2006
DOI: 10.1002/hep.21092
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A novel function for a micro RNA: Negative regulators can do positive for the hepatitis C virus

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Cited by 10 publications
(6 citation statements)
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“…For example, miRNA may regulate differentiation and maintenance of cell identity in the hematopoietic system (7,8), contribute to establishing muscle phenotypes (9), control morphogenesis of epithelial tissues (10), and regulate aspects of organogenesis (11,12) and metabolic processes (13,14). These structures may also be important in innate immune responses that control viral infections by blocking the synthesis of viral proteins (15). Viral genomes also encode miRNAs and these seem to evolve rapidly, and regulate both the viral life-cycle and the interaction between viruses and their hosts (16).…”
Section: Clinical Relevancementioning
confidence: 99%
“…For example, miRNA may regulate differentiation and maintenance of cell identity in the hematopoietic system (7,8), contribute to establishing muscle phenotypes (9), control morphogenesis of epithelial tissues (10), and regulate aspects of organogenesis (11,12) and metabolic processes (13,14). These structures may also be important in innate immune responses that control viral infections by blocking the synthesis of viral proteins (15). Viral genomes also encode miRNAs and these seem to evolve rapidly, and regulate both the viral life-cycle and the interaction between viruses and their hosts (16).…”
Section: Clinical Relevancementioning
confidence: 99%
“…miR-122 is expressed at high levels in the liver with more than 50,000 copies per cell, where it constitutes 70% of the total miRNA population (47;49;50). Although it was first thought that miRNA acted solely to down-regulate gene expression (51;52), recent results indicate that these small RNA's, in fact, produce both up-and down-regulation of different genes (53)(54)(55). Thus, their effects are multidimensional, and we still have much to learn about their global effects on cells.…”
mentioning
confidence: 99%
“…miR-122 antagomir can inhibit replication of HCV, abundance of HCV core RNA, and expression of HCV nonstructural proteins (NS3 in CNS3 cells and NS3-5B in 9-13 replicon cells), in a time-and dosedependent manner [51,[60][61][62][63]. These findings are suggestive of miR-122 as a potential target for antiviral interventions in HCV patients [37,57,[64][65][66][67].…”
Section: Roles Of Mirnas In Virus-induced Hccmentioning
confidence: 88%