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Recent Insights into the Control of Human Papillomavirus (HPV) Genome Stability, Loss, and Degradation

Journal

JOURNAL OF CLINICAL MEDICINE
Volume 4, Issue 2, Pages 204-230

Publisher

MDPI
DOI: 10.3390/jcm4020204

Keywords

HPV; antiviral; polyamide; antiviral sensitizer; MRE11; viral persistence; TDP1; TDP2; RTEL1; RUVBL2

Funding

  1. NIAID NIH HHS [R41 AI062182, R41 AI068159, R42 AI062182, R42 AI068159] Funding Source: Medline

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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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