Epstein–Barr Virus in Brain Cancer—Friend or Foe?

Recent research suggests a link between EBV and brain cancer, especially in high-grade gliomas, but its role has not been sufficiently elucidated. Therefore, we evaluated its occurrence in brain cancer. For this purpose, the EBV DNA and LMP-1 in tumor tissue, the level of viral load in the cerebrospinal fluid (CSF), and the serological status of patients were analyzed. We detected EBV DNA in 28.9% (42/145) of glioma samples, among which 28 were isolated from glioblastomas (GBs) and 14 from other gliomas. LMP-1 was detected in 26 (92.8%) GB samples and 5 (35.7%) samples from other gliomas. The EBV DNA load in the CSF was significantly higher in GB compared to other gliomas; anti-EBNA1, anti-EBVCA, anti-EA, and anti-Zta antibodies were detected in the serum of GB patients; and their concentration was higher in GB patients. Further research is needed to determine whether and to what extent EBV contributes to glioma development. Elucidating the role of latent EBV genes synthesized in glioblastoma is important for understanding the role of viral infection in cancer development and progression in this hitherto poorly studied area.

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Publication Details

Journal
International Journal of Molecular Sciences
Published
2026-05-27
DOI
https://doi.org/10.3390/ijms27114812
Primary Topic
Viral-associated cancers and disorders
Type
article
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article

Epstein–Barr Virus in Brain Cancer—Friend or Foe?

Magdalena Góralczyk, Sylwester Bogacki, Michał Brzozowski, Małgorzata Polz-Dacewicz
International Journal of Molecular Sciences
Viral-associated cancers and disorders
article

Epstein–Barr Virus in Brain Cancer—Friend or Foe?

Magdalena Góralczyk, Sylwester Bogacki, Michał Brzozowski, Małgorzata Polz-Dacewicz
article en

Abstract

Recent research suggests a link between EBV and brain cancer, especially in high-grade gliomas, but its role has not been sufficiently elucidated. Therefore, we evaluated its occurrence in brain cancer. For this purpose, the EBV DNA and LMP-1 in tumor tissue, the level of viral load in the cerebrospinal fluid (CSF), and the serological status of patients were analyzed. We detected EBV DNA in 28.9% (42/145) of glioma samples, among which 28 were isolated from glioblastomas (GBs) and 14 from other gliomas. LMP-1 was detected in 26 (92.8%) GB samples and 5 (35.7%) samples from other gliomas. The EBV DNA load in the CSF was significantly higher in GB compared to other gliomas; anti-EBNA1, anti-EBVCA, anti-EA, and anti-Zta antibodies were detected in the serum of GB patients; and their concentration was higher in GB patients. Further research is needed to determine whether and to what extent EBV contributes to glioma development. Elucidating the role of latent EBV genes synthesized in glioblastoma is important for understanding the role of viral infection in cancer development and progression in this hitherto poorly studied area.

International Journal of Molecular SciencesVol. 27(11)
Medical University of Lublin (PL), University of Economics and Innovation (PL), 1 Military Clinical Hospital with Outpatient Clinic (PL)
Good health and well-being
Openalex Percentile: Top 12%
Viral-associated cancers and disorders
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