Evidence of association of human papillomavirus with prognosis worsening in glioblastoma multiforme
Glioblastoma multiforme (GBM) is the most malignant brain tumor in adults, but its etiology still remains unknown. Recently, a role of viruses such as cytomegalovirus and JC virus in gliomagenesis has been suggested. Since human papillomavirus (HPV) is considered the most common oncogenic virus in h...
Gespeichert in:
Veröffentlicht in: | Neuro-oncology (Charlottesville, Va.) Va.), 2014-01, Vol.16 (2), p.298-302 |
---|---|
Hauptverfasser: | , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 302 |
---|---|
container_issue | 2 |
container_start_page | 298 |
container_title | Neuro-oncology (Charlottesville, Va.) |
container_volume | 16 |
creator | Vidone, Michele Alessandrini, Federica Marucci, Gianluca Farnedi, Anna de Biase, Dario Ricceri, Fulvio Calabrese, Claudia Kurelac, Ivana Porcelli, Anna Maria Cricca, Monica Gasparre, Giuseppe |
description | Glioblastoma multiforme (GBM) is the most malignant brain tumor in adults, but its etiology still remains unknown. Recently, a role of viruses such as cytomegalovirus and JC virus in gliomagenesis has been suggested. Since human papillomavirus (HPV) is considered the most common oncogenic virus in humans, we evaluated its occurrence in GBM samples.
Fifty-two formalin-fixed paraffin-embedded primary glioblastoma specimens were retrospectively analyzed. The presence of HPV genome on tumor DNA was assessed by MY/GP nested PCR. Confirmation of HPV detection was obtained by chromogenic in situ hybridization (CISH) and immunohistochemistry (IHC) with an antibody directed against the L1 capsidic protein. Finally, univariate and multivariate proportional-hazards models were used to compare the risk of death among HPV-positive and HPV-negative patients.
Strikingly, viral DNA was detected after PCR in 12 cases (23%). HPV16 genome was present in 25% infected samples, whereas the remaining samples tested positive for HPV6. CISH confirmed positivity in all infected samples for which enough material was available. Moreover, IHC positivity suggested that production of viral proteins from HPV genome is an ongoing process in GBM cancer cells. Finally an association between HPV infection and a worse prognosis was found in patients upon age stratification with a univariate analysis (HR, 2.10; 95% CI, 1.00-4.44; log-rank P = .045).
HPV infection status may be considered an independent prognostic factor in GBM patients and suggests that prevention may be considered, should HPV be recognized as a causative agent in gliomagenesis. |
doi_str_mv | 10.1093/neuonc/not140 |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3895373</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1490901199</sourcerecordid><originalsourceid>FETCH-LOGICAL-c387t-e9835b5eb61b705e1b6dc2965144ba50e853b2af97a59b5d6b8d1481db3062cd3</originalsourceid><addsrcrecordid>eNpVkU1LxDAQhoMo7rp69Co9eqmbNE2bXARZ1g9Y8KLnkKRpN5ImNWlX_Pd27Sp6mhnm4Z2BB4BLBG8QZHjp9OCdWjrfoxwegTkiGU4JLYrj7z5LKUHlDJzF-AZhhkiBTsEsyzNKSM7mQK13ptJO6cTXiYjRKyN6491-3A6tcEknOmOtb8XOhCEmH6bfJl3wjfPRjKMPUTvjmsS4pLHGSytiP9JJO9je1D60-hyc1MJGfXGoC_B6v35ZPaab54en1d0mVZiWfaoZxUQSLQskS0g0kkWlMlYQlOdSEKgpwTITNSsFYZJUhaQVyimqJIZFpiq8ALdTbjfIVldKuz4Iy7tgWhE-uReG_984s-WN33FMGcElHgOuDwHBvw869rw1UWlrhdN-iBzlDDKIEGMjmk6oCj7GoOvfMwjyvRg-ieGTmJG_-vvbL_1jAn8Be26PyQ</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1490901199</pqid></control><display><type>article</type><title>Evidence of association of human papillomavirus with prognosis worsening in glioblastoma multiforme</title><source>MEDLINE</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>Oxford University Press Journals All Titles (1996-Current)</source><source>PubMed Central</source><creator>Vidone, Michele ; Alessandrini, Federica ; Marucci, Gianluca ; Farnedi, Anna ; de Biase, Dario ; Ricceri, Fulvio ; Calabrese, Claudia ; Kurelac, Ivana ; Porcelli, Anna Maria ; Cricca, Monica ; Gasparre, Giuseppe</creator><creatorcontrib>Vidone, Michele ; Alessandrini, Federica ; Marucci, Gianluca ; Farnedi, Anna ; de Biase, Dario ; Ricceri, Fulvio ; Calabrese, Claudia ; Kurelac, Ivana ; Porcelli, Anna Maria ; Cricca, Monica ; Gasparre, Giuseppe</creatorcontrib><description>Glioblastoma multiforme (GBM) is the most malignant brain tumor in adults, but its etiology still remains unknown. Recently, a role of viruses such as cytomegalovirus and JC virus in gliomagenesis has been suggested. Since human papillomavirus (HPV) is considered the most common oncogenic virus in humans, we evaluated its occurrence in GBM samples.
Fifty-two formalin-fixed paraffin-embedded primary glioblastoma specimens were retrospectively analyzed. The presence of HPV genome on tumor DNA was assessed by MY/GP nested PCR. Confirmation of HPV detection was obtained by chromogenic in situ hybridization (CISH) and immunohistochemistry (IHC) with an antibody directed against the L1 capsidic protein. Finally, univariate and multivariate proportional-hazards models were used to compare the risk of death among HPV-positive and HPV-negative patients.
Strikingly, viral DNA was detected after PCR in 12 cases (23%). HPV16 genome was present in 25% infected samples, whereas the remaining samples tested positive for HPV6. CISH confirmed positivity in all infected samples for which enough material was available. Moreover, IHC positivity suggested that production of viral proteins from HPV genome is an ongoing process in GBM cancer cells. Finally an association between HPV infection and a worse prognosis was found in patients upon age stratification with a univariate analysis (HR, 2.10; 95% CI, 1.00-4.44; log-rank P = .045).
HPV infection status may be considered an independent prognostic factor in GBM patients and suggests that prevention may be considered, should HPV be recognized as a causative agent in gliomagenesis.</description><identifier>ISSN: 1522-8517</identifier><identifier>EISSN: 1523-5866</identifier><identifier>DOI: 10.1093/neuonc/not140</identifier><identifier>PMID: 24285549</identifier><language>eng</language><publisher>England: Oxford University Press</publisher><subject>Adult ; Aged ; Brain Neoplasms - mortality ; Brain Neoplasms - pathology ; Brain Neoplasms - virology ; Capsid Proteins - metabolism ; Clinical Research ; DNA, Viral - genetics ; Female ; Follow-Up Studies ; Glioblastoma - mortality ; Glioblastoma - pathology ; Glioblastoma - virology ; Human papillomavirus 16 - genetics ; Human papillomavirus 16 - isolation & purification ; Human papillomavirus 6 - genetics ; Human papillomavirus 6 - isolation & purification ; Humans ; Immunoenzyme Techniques ; In Situ Hybridization ; Male ; Middle Aged ; Papillomavirus Infections - mortality ; Papillomavirus Infections - pathology ; Papillomavirus Infections - virology ; Paraffin Embedding ; Polymerase Chain Reaction ; Prognosis ; Retrospective Studies ; Survival Rate</subject><ispartof>Neuro-oncology (Charlottesville, Va.), 2014-01, Vol.16 (2), p.298-302</ispartof><rights>The Author(s) 2013. Published by Oxford University Press on behalf of the Society for Neuro-Oncology. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com. 2013</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c387t-e9835b5eb61b705e1b6dc2965144ba50e853b2af97a59b5d6b8d1481db3062cd3</citedby><cites>FETCH-LOGICAL-c387t-e9835b5eb61b705e1b6dc2965144ba50e853b2af97a59b5d6b8d1481db3062cd3</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/PMC3895373/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3895373/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,315,728,781,785,886,27929,27930,53796,53798</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24285549$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Vidone, Michele</creatorcontrib><creatorcontrib>Alessandrini, Federica</creatorcontrib><creatorcontrib>Marucci, Gianluca</creatorcontrib><creatorcontrib>Farnedi, Anna</creatorcontrib><creatorcontrib>de Biase, Dario</creatorcontrib><creatorcontrib>Ricceri, Fulvio</creatorcontrib><creatorcontrib>Calabrese, Claudia</creatorcontrib><creatorcontrib>Kurelac, Ivana</creatorcontrib><creatorcontrib>Porcelli, Anna Maria</creatorcontrib><creatorcontrib>Cricca, Monica</creatorcontrib><creatorcontrib>Gasparre, Giuseppe</creatorcontrib><title>Evidence of association of human papillomavirus with prognosis worsening in glioblastoma multiforme</title><title>Neuro-oncology (Charlottesville, Va.)</title><addtitle>Neuro Oncol</addtitle><description>Glioblastoma multiforme (GBM) is the most malignant brain tumor in adults, but its etiology still remains unknown. Recently, a role of viruses such as cytomegalovirus and JC virus in gliomagenesis has been suggested. Since human papillomavirus (HPV) is considered the most common oncogenic virus in humans, we evaluated its occurrence in GBM samples.
Fifty-two formalin-fixed paraffin-embedded primary glioblastoma specimens were retrospectively analyzed. The presence of HPV genome on tumor DNA was assessed by MY/GP nested PCR. Confirmation of HPV detection was obtained by chromogenic in situ hybridization (CISH) and immunohistochemistry (IHC) with an antibody directed against the L1 capsidic protein. Finally, univariate and multivariate proportional-hazards models were used to compare the risk of death among HPV-positive and HPV-negative patients.
Strikingly, viral DNA was detected after PCR in 12 cases (23%). HPV16 genome was present in 25% infected samples, whereas the remaining samples tested positive for HPV6. CISH confirmed positivity in all infected samples for which enough material was available. Moreover, IHC positivity suggested that production of viral proteins from HPV genome is an ongoing process in GBM cancer cells. Finally an association between HPV infection and a worse prognosis was found in patients upon age stratification with a univariate analysis (HR, 2.10; 95% CI, 1.00-4.44; log-rank P = .045).
HPV infection status may be considered an independent prognostic factor in GBM patients and suggests that prevention may be considered, should HPV be recognized as a causative agent in gliomagenesis.</description><subject>Adult</subject><subject>Aged</subject><subject>Brain Neoplasms - mortality</subject><subject>Brain Neoplasms - pathology</subject><subject>Brain Neoplasms - virology</subject><subject>Capsid Proteins - metabolism</subject><subject>Clinical Research</subject><subject>DNA, Viral - genetics</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Glioblastoma - mortality</subject><subject>Glioblastoma - pathology</subject><subject>Glioblastoma - virology</subject><subject>Human papillomavirus 16 - genetics</subject><subject>Human papillomavirus 16 - isolation & purification</subject><subject>Human papillomavirus 6 - genetics</subject><subject>Human papillomavirus 6 - isolation & purification</subject><subject>Humans</subject><subject>Immunoenzyme Techniques</subject><subject>In Situ Hybridization</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Papillomavirus Infections - mortality</subject><subject>Papillomavirus Infections - pathology</subject><subject>Papillomavirus Infections - virology</subject><subject>Paraffin Embedding</subject><subject>Polymerase Chain Reaction</subject><subject>Prognosis</subject><subject>Retrospective Studies</subject><subject>Survival Rate</subject><issn>1522-8517</issn><issn>1523-5866</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkU1LxDAQhoMo7rp69Co9eqmbNE2bXARZ1g9Y8KLnkKRpN5ImNWlX_Pd27Sp6mhnm4Z2BB4BLBG8QZHjp9OCdWjrfoxwegTkiGU4JLYrj7z5LKUHlDJzF-AZhhkiBTsEsyzNKSM7mQK13ptJO6cTXiYjRKyN6491-3A6tcEknOmOtb8XOhCEmH6bfJl3wjfPRjKMPUTvjmsS4pLHGSytiP9JJO9je1D60-hyc1MJGfXGoC_B6v35ZPaab54en1d0mVZiWfaoZxUQSLQskS0g0kkWlMlYQlOdSEKgpwTITNSsFYZJUhaQVyimqJIZFpiq8ALdTbjfIVldKuz4Iy7tgWhE-uReG_984s-WN33FMGcElHgOuDwHBvw869rw1UWlrhdN-iBzlDDKIEGMjmk6oCj7GoOvfMwjyvRg-ieGTmJG_-vvbL_1jAn8Be26PyQ</recordid><startdate>201401</startdate><enddate>201401</enddate><creator>Vidone, Michele</creator><creator>Alessandrini, Federica</creator><creator>Marucci, Gianluca</creator><creator>Farnedi, Anna</creator><creator>de Biase, Dario</creator><creator>Ricceri, Fulvio</creator><creator>Calabrese, Claudia</creator><creator>Kurelac, Ivana</creator><creator>Porcelli, Anna Maria</creator><creator>Cricca, Monica</creator><creator>Gasparre, Giuseppe</creator><general>Oxford University Press</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>201401</creationdate><title>Evidence of association of human papillomavirus with prognosis worsening in glioblastoma multiforme</title><author>Vidone, Michele ; Alessandrini, Federica ; Marucci, Gianluca ; Farnedi, Anna ; de Biase, Dario ; Ricceri, Fulvio ; Calabrese, Claudia ; Kurelac, Ivana ; Porcelli, Anna Maria ; Cricca, Monica ; Gasparre, Giuseppe</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c387t-e9835b5eb61b705e1b6dc2965144ba50e853b2af97a59b5d6b8d1481db3062cd3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Brain Neoplasms - mortality</topic><topic>Brain Neoplasms - pathology</topic><topic>Brain Neoplasms - virology</topic><topic>Capsid Proteins - metabolism</topic><topic>Clinical Research</topic><topic>DNA, Viral - genetics</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Glioblastoma - mortality</topic><topic>Glioblastoma - pathology</topic><topic>Glioblastoma - virology</topic><topic>Human papillomavirus 16 - genetics</topic><topic>Human papillomavirus 16 - isolation & purification</topic><topic>Human papillomavirus 6 - genetics</topic><topic>Human papillomavirus 6 - isolation & purification</topic><topic>Humans</topic><topic>Immunoenzyme Techniques</topic><topic>In Situ Hybridization</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Papillomavirus Infections - mortality</topic><topic>Papillomavirus Infections - pathology</topic><topic>Papillomavirus Infections - virology</topic><topic>Paraffin Embedding</topic><topic>Polymerase Chain Reaction</topic><topic>Prognosis</topic><topic>Retrospective Studies</topic><topic>Survival Rate</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Vidone, Michele</creatorcontrib><creatorcontrib>Alessandrini, Federica</creatorcontrib><creatorcontrib>Marucci, Gianluca</creatorcontrib><creatorcontrib>Farnedi, Anna</creatorcontrib><creatorcontrib>de Biase, Dario</creatorcontrib><creatorcontrib>Ricceri, Fulvio</creatorcontrib><creatorcontrib>Calabrese, Claudia</creatorcontrib><creatorcontrib>Kurelac, Ivana</creatorcontrib><creatorcontrib>Porcelli, Anna Maria</creatorcontrib><creatorcontrib>Cricca, Monica</creatorcontrib><creatorcontrib>Gasparre, Giuseppe</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Neuro-oncology (Charlottesville, Va.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Vidone, Michele</au><au>Alessandrini, Federica</au><au>Marucci, Gianluca</au><au>Farnedi, Anna</au><au>de Biase, Dario</au><au>Ricceri, Fulvio</au><au>Calabrese, Claudia</au><au>Kurelac, Ivana</au><au>Porcelli, Anna Maria</au><au>Cricca, Monica</au><au>Gasparre, Giuseppe</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Evidence of association of human papillomavirus with prognosis worsening in glioblastoma multiforme</atitle><jtitle>Neuro-oncology (Charlottesville, Va.)</jtitle><addtitle>Neuro Oncol</addtitle><date>2014-01</date><risdate>2014</risdate><volume>16</volume><issue>2</issue><spage>298</spage><epage>302</epage><pages>298-302</pages><issn>1522-8517</issn><eissn>1523-5866</eissn><abstract>Glioblastoma multiforme (GBM) is the most malignant brain tumor in adults, but its etiology still remains unknown. Recently, a role of viruses such as cytomegalovirus and JC virus in gliomagenesis has been suggested. Since human papillomavirus (HPV) is considered the most common oncogenic virus in humans, we evaluated its occurrence in GBM samples.
Fifty-two formalin-fixed paraffin-embedded primary glioblastoma specimens were retrospectively analyzed. The presence of HPV genome on tumor DNA was assessed by MY/GP nested PCR. Confirmation of HPV detection was obtained by chromogenic in situ hybridization (CISH) and immunohistochemistry (IHC) with an antibody directed against the L1 capsidic protein. Finally, univariate and multivariate proportional-hazards models were used to compare the risk of death among HPV-positive and HPV-negative patients.
Strikingly, viral DNA was detected after PCR in 12 cases (23%). HPV16 genome was present in 25% infected samples, whereas the remaining samples tested positive for HPV6. CISH confirmed positivity in all infected samples for which enough material was available. Moreover, IHC positivity suggested that production of viral proteins from HPV genome is an ongoing process in GBM cancer cells. Finally an association between HPV infection and a worse prognosis was found in patients upon age stratification with a univariate analysis (HR, 2.10; 95% CI, 1.00-4.44; log-rank P = .045).
HPV infection status may be considered an independent prognostic factor in GBM patients and suggests that prevention may be considered, should HPV be recognized as a causative agent in gliomagenesis.</abstract><cop>England</cop><pub>Oxford University Press</pub><pmid>24285549</pmid><doi>10.1093/neuonc/not140</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1522-8517 |
ispartof | Neuro-oncology (Charlottesville, Va.), 2014-01, Vol.16 (2), p.298-302 |
issn | 1522-8517 1523-5866 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3895373 |
source | MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Oxford University Press Journals All Titles (1996-Current); PubMed Central |
subjects | Adult Aged Brain Neoplasms - mortality Brain Neoplasms - pathology Brain Neoplasms - virology Capsid Proteins - metabolism Clinical Research DNA, Viral - genetics Female Follow-Up Studies Glioblastoma - mortality Glioblastoma - pathology Glioblastoma - virology Human papillomavirus 16 - genetics Human papillomavirus 16 - isolation & purification Human papillomavirus 6 - genetics Human papillomavirus 6 - isolation & purification Humans Immunoenzyme Techniques In Situ Hybridization Male Middle Aged Papillomavirus Infections - mortality Papillomavirus Infections - pathology Papillomavirus Infections - virology Paraffin Embedding Polymerase Chain Reaction Prognosis Retrospective Studies Survival Rate |
title | Evidence of association of human papillomavirus with prognosis worsening in glioblastoma multiforme |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-12T18%3A11%3A29IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Evidence%20of%20association%20of%20human%20papillomavirus%20with%20prognosis%20worsening%20in%20glioblastoma%20multiforme&rft.jtitle=Neuro-oncology%20(Charlottesville,%20Va.)&rft.au=Vidone,%20Michele&rft.date=2014-01&rft.volume=16&rft.issue=2&rft.spage=298&rft.epage=302&rft.pages=298-302&rft.issn=1522-8517&rft.eissn=1523-5866&rft_id=info:doi/10.1093/neuonc/not140&rft_dat=%3Cproquest_pubme%3E1490901199%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1490901199&rft_id=info:pmid/24285549&rfr_iscdi=true |