The proposed activities are going to be implemented through a partnership us as Egyptian Liver Research Institute and Hospital (ELRIAH)- Dakhlya- Egypt and Non- Egyptian Partners.

详细描述

Introduction

Hepatocellular carcinoma (HCC) is the third leading cause of cancer deaths worldwide. Despite improvements in HCC therapy, the prognosis for HCC patients remains poor due to a high incidence of recurrence. An improved understanding of the pathogenesis of HCC development would facilitate the development of more effective outcomes for the diagnosis and treatment of HCC at earlier stages.

Currently, molecular alterations in tumors are being scrutinized at a genome-wide scale, covering different dimensions, such as gene expression, epigenetic changes, chromosomal aberrations, and more recently, next generation sequencing. A large number of molecular markers are associated with the development of HCC. that could be useful in the clinic; however, racial differences have been reported, and these need to be examined more thoroughly.

It is estimated that 51.5% of HCC cases can be attributed to HCV infection. Among them, we have to mention the polymorphisms of IL28B gene, e.g. rs12979860 C/T and rs4803217. The IL-28B gene encodes interferon-lamda 3 (IFN-λ3), which belongs to the type III IFN family including IFN-λ1, IFN-λ2, and IFN-λ3. IFN-λ interacting with a trans membrane receptor induces potent antiviral responses mediated by the activation of the JAK-STAT and MAPK pathways. IL-28B polymorphisms are linked to the efficiency of the inflammatory process during HCV infection and to the mechanisms that HCV adopts to escape by innate and adap¬tive immunity. Interestingly, since type III IFN has been found to inhibit both HBV and HCV replication in experimental models, During the last years, a number of studies have assessed the association between the IL-28B polymorphisms and risk of HCC and liver cirrhosis (LC) development in different populations; however, the results are inconsistent and inconclusive. For these reasons, a deep comprehension of the impact of IL28B polymorphisms in HCC occurrence is mandatory.

Interestingly, some polymorphisms located at the 3' untranslated region (UTR) of IL28B, e.g. rs 4803217, seem to interfere with the binding of miRNA, to date recognized as important post-transcriptional regulators.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
None

入排标准

年龄范围
10 Years 至 —(Child, Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •HCV-infected patients confirmed by RT-PCR with and without fibrosis, cirrhosis and HCC

排除标准

  • •HCV/HIV co-infection

研究组 & 干预措施

HCC

Experimental

This group will include patients with chronic hepatitis C (no. =135)

干预措施: IL28B Polymorphism (Biological)

HCC

Experimental

This group will include patients with chronic hepatitis C (no. =135)

干预措施: miRNA quantification (Biological)

HCC with Cirrhosis

Experimental

This group will include patients with chronic hepatitis C (no. =135) with cirrhosis (F4).

干预措施: IL28B Polymorphism (Biological)

HCC with Cirrhosis

Experimental

This group will include patients with chronic hepatitis C (no. =135) with cirrhosis (F4).

干预措施: miRNA quantification (Biological)

HCV related HCC patients

Experimental

This group will include patients with HCV related HCC (no. =135) This is confirmed by presence of focal lesion detected by Imaging (computed tomography (CT) and ultrasound), and elevated serum AFP.

干预措施: IL28B Polymorphism (Biological)

HCV related HCC patients

Experimental

This group will include patients with HCV related HCC (no. =135) This is confirmed by presence of focal lesion detected by Imaging (computed tomography (CT) and ultrasound), and elevated serum AFP.

干预措施: miRNA quantification (Biological)

结局指标

主要结局

IL-28B rs12979860 and rs4803217 Genotype evaluation

时间窗: 6 months to 1 year from the start of the study

Different types of IL28B and their relation to the progressiveness of HCC

Specific miRNA levels and their association with degree of fibrosis, cirrhosis and HCC

时间窗: 1 to 2 years from the start of the study

次要结局

未报告次要终点

研究者

发起方
Dr.Waleed Samir
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Dr.Waleed Samir

Director of Clinical and Research Laboratory& Head of Molecular Biology Unit, Egyptian Liver Hospital

Egyptian Liver Hospital

研究点 (1)

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