Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2020 Sep 14;17(1):139.
doi: 10.1186/s12985-020-01399-7.

BK polyomavirus infection promotes growth and aggressiveness in bladder cancer

Affiliations

BK polyomavirus infection promotes growth and aggressiveness in bladder cancer

Yigang Zeng et al. Virol J. .

Abstract

Background: Recent studies have confirmed the integration of the BK polyomavirus (BKPyV) gene into the cellular genome of urothelial carcinomas in transplant recipients, further confirming the correlation between BKPyV and urothelial carcinomas after transplantation. However, the role BKPyV infections play in the biological function of bladder cancer remains unclear.

Methods: We developed a BKPyV-infected bladder cancer cell model and a mice tumor model to discuss the role of BKPyV infections.

Results: Our research proves that BKPyV infections promote the proliferation, invasion and migration of bladder cancer cells, while the activation of β-catenin signaling pathway is one of its mediation mechanisms.

Conclusions: We first described BKPyV infection promotes the proliferation, invasion and migration of bladder cancer. We verified the role of β-catenin signaling pathway and Epithelial-Mesenchymal Transition effect in BKPyV-infected bladder cancer. These results provide meaningful information towards the diagnosis and treatment of clinical bladder cancer.

Keywords: BK polyomavirus; Bladder cancer; Cell aggressiveness; Cell growth.

PubMed Disclaimer

Conflict of interest statement

The authors declare that they have no competing interests.

Figures

Fig. 1
Fig. 1
BKPyV infection in bladder cancer cells is a non-lytic infection (MOI 2; 48 h post infection). a Immunofluorescence staining was performed (red: LTag, blue, DNA, and images were taken at 400× magnification). b, c BKPyV infection significantly increased growth in T24 and HTB-9 cells, as measured by CCK-8. The effect was significantly reversed by KYA1797K. All graphs represent the mean ± SD obtained from three independent experiments. *P < 0.05, **P < 0.01, ***P < 0.001; + BKV versus control; + BKV + KYA1797K versus + BKV; Student’s t-test or one-way ANOVA
Fig. 2
Fig. 2
BKPyV infection promotes proliferation, invasion and migration of bladder cancer cells. a, b BKPyV infection significantly increased growth in T24 and HTB-9 cells, as measured by colony formation. ch BKPyV infection significantly promoted migration of T24 and HTB-9 cells, as measured by the Transwell migration assay (c, d) and wound healing assay (eh) after infected with BKPyV 48 h. i, j Transwell invasion assay showed that BKPyV infection significantly promoted invasiveness of T24 and HTB-9 cells. These effect was significantly reversed by KYA1797K. All images were taken at 100× magnification. All graphs represent the mean ± SD obtained from three independent experiments. *P < 0.05, **P < 0.01, ***P < 0.001; + BKV versus control; + BKV + KYA1797K versus + BKV; Student’s t-test or one-way ANOVA
Fig. 3
Fig. 3
BKPyV infection enhances bladder tumor growth and metastasis. a T24, HTB-9 and their respective BKPyV-infected cells were injected subcutaneously into nude mice with subsequent intraperitoneal injection of KYA1797K (20 mg/kg) (n = 5). Tumor volumes (b, c) of mice were measured every 5 days. BKPyV infection significantly promoted tumor growth in vivo. The effect was significantly reversed by KYA1797K. Tumors were subjected to H&E staining (d) (200×) and TUNEL immunohistochemistry (e, f) (200×). TUNEL staining showed that BKPyV infection significantly induced tumor apoptosis. The effect was significantly reversed by KYA1797K. g Representative images of liver, metastatic nodules (indicated by arrows) are shown. h Livers were subjected to H&E staining (original magnification,40×; smaller image at lower left, 200×). Liver metastasis was found only in the BKPyV-infected group. The effect was significantly reversed by KYA1797K. All graphs represent the mean ± SD obtained from three independent experiments. *P < 0.05, **P < 0.01, ***P < 0.001; + BKPyV versus control; + BKPyV +KYA1797K versus + BKPyV; Student’s t-test or one-way ANOVA
Fig. 4
Fig. 4
BKPyV infection enhances β-catenin signaling pathway activation and EMT effect in bladder cancer cells. a-f Expression levels of β-catenin, cMYC, and EMT-related proteins investigated by western blotting. β-Actin was used as a loading control. The effect was significantly reversed by β-catenin inhibitor (KYA1797K). All graphs represent the mean ± SD obtained from three independent experiments. *P < 0.05, **P < 0.01, ***P < 0.001; + BKPyV versus control; + BKPyV +KYA1797K versus + BKPyV; Student’s t-test or one-way ANOVA

Similar articles

Cited by

References

    1. Bray F, Ferlay J, Soerjomataram I, Siegel RL, Torre LA, Jemal A. Global cancer statistics 2018: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA Cancer J Clin. 2018;68(6):394–424. - PubMed
    1. Gaughan KP, Haroon U, Davis NF, Mohan P. Urothelial carcinoma of an allograft ureter 10 years after deceased donor kidney transplantation. BMJ Case Rep. 2018;2018:bcr2017223087. - PMC - PubMed
    1. Hickman LA, Sawinski D, Guzzo T, Locke JE. Urologic malignancies in kidney transplantation. Am J Transplant. 2018;18(1):13–22. - PubMed
    1. Erard V, Storer B, Corey L, Nollkamper J, Huang ML, Limaye A, Boeckh M. BK virus infection in hematopoietic stem cell transplant recipients: frequency, risk factors, and association with postengraftment hemorrhagic cystitis. Clin Infect Dis. 2004;39(12):1861–1865. - PubMed
    1. Bouvard V, Baan RA, Grosse Y, Lauby-Secretan B, El Ghissassi F, Benbrahim-Tallaa L, Guha N, Straif K, Group WHOIAfRoCMW Carcinogenicity of malaria and of some polyomaviruses. Lancet Oncol. 2012;13(4):339–340. - PubMed

Publication types

MeSH terms