Virus-induced APOBEC3 transmutagenesis in bladder cancer initiation

Carcinogenesis in human urothelium is driven by a high burden of mutations caused by the antiviral "APOBEC3" (apolipoprotein B mRNA editing enzyme, catalytic subunit-like 3) cytosine deaminase enzymes; however, there is no established viral etiology. BK polyomavirus (BKPyV) is a ubiquitous childhood infection that persists in the kidney during adulthood and is frequently detected in urine. Chronic BKPyV infections of normal human urothelium induced an innate response, including apical extrusion of infected cells. Local paracrine interferon signaling induced APOBEC3 expression in both infected and juxtaposed bystander cells, leading to acquisition of hallmark APOBEC3-mediated mutational signatures that recapitulated the variation in mutational character found in patients with muscle-invasive bladder cancer. In our model for urothelial carcinogenesis, uninfected bystander cells witnessing BKPyV infection become APOBEC3 damaged, escape extrusion, and acquire hypermutable advantage. "Transmutagenesis" explains how cells proximal to infected neighbors acquire cancer-initiating mutations. This hypothesis for how urothelial cancers can develop as APOBEC3 signature rich, while remaining virus-negative, suggests that a large proportion of urothelial carcinomas may be preventable by antiviral intervention.

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Publication Details

Journal
Science Advances
Published
2025-12-03
DOI
https://doi.org/10.1126/sciadv.aea6124
Citations
2
Primary Topic
Polyomavirus and related diseases
Type
article
Field-Weighted Citation Impact
2.09
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article

Virus-induced APOBEC3 transmutagenesis in bladder cancer initiation

Sally James, Matthew Welberry Smith, Gabriel J. Starrett, Helena Vogel et al.
2 citations
Science Advances
Polyomavirus and related diseases
2.09
article

Virus-induced APOBEC3 transmutagenesis in bladder cancer initiation

Sally James, Matthew Welberry Smith, Gabriel J. Starrett, Helena Vogel, Iñigo Martincorena, Jennifer Southgate, Reuben S. Harris, Anjum Bashir Khan, Andrew Macdonald, Karen Hogg, Andrew S. Mason, Michael A. Carpenter, Grace B. Hatton, Gemma Swinscoe, Richard T. Gawne, Simon C. Baker, Omar Masood, Parisa Boukani
article en
2 citations

Abstract

Carcinogenesis in human urothelium is driven by a high burden of mutations caused by the antiviral "APOBEC3" (apolipoprotein B mRNA editing enzyme, catalytic subunit-like 3) cytosine deaminase enzymes; however, there is no established viral etiology. BK polyomavirus (BKPyV) is a ubiquitous childhood infection that persists in the kidney during adulthood and is frequently detected in urine. Chronic BKPyV infections of normal human urothelium induced an innate response, including apical extrusion of infected cells. Local paracrine interferon signaling induced APOBEC3 expression in both infected and juxtaposed bystander cells, leading to acquisition of hallmark APOBEC3-mediated mutational signatures that recapitulated the variation in mutational character found in patients with muscle-invasive bladder cancer. In our model for urothelial carcinogenesis, uninfected bystander cells witnessing BKPyV infection become APOBEC3 damaged, escape extrusion, and acquire hypermutable advantage. "Transmutagenesis" explains how cells proximal to infected neighbors acquire cancer-initiating mutations. This hypothesis for how urothelial cancers can develop as APOBEC3 signature rich, while remaining virus-negative, suggests that a large proportion of urothelial carcinomas may be preventable by antiviral intervention.

Science AdvancesVol. 11(49)
National Institutes of Health (US), University of Leeds (GB), Howard Hughes Medical Institute (US), Leeds Teaching Hospitals NHS Trust (GB), St James's University Hospital (GB), Wellcome Sanger Institute (GB), National Cancer Institute (US), Center for Cancer Research (US), The University of Texas at San Antonio (US), University of York (GB)
Openalex Percentile: Top 10%
Polyomavirus and related diseases
2.09
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