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 |
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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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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.</description><identifier>ISSN: 0893-3952</identifier><identifier>EISSN: 1530-0285</identifier><identifier>DOI: 10.1038/modpathol.2013.219</identifier><identifier>PMID: 24336154</identifier><identifier>CODEN: MODPEO</identifier><language>eng</language><publisher>New York: Elsevier Inc</publisher><subject>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</subject><ispartof>Modern pathology, 2014-07, Vol.27 (7), p.922-929</ispartof><rights>2014 United States & Canadian Academy of Pathology</rights><rights>United States & Canadian Academy of Pathology 2014</rights><rights>Copyright Nature Publishing Group Jul 2014</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c641t-c6485613825220acded22d72803e61582333064c5ddc42a508e67534731f5dd53</citedby><cites>FETCH-LOGICAL-c641t-c6485613825220acded22d72803e61582333064c5ddc42a508e67534731f5dd53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24336154$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yamashita, Yoriko</creatorcontrib><creatorcontrib>Ito, Yoshinori</creatorcontrib><creatorcontrib>Isomura, Hiroki</creatorcontrib><creatorcontrib>Takemura, Naoaki</creatorcontrib><creatorcontrib>Okamoto, Akira</creatorcontrib><creatorcontrib>Motomura, Kazuya</creatorcontrib><creatorcontrib>Tsujiuchi, Takashi</creatorcontrib><creatorcontrib>Natsume, Atsushi</creatorcontrib><creatorcontrib>Wakabayashi, Toshihiko</creatorcontrib><creatorcontrib>Toyokuni, Shinya</creatorcontrib><creatorcontrib>Tsurumi, Tatsuya</creatorcontrib><title>Lack of presence of the human cytomegalovirus in human glioblastoma</title><title>Modern pathology</title><addtitle>Mod Pathol</addtitle><addtitle>Mod Pathol</addtitle><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.</description><subject>692/699/67/1858</subject><subject>692/699/67/1922</subject><subject>692/700/139/422</subject><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Biopsy</subject><subject>Brain Neoplasms - pathology</subject><subject>Brain Neoplasms - virology</subject><subject>Cancer</subject><subject>Child</subject><subject>Chromatography</subject><subject>Cytomegalovirus</subject><subject>Cytomegalovirus - isolation & purification</subject><subject>DNA, Viral - analysis</subject><subject>Female</subject><subject>Genomes</subject><subject>glioblastoma</subject><subject>Glioblastoma - pathology</subject><subject>Glioblastoma - virology</subject><subject>glycoprotein 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Kazuya</au><au>Tsujiuchi, Takashi</au><au>Natsume, Atsushi</au><au>Wakabayashi, Toshihiko</au><au>Toyokuni, Shinya</au><au>Tsurumi, Tatsuya</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Lack of presence of the human cytomegalovirus in human glioblastoma</atitle><jtitle>Modern pathology</jtitle><stitle>Mod Pathol</stitle><addtitle>Mod Pathol</addtitle><date>2014-07-01</date><risdate>2014</risdate><volume>27</volume><issue>7</issue><spage>922</spage><epage>929</epage><pages>922-929</pages><issn>0893-3952</issn><eissn>1530-0285</eissn><coden>MODPEO</coden><abstract>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.</abstract><cop>New York</cop><pub>Elsevier Inc</pub><pmid>24336154</pmid><doi>10.1038/modpathol.2013.219</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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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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