2011
DOI: 10.1016/j.compbiomed.2011.07.007
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Cellular oncomiR orthologue in EBV oncogenesis

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Cited by 19 publications
(20 citation statements)
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“…Together with the fact that the viral miRNA downregulates LTAg, this would then imply that hsa-miR-423-5p negatively regulates this antigenic protein, thereby reducing immune response against the virus and limiting the viral replication rate [64]. Whereas SV40 is the only polyomavirus so far for which this has been demonstrated, the existence of these functional orthologs has also been described for the Human Immunodeficiency Virus-1 (HIV-1) [85], the Herpesviruses Kaposi’s sarcoma-associated herpesvirus and Marek’s Disease Virus [95-98], and Epstein-Barr virus [99]. Although the existence of these functional orthologs appears to be a more general phenomenon, it is not clear whether these host miRNAs really evolved as a mechanism to combat specific viral infections or whether the virus – which likely evolves faster – in fact evolved to mimic specific host miRNAs.…”
Section: Reviewmentioning
confidence: 99%
“…Together with the fact that the viral miRNA downregulates LTAg, this would then imply that hsa-miR-423-5p negatively regulates this antigenic protein, thereby reducing immune response against the virus and limiting the viral replication rate [64]. Whereas SV40 is the only polyomavirus so far for which this has been demonstrated, the existence of these functional orthologs has also been described for the Human Immunodeficiency Virus-1 (HIV-1) [85], the Herpesviruses Kaposi’s sarcoma-associated herpesvirus and Marek’s Disease Virus [95-98], and Epstein-Barr virus [99]. Although the existence of these functional orthologs appears to be a more general phenomenon, it is not clear whether these host miRNAs really evolved as a mechanism to combat specific viral infections or whether the virus – which likely evolves faster – in fact evolved to mimic specific host miRNAs.…”
Section: Reviewmentioning
confidence: 99%
“…Currently, the schemes for targeting miR-BARTs are reviewed in great detail by Lo AK et al [138]. In theory, EBV miRNAs are exogenous genes solely expressed in cancer cells, and display low sequence homology to known human miRNAs [139]. Advantage would be given to the development of miR-BART targeting therapeutic approach because of the tissue specific delivery and the potential off-target effect of the designed bullet.…”
Section: Conclusion and Future Perspectivesmentioning
confidence: 99%
“…For example, EBV-miR-Bam HI-A region rightward transcript (BART)5 and EBV-miR-BART1-3p share similarity with cellular miR-18 (miR-17-92 cluster) and miR-29a/b, respectively. 52,53 Furthermore, viral miRNAs share seed sequence homology among themselves. 50 Moreover, individual EBV miRNAs can target multiple mRNAs, suggesting that many other targets are actually affected and await further identification.…”
Section: Genetic and Mirna Profilementioning
confidence: 99%