Lack of presence of the human cytomegalovirus in human glioblastoma

Recent reports have indicated human cytomegalovirus (HCMV) to be associated with human glioblastoma carcinogenesis. In established examples of viral carcinogenesis, viral DNA and one or more of its products have been detected in most tumor cells of biopsies in the majority of cases. To test whether...

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Veröffentlicht in:Modern pathology 2014-07, Vol.27 (7), p.922-929
Hauptverfasser: Yamashita, Yoriko, Ito, Yoshinori, Isomura, Hiroki, Takemura, Naoaki, Okamoto, Akira, Motomura, Kazuya, Tsujiuchi, Takashi, Natsume, Atsushi, Wakabayashi, Toshihiko, Toyokuni, Shinya, Tsurumi, Tatsuya
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container_end_page 929
container_issue 7
container_start_page 922
container_title Modern pathology
container_volume 27
creator Yamashita, Yoriko
Ito, Yoshinori
Isomura, Hiroki
Takemura, Naoaki
Okamoto, Akira
Motomura, Kazuya
Tsujiuchi, Takashi
Natsume, Atsushi
Wakabayashi, Toshihiko
Toyokuni, Shinya
Tsurumi, Tatsuya
description Recent reports have indicated human cytomegalovirus (HCMV) to be associated with human glioblastoma carcinogenesis. In established examples of viral carcinogenesis, viral DNA and one or more of its products have been detected in most tumor cells of biopsies in the majority of cases. To test whether HCMV is associated with human glioblastoma based on this criterion, we measured the number of viral DNA molecules per cell in both frozen and paraffin-embedded tumor biopsies from 58 patients using real-time quantitative PCR (QPCR). Immunohistochemical and fluorescence in situ hybridization (FISH) to detect HCMV proteins and genome was performed in 10 cases using formalin-fixed paraffin-embedded glioblastoma tissues. Southern blotting using DNA extracted from four glioblastoma cell lines together with immunoblotting using the four cell lines and five glioblastoma tissue samples were also performed. We further confirmed the immunoblot bands using liquid chromatography-tandem mass spectrometry assay. As a result, HCMV DNA was not detected in the tumor cells from any of the glioblastoma cases by QPCR detecting two different HCMV genes, in clear contrast to samples from patients with HCMV infection. Southern blotting and immunoblotting of cell lines and FISH using paraffin sections were all negative. However, immunoblotting and immunohistochemistry using tissue samples were partly positive, but HCMV proteins were not detected by proteomic analysis, suggesting false positivity of the analyses. As our QPCR analysis could detect 10 copies of HCMV DNA mixed with DNA extracted from 104 HCMV-negative cells, we conclude that HCMV is not persistent, at least in the tumor cells, of developed human glioblastoma.
doi_str_mv 10.1038/modpathol.2013.219
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subjects 692/699/67/1858
692/699/67/1922
692/700/139/422
Adolescent
Adult
Aged
Aged, 80 and over
Biopsy
Brain Neoplasms - pathology
Brain Neoplasms - virology
Cancer
Child
Chromatography
Cytomegalovirus
Cytomegalovirus - isolation & purification
DNA, Viral - analysis
Female
Genomes
glioblastoma
Glioblastoma - pathology
Glioblastoma - virology
glycoprotein B
Hospitals
Human cytomegalovirus
Humans
immediate early gene
In Situ Hybridization, Fluorescence
Infections
Kinases
Laboratory Medicine
liquid chromatography-tandem mass spectrometry
Male
Mass spectrometry
Medicine
Medicine & Public Health
Middle Aged
original-article
Pathology
Preventive medicine
Proteins
Real-Time Polymerase Chain Reaction
real-time quantitative PCR
Scientific imaging
University graduates
Virology
title Lack of presence of the human cytomegalovirus in human glioblastoma
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