Promising Targets for Anti-Hepatitis C Virus Agents

被引:8
|
作者
Yoshida, T. [1 ]
Kondoh, M. [1 ]
Yagi, K. [1 ]
机构
[1] Osaka Univ, Grad Sch Pharmaceut Sci, Lab Biofunct Mol Chem, Suita, Osaka 5650871, Japan
关键词
Hepatitis C virus; CD81; claudin-1; NS3; helicase; cyclophilin; miRNA122; INTERNAL RIBOSOMAL ENTRY; PLACEBO-CONTROLLED TRIAL; P7; ION-CHANNEL; HELICASE ACTIVITY; BINDING-PROTEIN; RNA HELICASE; ANTIVIRAL ACTIVITY; INITIAL TREATMENT; POTENT INHIBITOR; NS4A ANTAGONIST;
D O I
10.2174/092986711795029672
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Hepatitis C virus (HCV) infection is a serious global health problem, with 3-4 million new cases reported each year. Chronic HCV infection places 170 million people at risk of developing liver cirrhosis and hepatocellular carcinoma. However, difficulties in preparing HCV particles in vitro have delayed development of effective anti-HCV therapies. In 2005, Wakita et al. developed an in vitro method to prepare HCV particles, thereby enabling researchers to better understand the mechanism of HCV infection. Other recent advances include development of a virus-free system for evaluating HCV replication and the identification of HCV receptors, such as claudin-1 and occludin, that may serve as targets for anti-HCV drugs. In this review, we discuss recent findings in HCV infection research, including discovery of new potential targets for anti-HCV therapy.
引用
收藏
页码:1239 / 1244
页数:6
相关论文
共 50 条
  • [41] Seronegative anti-hepatitis C virus antibody in hemodialysis patients
    Alavian, Seyyed Moayed
    HEMODIALYSIS INTERNATIONAL, 2013, 17 (02) : 328 - 328
  • [42] Potent inhibitors of hepatitis C core dimerization as new leads for anti-hepatitis C agents
    Ni, Feng
    Kota, Smitha
    Takahashi, Virginia
    Strosberg, A. Donny
    Snyder, John K.
    BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2011, 21 (08) : 2198 - 2202
  • [43] A Quantitative Structure-Activity Relationship Study on a Few Series of Anti-hepatitis C Virus Agents
    Varshney, Jonish
    Sharma, Anjana
    Gupta, Satya P.
    MEDICINAL CHEMISTRY, 2012, 8 (03) : 491 - 504
  • [44] Synthesis of novel diflunisal hydrazide hydrazones as anti-hepatitis C virus agents and hepatocellular carcinoma inhibitors
    Senkardes, Sevil
    Kaushik-Basu, Neerja
    Durmaz, Irem
    Manvar, Dinesh
    Basu, Amartya
    Atalay, Rengul
    Kucukguzel, S. Guniz
    EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2016, 108 : 301 - 308
  • [45] Flavonoid-triazolyl hybrids as potential anti-hepatitis C virus agents: Synthesis and biological evaluation
    Zhang, Han
    Zheng, Xin
    Li, Jichong
    Liu, Qingbo
    Huang, Xiao-Xiao
    Ding, Huaiwei
    Suzuki, Ryosuke
    Muramatsu, Masamichi
    Song, Shao-Jiang
    EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2021, 218
  • [46] A QSAR study on some series of anti-hepatitis B virus (HBV) agents
    Arora, Preet K.
    Patil, Vaishali M.
    Gupta, Satya P.
    BIOINFORMATION, 2010, 4 (09) : 417 - 420
  • [47] Synthesis and the biological evaluation of arylnaphthalene lignans as anti-hepatitis B virus agents
    Janmanchi, Damodar
    Tseng, Ya Ping
    Wang, Kuei-Chen
    Huang, Ray Ling
    Lin, Chih Hsiu
    Yeh, Sheau Farn
    BIOORGANIC & MEDICINAL CHEMISTRY, 2010, 18 (03) : 1213 - 1226
  • [48] Synthesis and the Biological Evaluation of Arylnaphthalene Lignans as Anti-hepatitis B Virus Agents
    Yeh, Sheau Farn
    Lin, Chih Hsiu
    Janmanchi, Damodar
    Tseng, Ya Ping
    FASEB JOURNAL, 2010, 24
  • [49] Low prevalence of hepatitis C virus RNA in blood donors with anti-hepatitis C virus reactivity in Rwanda
    Twagirumugabe, Theogene
    Swaibu, Gatare
    Bergstrom, Tomas
    Walker, Timothy David
    Gahutu, Jean Bosco
    Norder, Helene
    TRANSFUSION, 2017, 57 (10) : 2420 - 2432
  • [50] Chemical genetics approach to hepatitis C virus replication: cyclophilin as a target for anti-hepatitis C virus strategy
    Watashi, Koichi
    Shimotohno, Kunitada
    REVIEWS IN MEDICAL VIROLOGY, 2007, 17 (04) : 245 - 252