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. 2017 Nov 7;14(1):216.
doi: 10.1186/s12985-017-0885-3.

Lack of cytomegalovirus detection in human glioma

Affiliations

Lack of cytomegalovirus detection in human glioma

Araceli Garcia-Martinez et al. Virol J. .

Abstract

Gliomas are the most common brain tumors and include a variety of histologic types and grades of malignancy. They arise from glial cells and represent approximately 70% of the primary brain tumors. According to the criteria of the World Health Organization (WHO), the majority of gliomas can be classified into four grades of malignancy (I-IV). Virus infection, especially by DNA viruses and retroviruses, which may cause insertion of viral DNA sequences into the host genome, often triggers the host defense mechanisms. Particularly, the DNA methylation machinery can be activated to cause the methylation of foreign movable viral sequences and, therefore, silence viral gene expression. Several studies have shown the presence of Human Cytomegalovirus (HCMV) in glioblastoma, suggesting that the virus may participate in tumor pathogenesis. But this relationship is controversial because many other studies did not detect HCMV in these tumors. This study aims to detect the presence of HCMV in several samples of human glioma (94 formalin-fixed, paraffin-embedded samples and 28 snap-frozen samples) by different sensitive techniques. We have been unable to detect HCMV DNA and proteins in glioma samples. Therefore, arguments used so far to conclude that HCMV is an oncomodulator virus in gliomas must be, in our view, seriously reconsidered.

Keywords: Detection; Glioma; Gliomagenesis; Human cytomegalovirus.

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Conflict of interest statement

Ethics approval and consent to participate

The study complies with the Declaration of Helsinki and other applicable laws and received approval from the Local Ethics Committee (CEIC Hospital General Universitario de Alicante). All donors provided written informed consent that was freely given.

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

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Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

References

    1. Riemenschneider M. Molecular diagnostics of gliomas: state of the art. Acta Neuropathol. 2010;120(5):567–584. doi: 10.1007/s00401-010-0736-4. - DOI - PMC - PubMed
    1. Ohgaki H, Kleihues P. Genetic alterations and signaling pathways in the evolution of gliomas. Cancer Sci. 2009;100(12):2235–2241. doi: 10.1111/j.1349-7006.2009.01308.x. - DOI - PMC - PubMed
    1. Boeckh M. Complications, diagnosis, management, and prevention of CMV infections: current and future. Hematology Am Soc Hematol Educ Program. 2011;2011:305–309. - PubMed
    1. Mocarski ES, Jr, Kemble GW. Recombinant cytomegaloviruses for study of replication and pathogenesis. Intervirology. 1996;39(5-6):320–330. doi: 10.1159/000150503. - DOI - PubMed
    1. Britt W. Manifestations of human cytomegalovirus infection: proposed mechanisms of acute and chronic disease. Curr Top Microbiol Immunol. 2008;325:417–470. - PubMed