Evidence of BK Polyomavirus Infection in Urothelial but not Renal Tumors from a Single Center Cohort of Kidney Transplant Recipients.
Cinzia BorgognaSilvia AlbertiniLicia MartuscelliFilippo PolettiAlessandro VolpeGuido MerlottiVincenzo CantaluppiRenzo BoldoriniMarisa GariglioPublished in: Viruses (2021)
Emerging evidence indicates that reactivation of BK polyomavirus (BKPyV) in the kidney and urothelial tract of kidney transplant recipients (KTRs) may be associated with cancer in these sites. In this retrospective study of a single center cohort of KTRs (n = 1307), 10 clear cell renal cell carcinomas and 5 urinary bladder carcinomas were analyzed from 15 KTRs for the presence of BKPyV infection through immunohistochemistry and fluorescent in situ hybridization (FISH). Three of these patients had already exhibited biopsy-proven polyomavirus-associated nephropathies (PyVAN). Although the presence of BKPyV large-T antigen was evident in the urothelium from a kidney removed soon after PyVAN diagnosis, it was undetectable in all the formalin-fixed and paraffin-embedded (FFPE) blocks obtained from the 10 kidney tumors. By contrast, large-T antigen (LT) labeling of tumor cells was detected in two out of five bladder carcinomas. Lastly, the proportion of BKPyV DNA-FISH-positive bladder carcinoma nuclei was much lower than that of LT-positive cells. Taken together, our findings further strengthen the association between BKPyV reactivation and cancer development in KTRs, especially bladder carcinoma.
Keyphrases
- high grade
- urinary tract
- papillary thyroid
- spinal cord injury
- end stage renal disease
- squamous cell
- ejection fraction
- induced apoptosis
- newly diagnosed
- chronic kidney disease
- magnetic resonance
- clear cell
- squamous cell carcinoma
- lymph node metastasis
- peritoneal dialysis
- quantum dots
- oxidative stress
- cell cycle arrest
- childhood cancer
- cell therapy
- cell free
- ultrasound guided
- bone marrow
- computed tomography
- mesenchymal stem cells
- young adults
- patient reported outcomes
- cell proliferation
- pi k akt