Journal of Clinical Medicine · 2015 · 23 citations · 118 references
Life SciencesGeneticsMolecular BiologyDna ReplicationMolecular VirologyVirologyAntiviral AgentsAntiviral ImmunityDna StabilityViral PathogenesisViral PersistenceViral ReplicationDna Damage Response PathwaysDouble-stranded Dna VirusesHpv PathogenesisPapillomavirus BiologyViral Dna ReplicationViral Genome PersistenceViral Persistence MechanismsViral Replication Control
Most human papillomavirus (HPV) antiviral strategies have focused upon inhibiting viral DNA replication, but it is increasingly apparent that viral DNA levels can be chemically controlled by approaches that promote its instability. HPVs and other DNA viruses have a tenuous relationship with their hosts. They must replicate and hide from the DNA damage response (DDR) and innate immune systems, which serve to protect cells from foreign or "non-self" DNA, and yet they draft these same systems to support their life cycles. DNA binding antiviral agents promoting massive viral DNA instability and elimination are reviewed. Mechanistic studies of these agents have identified genetic antiviral enhancers and repressors, antiviral sensitizers, and host cell elements that protect and stabilize HPV genomes. Viral DNA degradation appears to be an important means of controlling HPV DNA levels in some cases, but the underlying mechanisms remain poorly understood. These findings may prove useful not only for understanding viral DNA persistence but also in devising future antiviral strategies.
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Structure and transcription of human papillomavirus sequences in cervical carcinoma cells
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