A Proteomic Approach to Study the Biological Role of Hepatitis C Virus Protein Core+1/ARFP

被引:3
|
作者
Vrazas, Vasileios [1 ]
Moustafa, Savvina [2 ]
Makridakis, Manousos [3 ]
Karakasiliotis, Ioannis [4 ]
Vlahou, Antonia [3 ]
Mavromara, Penelope [1 ]
Katsani, Katerina R. [1 ]
机构
[1] Democritus Univ Thrace, Dept Mol Biol & Genet, Lab Biochem & Mol Virol, Alexandroupolis 68100, Greece
[2] Hippokrat Gen Hosp Athens, Dept Med & Lab 2, Clin Immunol Rheumatol Unit, Athens 11527, Greece
[3] Acad Athens, Biomed Res Fdn, Ctr Basic Res, Athens 11527, Greece
[4] Democritus Univ Thrace, Dept Med, Lab Biol, Alexandroupolis 68100, Greece
来源
VIRUSES-BASEL | 2022年 / 14卷 / 08期
关键词
proteomics; HCV-1a; Core+1; ARFP; Huh7; 5; liver diseases; READING FRAME PROTEIN; F-PROTEIN; HCV-ARF/CORE+1 PROTEIN; RNA REPLICATION; EXPRESSION; CORE; HCV; TRANSLATION; MECHANISMS; ANTIBODIES;
D O I
10.3390/v14081694
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Hepatitis C virus is the major cause of chronic liver diseases and the only cytoplasmic RNA virus known to be oncogenic in humans. The viral genome gives rise to ten mature proteins and to additional proteins, which are the products of alternative translation initiation mechanisms. A protein-known as ARFP (alternative reading frame protein) or Core+1 protein-is synthesized by an open reading frame overlapping the HCV Core coding region in the (+1) frame of genotype 1a. Almost 20 years after its discovery, we still know little of the biological role of the ARFP/Core+1 protein. Here, our differential proteomic analysis of stable hepatoma cell lines expressing the Core+1/Long isoform of HCV-1a relates the expression of the Core+1/Long isoform with the progression of the pathology of HCV liver disease to cancer.
引用
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页数:17
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