Abstract
Around 99% of cervical cancer and 5%–10% of human cancer are associated with human papillomaviruses (HPV). Notably, the life-cycle of HPV begins by low-level infection of the basal cells of the stratified epithelium, where the viral genomes are replicated and passed on to the daughter proliferating basal cells. The production of new viral particles remains restricted to eventually differentiated cells. HPVs support their persistent infectious cycle by hijacking pivotal pathways and cellular processes. Bromodomain-containing protein 4 (BRD4) is one of the essential cellular factors involved in multiple stages of viral transcription and replication. In this review, we demonstrate the role of BRD4 in the multiple stages of HPV infectious cycle. Also, we provide an overview of the intense research about the cellular functions of BRD4, the mechanism of action of bromodomain and extra terminal inhibitors, and how it could lead to the development of antiviral/anticancer therapies.
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CITATION STYLE
Rani, A. Q., Bonam, S. R., Zhou, J., Li, J., Hu, H., & Liu, X. (2023, December 1). BRD4 as a potential target for human papillomaviruses associated cancer. Journal of Medical Virology. John Wiley and Sons Inc. https://doi.org/10.1002/jmv.29294
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