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Related Concept Videos

Rous Sarcoma Virus (RSV) and Cancer01:03

Rous Sarcoma Virus (RSV) and Cancer

Rous Sarcoma virus or RSV was discovered by F. Peyton Rous in the year 1911 as a filterable transmissible agent that could cause tumors in chickens. He won a Nobel Prize for this discovery in 1966. His experiments clearly demonstrated that some cancers could be caused by infectious agents and led to the discovery of many more cancer-causing viruses in animals as well as humans.
RSV is a retrovirus that contains two copies of a plus-strand  RNA genome. Its genome consists of four main open...
Rous Sarcoma Virus (RSV) and Cancer01:03

Rous Sarcoma Virus (RSV) and Cancer

Rous Sarcoma virus or RSV was discovered by F. Peyton Rous in the year 1911 as a filterable transmissible agent that could cause tumors in chickens. He won a Nobel Prize for this discovery in 1966. His experiments clearly demonstrated that some cancers could be caused by infectious agents and led to the discovery of many more cancer-causing viruses in animals as well as humans.
RSV is a retrovirus that contains two copies of a plus-strand  RNA genome. Its genome consists of four main open...
The Tumor Microenvironment02:17

The Tumor Microenvironment

Every normal cell or tissue is embedded in a complex local environment called stroma, consisting of different cell types, a basal membrane, and blood vessels. As normal cells mutate and develop into cancer cells, their local environment also changes to allow cancer progression. The tumor microenvironment (TME) consists of a complex cellular matrix of stromal cells and the developing tumor. The cross-talk between cancer cells and surrounding stromal cells is critical to disrupt normal tissue...
The Tumor Microenvironment02:17

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Arboviral Encephalitis01:25

Arboviral Encephalitis

Arboviral encephalitis refers to brain inflammation caused by arthropod-borne viruses, particularly those transmitted through mosquito vectors. Among these, West Nile virus (WNV), a member of the Flaviviridae family, is a significant public health concern. WNV is an enveloped, positive-sense, single-stranded RNA virus. Human infection typically begins when an infected mosquito introduces the virus into the dermis during feeding. The primary transmission cycle involves birds as amplifying hosts...
Encephalitis l: Introduction01:19

Encephalitis l: Introduction

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Related Experiment Video

Updated: Jun 13, 2026

Isolation and Quantification of Epstein-Barr Virus from the P3HR1 Cell Line
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Published on: September 28, 2022

Epstein-Barr Virus in Brain Cancer-Friend or Foe?

Michał Brzozowski1, Magdalena Góralczyk2, Sylwester Bogacki3

  • 1Neurosurgery Department, 1st Clinical Military Hospital with Outpatient Clinic in Lublin, 20-049 Lublin, Poland.

International Journal of Molecular Sciences
|June 12, 2026
PubMed
Summary

Epstein-Barr virus (EBV) DNA and proteins were found in brain tumors, particularly glioblastomas (GBs). Higher viral loads and antibodies in GB patients suggest EBV may play a role in glioma development.

Keywords:
EBVbrain cancerglioblastoma

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Published on: September 7, 2022

Area of Science:

  • Neuro-oncology
  • Viral oncology
  • Molecular biology

Background:

  • Epstein-Barr virus (EBV) is linked to various cancers.
  • Its specific role in brain cancers, especially high-grade gliomas, remains unclear.
  • Understanding EBV's contribution to glioma pathogenesis is crucial.

Purpose of the Study:

  • To investigate the prevalence and role of Epstein-Barr virus (EBV) in brain cancer.
  • To analyze EBV DNA, LMP-1 expression, viral load in CSF, and serological status in glioma patients.

Main Methods:

  • Analysis of EBV DNA and LMP-1 in 145 glioma tumor tissues.
  • Quantification of EBV DNA load in cerebrospinal fluid (CSF).
  • Detection of EBV-specific antibodies (anti-EBNA1, anti-EBVCA, anti-EA, anti-Zta) in patient serum.

Main Results:

  • EBV DNA detected in 28.9% of glioma samples (42/145), with higher prevalence in glioblastomas (GBs).
  • LMP-1 expression was significantly higher in GBs (92.8%) compared to other gliomas (35.7%).
  • GB patients showed significantly higher EBV DNA loads in CSF and elevated levels of EBV-specific antibodies.

Conclusions:

  • The findings indicate a significant association between EBV and high-grade gliomas, particularly glioblastomas.
  • Further research is necessary to elucidate the extent of EBV's contribution to glioma development and progression.
  • Investigating latent EBV genes in glioblastoma is vital for understanding viral infection's role in cancer.