Human herpesvirus multiplex ddPCR detection in brain tissue from low- and high-grade astrocytoma cases and controls
Glioblastoma (GBM) is a fatal CNS malignancy, representing 50 % of all gliomas with approximately 12-18 months survival time after initial diagnosis. Recently, the human herpesvirus cytomegalovirus (CMV) has been suggested to have an oncogenic role, yet this association remains controversial. In add...
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description | Glioblastoma (GBM) is a fatal CNS malignancy, representing 50 % of all gliomas with approximately 12-18 months survival time after initial diagnosis. Recently, the human herpesvirus cytomegalovirus (CMV) has been suggested to have an oncogenic role, yet this association remains controversial. In addition, human herpesvirus 6 (HHV-6) and Epstein-Barr virus (EBV) have also been associated with low-grade gliomas, but few studies have examined HHV-6 and EBV in glioblastomas. Droplet digital PCR (ddPCR) is a highly precise diagnostic tool that enables the absolute quantification of target DNA. This study examines the association between multiple human herpesviruses and astrocytomas.
This study analyzed 112 brain tissue specimens, including 45 glioblastoma, 12 astrocytoma grade III, 2 astrocytoma grade II, 4 astrocytoma grade I, and 49 controls. All brain tissue samples were de-identified and pathologically confirmed. Each tissue block was sectioned for DNA extraction and CMV, EBV, HHV-6A and HHV-6B, and a cellular housekeeping gene were amplified by ddPCR.
Neither CMV nor HHV-6A were detected in any of the astrocytoma samples. However, HHV-6B (p = 0.147) and EBV (p = 0.049) had a higher positivity frequency in the GBM compared to the controls.
The undetectable CMV DNA in the astrocytoma cohort does not support the observation of an increased prevalence of CMV DNA in GBM, as reported in other studies. EBV has a significantly higher positivity in the GBM cohort compared to the controls, while HHV-6B has a higher but not statistically significant positivity in the case cohort. Whether these viruses play an oncogenic role in GBM remains to be further investigated. |
doi_str_mv | 10.1186/s13027-016-0081-x |
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This study analyzed 112 brain tissue specimens, including 45 glioblastoma, 12 astrocytoma grade III, 2 astrocytoma grade II, 4 astrocytoma grade I, and 49 controls. All brain tissue samples were de-identified and pathologically confirmed. Each tissue block was sectioned for DNA extraction and CMV, EBV, HHV-6A and HHV-6B, and a cellular housekeeping gene were amplified by ddPCR.
Neither CMV nor HHV-6A were detected in any of the astrocytoma samples. However, HHV-6B (p = 0.147) and EBV (p = 0.049) had a higher positivity frequency in the GBM compared to the controls.
The undetectable CMV DNA in the astrocytoma cohort does not support the observation of an increased prevalence of CMV DNA in GBM, as reported in other studies. EBV has a significantly higher positivity in the GBM cohort compared to the controls, while HHV-6B has a higher but not statistically significant positivity in the case cohort. Whether these viruses play an oncogenic role in GBM remains to be further investigated.</description><identifier>ISSN: 1750-9378</identifier><identifier>EISSN: 1750-9378</identifier><identifier>DOI: 10.1186/s13027-016-0081-x</identifier><identifier>PMID: 27462365</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject>Brain ; Brain cancer ; Brain research ; Brain tumors ; Care and treatment ; Clinical trials ; Cytomegalovirus ; Cytomegaloviruses ; Deoxyribonucleic acid ; Diagnosis ; Disease control ; DNA ; Genomes ; Gliomas ; Influence ; Lymphoma ; Medical records ; Methods ; Pathogenesis ; Studies ; Tumors ; Viruses</subject><ispartof>Infectious agents and cancer, 2016-07, Vol.11 (1), p.32-32, Article 32</ispartof><rights>COPYRIGHT 2016 BioMed Central Ltd.</rights><rights>Copyright BioMed Central 2016</rights><rights>The Author(s). 2016</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c494t-aeb212d56e89a5b82af1b7c7be0a9e3d80a1383a6c00cf4e0975aa543d000993</citedby><cites>FETCH-LOGICAL-c494t-aeb212d56e89a5b82af1b7c7be0a9e3d80a1383a6c00cf4e0975aa543d000993</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4960850/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4960850/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,27903,27904,53769,53771</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27462365$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lin, Cheng-Te Major</creatorcontrib><creatorcontrib>Leibovitch, Emily C</creatorcontrib><creatorcontrib>Almira-Suarez, M Isabel</creatorcontrib><creatorcontrib>Jacobson, Steven</creatorcontrib><title>Human herpesvirus multiplex ddPCR detection in brain tissue from low- and high-grade astrocytoma cases and controls</title><title>Infectious agents and cancer</title><addtitle>Infect Agent Cancer</addtitle><description>Glioblastoma (GBM) is a fatal CNS malignancy, representing 50 % of all gliomas with approximately 12-18 months survival time after initial diagnosis. Recently, the human herpesvirus cytomegalovirus (CMV) has been suggested to have an oncogenic role, yet this association remains controversial. In addition, human herpesvirus 6 (HHV-6) and Epstein-Barr virus (EBV) have also been associated with low-grade gliomas, but few studies have examined HHV-6 and EBV in glioblastomas. Droplet digital PCR (ddPCR) is a highly precise diagnostic tool that enables the absolute quantification of target DNA. This study examines the association between multiple human herpesviruses and astrocytomas.
This study analyzed 112 brain tissue specimens, including 45 glioblastoma, 12 astrocytoma grade III, 2 astrocytoma grade II, 4 astrocytoma grade I, and 49 controls. All brain tissue samples were de-identified and pathologically confirmed. Each tissue block was sectioned for DNA extraction and CMV, EBV, HHV-6A and HHV-6B, and a cellular housekeeping gene were amplified by ddPCR.
Neither CMV nor HHV-6A were detected in any of the astrocytoma samples. However, HHV-6B (p = 0.147) and EBV (p = 0.049) had a higher positivity frequency in the GBM compared to the controls.
The undetectable CMV DNA in the astrocytoma cohort does not support the observation of an increased prevalence of CMV DNA in GBM, as reported in other studies. EBV has a significantly higher positivity in the GBM cohort compared to the controls, while HHV-6B has a higher but not statistically significant positivity in the case cohort. Whether these viruses play an oncogenic role in GBM remains to be further investigated.</description><subject>Brain</subject><subject>Brain cancer</subject><subject>Brain research</subject><subject>Brain tumors</subject><subject>Care and treatment</subject><subject>Clinical trials</subject><subject>Cytomegalovirus</subject><subject>Cytomegaloviruses</subject><subject>Deoxyribonucleic acid</subject><subject>Diagnosis</subject><subject>Disease control</subject><subject>DNA</subject><subject>Genomes</subject><subject>Gliomas</subject><subject>Influence</subject><subject>Lymphoma</subject><subject>Medical records</subject><subject>Methods</subject><subject>Pathogenesis</subject><subject>Studies</subject><subject>Tumors</subject><subject>Viruses</subject><issn>1750-9378</issn><issn>1750-9378</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><recordid>eNptklFrFDEUhQdRbK3-AF8k4IsvU28mmZnkRSiLWqGgSN_DneTObsrMZE1m2u2_N9uttRUJJOHmO-dywymKtxxOOVfNx8QFVG0JvCkBFC93z4pj3tZQatGq54_uR8WrlK4ApKqUelkcVa1sKtHUx0U6X0ac2IbiltK1j0ti4zLMfjvQjjn3Y_WTOZrJzj5MzE-si5j32ae0EOtjGNkQbkqGk2Mbv96U64iOGKY5Bns7hxGZxUTpDrBhyuUhvS5e9DgkenN_nhSXXz5frs7Li-9fv63OLkortZxLpK7ilasbUhrrTlXY8661bUeAmoRTgFwogY0FsL0k0G2NWEvhAEBrcVJ8Othul24kZyl3x8Fsox8x3pqA3jx9mfzGrMO1kboBVUM2-HBvEMOvhdJsRp8sDQNOFJZkuIK2FrIRPKPv_0GvwhKnPN0dpbkSSv-l1jiQ8VMfcl-7NzVnslFKaVntvU7_Q-XlaPT5D6n3uf5EwA8CG0NKkfqHGTmYfVDMISgmB8Xsg2J2WfPu8ec8KP4kQ_wGqha6SA</recordid><startdate>20160726</startdate><enddate>20160726</enddate><creator>Lin, Cheng-Te Major</creator><creator>Leibovitch, Emily C</creator><creator>Almira-Suarez, M Isabel</creator><creator>Jacobson, Steven</creator><general>BioMed Central Ltd</general><general>BioMed Central</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7TO</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20160726</creationdate><title>Human herpesvirus multiplex ddPCR detection in brain tissue from low- and high-grade astrocytoma cases and controls</title><author>Lin, Cheng-Te Major ; Leibovitch, Emily C ; Almira-Suarez, M Isabel ; Jacobson, Steven</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c494t-aeb212d56e89a5b82af1b7c7be0a9e3d80a1383a6c00cf4e0975aa543d000993</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Brain</topic><topic>Brain cancer</topic><topic>Brain research</topic><topic>Brain tumors</topic><topic>Care and treatment</topic><topic>Clinical trials</topic><topic>Cytomegalovirus</topic><topic>Cytomegaloviruses</topic><topic>Deoxyribonucleic acid</topic><topic>Diagnosis</topic><topic>Disease control</topic><topic>DNA</topic><topic>Genomes</topic><topic>Gliomas</topic><topic>Influence</topic><topic>Lymphoma</topic><topic>Medical records</topic><topic>Methods</topic><topic>Pathogenesis</topic><topic>Studies</topic><topic>Tumors</topic><topic>Viruses</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lin, Cheng-Te Major</creatorcontrib><creatorcontrib>Leibovitch, Emily C</creatorcontrib><creatorcontrib>Almira-Suarez, M Isabel</creatorcontrib><creatorcontrib>Jacobson, Steven</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Infectious agents and cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lin, Cheng-Te Major</au><au>Leibovitch, Emily C</au><au>Almira-Suarez, M Isabel</au><au>Jacobson, Steven</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Human herpesvirus multiplex ddPCR detection in brain tissue from low- and high-grade astrocytoma cases and controls</atitle><jtitle>Infectious agents and cancer</jtitle><addtitle>Infect Agent Cancer</addtitle><date>2016-07-26</date><risdate>2016</risdate><volume>11</volume><issue>1</issue><spage>32</spage><epage>32</epage><pages>32-32</pages><artnum>32</artnum><issn>1750-9378</issn><eissn>1750-9378</eissn><abstract>Glioblastoma (GBM) is a fatal CNS malignancy, representing 50 % of all gliomas with approximately 12-18 months survival time after initial diagnosis. Recently, the human herpesvirus cytomegalovirus (CMV) has been suggested to have an oncogenic role, yet this association remains controversial. In addition, human herpesvirus 6 (HHV-6) and Epstein-Barr virus (EBV) have also been associated with low-grade gliomas, but few studies have examined HHV-6 and EBV in glioblastomas. Droplet digital PCR (ddPCR) is a highly precise diagnostic tool that enables the absolute quantification of target DNA. This study examines the association between multiple human herpesviruses and astrocytomas.
This study analyzed 112 brain tissue specimens, including 45 glioblastoma, 12 astrocytoma grade III, 2 astrocytoma grade II, 4 astrocytoma grade I, and 49 controls. All brain tissue samples were de-identified and pathologically confirmed. Each tissue block was sectioned for DNA extraction and CMV, EBV, HHV-6A and HHV-6B, and a cellular housekeeping gene were amplified by ddPCR.
Neither CMV nor HHV-6A were detected in any of the astrocytoma samples. However, HHV-6B (p = 0.147) and EBV (p = 0.049) had a higher positivity frequency in the GBM compared to the controls.
The undetectable CMV DNA in the astrocytoma cohort does not support the observation of an increased prevalence of CMV DNA in GBM, as reported in other studies. EBV has a significantly higher positivity in the GBM cohort compared to the controls, while HHV-6B has a higher but not statistically significant positivity in the case cohort. Whether these viruses play an oncogenic role in GBM remains to be further investigated.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>27462365</pmid><doi>10.1186/s13027-016-0081-x</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Brain Brain cancer Brain research Brain tumors Care and treatment Clinical trials Cytomegalovirus Cytomegaloviruses Deoxyribonucleic acid Diagnosis Disease control DNA Genomes Gliomas Influence Lymphoma Medical records Methods Pathogenesis Studies Tumors Viruses |
title | Human herpesvirus multiplex ddPCR detection in brain tissue from low- and high-grade astrocytoma cases and controls |
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