1. BK polyomavirus (BKPyV) is a risk factor for bladder cancer through induction of APOBEC3-mediated genomic damage
- Author
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Jennifer Southgate, Reuben S. Harris, Slip Rg, Simon C. Baker, Skinner Kt, Manikandan Periyasamy, Tim R. Fenton, Masood O, Simak Ali, Andrew S. Mason, and Andrew Macdonald
- Subjects
Kidney ,Bladder cancer ,biology ,business.industry ,EZH2 ,Retinoblastoma protein ,Cell cycle ,medicine.disease ,medicine.anatomical_structure ,Cancer research ,medicine ,biology.protein ,FOXM1 ,E2F1 ,APOBEC3A ,business - Abstract
Limited understanding of bladder cancer aetiopathology hampers progress in reducing incidence. BK polyomavirus (BKPyV) is a common childhood infection that can be reactivated in the adult kidney leading to viruria. Here we used a mitotically-quiescent, differentiated, normal human urothelial in vitro model to study BKPyV infection. BKPyV infection led to significantly elevated APOBEC3A and APOBEC3B protein, increased deaminase activity and greater numbers of apurinic/apyrimidinic sites in the host urothelial genome. BKPyV Large T antigen (LT-Ag) stimulated re-entry into the cell cycle via inhibition of Retinoblastoma protein and activation of EZH2, E2F1 and FOXM1, which combined to push urothelial cells from G0 into an arrested G2 cell cycle state. The single-stranded DNA displacement loops formed during BKPyV-infection, provide a substrate for APOBEC3 enzymes where they interacted with LT-Ag. These results support reactivated BKPyV infections in adults as a risk factor for bladder cancer in immune-insufficient populations, including transplant patients and the elderly.
- Published
- 2021
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