Loading…
Elucidating cellular response to treatment with viral immunotherapies in pediatric high-grade glioma and medulloblastoma
HSV G207, a double-stranded, DNA virus, and the polio:rhinovirus chimera, PVSRIPO, a single positive-strand RNA virus, are viral immunotherapies being used to treat pediatric malignant brain tumors in clinical trials. The purpose of this work is to elucidate general response patterns and putative bi...
Saved in:
Published in: | Translational oncology 2024-02, Vol.40, p.101875, Article 101875 |
---|---|
Main Authors: | , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c405t-65347ac62a0dd3fa9220fa0380b79ea21aa216d7d78b3c96379bb4babf73eb103 |
---|---|
cites | cdi_FETCH-LOGICAL-c405t-65347ac62a0dd3fa9220fa0380b79ea21aa216d7d78b3c96379bb4babf73eb103 |
container_end_page | |
container_issue | |
container_start_page | 101875 |
container_title | Translational oncology |
container_volume | 40 |
creator | Thompson, Eric M Kang, Kyung-Don Stevenson, Kevin Zhang, Hengshan Gromeier, Matthias Ashley, David Brown, Michael Friedman, Gregory K |
description | HSV G207, a double-stranded, DNA virus, and the polio:rhinovirus chimera, PVSRIPO, a single positive-strand RNA virus, are viral immunotherapies being used to treat pediatric malignant brain tumors in clinical trials. The purpose of this work is to elucidate general response patterns and putative biomarkers of response. Multiple pediatric high-grade glioma and medulloblastoma cell lines were treated with various multiplicities of infection of G207 or PVSRIPO. There was a significant inverse correlation between expression of one HSV cellular receptor, CD111, and the lethal dose of 50% of cells (LD50) of cells treated with G207 (r = -0.985, P |
doi_str_mv | 10.1016/j.tranon.2024.101875 |
format | article |
fullrecord | <record><control><sourceid>proquest_doaj_</sourceid><recordid>TN_cdi_doaj_primary_oai_doaj_org_article_a1861e1580df46258533f5041fbd02cc</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><doaj_id>oai_doaj_org_article_a1861e1580df46258533f5041fbd02cc</doaj_id><sourcerecordid>2915572195</sourcerecordid><originalsourceid>FETCH-LOGICAL-c405t-65347ac62a0dd3fa9220fa0380b79ea21aa216d7d78b3c96379bb4babf73eb103</originalsourceid><addsrcrecordid>eNpVUstu1TAUjBCIlsIfIOQlm1z8iPNYIVSVtlIlNrC2jh9JfOXYwXYK_D2-pFTtwrI1PmfOeDxV9Z7gA8Gk_XQ85Ag--APFtDlBfcdfVOdkYG3NKWMvn5zPqjcpHTFuyUDp6-qM9aRnPabn1e8rtymrIVs_IWWc2xxEFE1ag08G5YByNJAX4zP6ZfOM7m0Eh-yybD7k2URYrUnIerQabSFHq9Bsp7meImiDJmfDAgi8RovRm3NBOki5YG-rVyO4ZN497BfVj69X3y9v6rtv17eXX-5q1WCe65azpgPVUsBasxGKfjwCLuJlNxigBMpqdae7XjI1tKwbpGwkyLFjRhLMLqrbnVcHOIo12gXiHxHAin9AiJOAmK1yRgDpW2II77Eem5bynjM2ctyQUWpMlSpcn3eudZPlOaqYUsx4Rvr8xttZTOFeENzjgZCuMHx8YIjh52ZSFotNJ9vBm7AlQQfCeUfJwEtps5eqGFKKZnycQ7A4JUAcxZ4AcUqA2BNQ2j481fjY9P_L2V_JXLJZ</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2915572195</pqid></control><display><type>article</type><title>Elucidating cellular response to treatment with viral immunotherapies in pediatric high-grade glioma and medulloblastoma</title><source>ScienceDirect®</source><source>PubMed Central</source><creator>Thompson, Eric M ; Kang, Kyung-Don ; Stevenson, Kevin ; Zhang, Hengshan ; Gromeier, Matthias ; Ashley, David ; Brown, Michael ; Friedman, Gregory K</creator><creatorcontrib>Thompson, Eric M ; Kang, Kyung-Don ; Stevenson, Kevin ; Zhang, Hengshan ; Gromeier, Matthias ; Ashley, David ; Brown, Michael ; Friedman, Gregory K</creatorcontrib><description>HSV G207, a double-stranded, DNA virus, and the polio:rhinovirus chimera, PVSRIPO, a single positive-strand RNA virus, are viral immunotherapies being used to treat pediatric malignant brain tumors in clinical trials. The purpose of this work is to elucidate general response patterns and putative biomarkers of response. Multiple pediatric high-grade glioma and medulloblastoma cell lines were treated with various multiplicities of infection of G207 or PVSRIPO. There was a significant inverse correlation between expression of one HSV cellular receptor, CD111, and the lethal dose of 50% of cells (LD50) of cells treated with G207 (r = -0.985, P<0.001) but no correlation between PVSRIPO cellular receptor expression (CD155) and LD50. RNA sequencing of control cells and cells treated for 8 and 24 h revealed that there were few shared differentially expressed (DE) genes between cells treated with PVSRIPO and G207: GCLM, LANCL2, and RBM3 were enriched whilst ADAMTS1 and VEGFA were depleted. Likewise, there were few shared DE genes enriched between medulloblastoma and high-grade glioma cell lines treated with G207: GPSM2, CHECK2, SEPTIN2, EIF4G2, GCLM, GDAP1, LANCL2, and PWP1. Treatment with G207 and PVSRIPO appear to cause disparate gene enrichment and depletion suggesting disparate molecular mechanisms in malignant pediatric brain tumors.</description><identifier>ISSN: 1936-5233</identifier><identifier>EISSN: 1936-5233</identifier><identifier>DOI: 10.1016/j.tranon.2024.101875</identifier><identifier>PMID: 38183802</identifier><language>eng</language><publisher>United States: Neoplasia Press</publisher><subject>G207 ; Medulloblastoma ; Oncolytic virus ; Original Research ; Pediatric high-grade glioma ; PVSRIPO ; Viral immunotherapy</subject><ispartof>Translational oncology, 2024-02, Vol.40, p.101875, Article 101875</ispartof><rights>Copyright © 2024. Published by Elsevier Inc.</rights><rights>2024 The Authors. Published by Elsevier Inc. 2024</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c405t-65347ac62a0dd3fa9220fa0380b79ea21aa216d7d78b3c96379bb4babf73eb103</citedby><cites>FETCH-LOGICAL-c405t-65347ac62a0dd3fa9220fa0380b79ea21aa216d7d78b3c96379bb4babf73eb103</cites><orcidid>0000-0002-6260-3902 ; 0000-0002-3957-1164 ; 0000-0003-2796-9914 ; 0000-0002-4754-5900</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10809117/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10809117/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38183802$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Thompson, Eric M</creatorcontrib><creatorcontrib>Kang, Kyung-Don</creatorcontrib><creatorcontrib>Stevenson, Kevin</creatorcontrib><creatorcontrib>Zhang, Hengshan</creatorcontrib><creatorcontrib>Gromeier, Matthias</creatorcontrib><creatorcontrib>Ashley, David</creatorcontrib><creatorcontrib>Brown, Michael</creatorcontrib><creatorcontrib>Friedman, Gregory K</creatorcontrib><title>Elucidating cellular response to treatment with viral immunotherapies in pediatric high-grade glioma and medulloblastoma</title><title>Translational oncology</title><addtitle>Transl Oncol</addtitle><description>HSV G207, a double-stranded, DNA virus, and the polio:rhinovirus chimera, PVSRIPO, a single positive-strand RNA virus, are viral immunotherapies being used to treat pediatric malignant brain tumors in clinical trials. The purpose of this work is to elucidate general response patterns and putative biomarkers of response. Multiple pediatric high-grade glioma and medulloblastoma cell lines were treated with various multiplicities of infection of G207 or PVSRIPO. There was a significant inverse correlation between expression of one HSV cellular receptor, CD111, and the lethal dose of 50% of cells (LD50) of cells treated with G207 (r = -0.985, P<0.001) but no correlation between PVSRIPO cellular receptor expression (CD155) and LD50. RNA sequencing of control cells and cells treated for 8 and 24 h revealed that there were few shared differentially expressed (DE) genes between cells treated with PVSRIPO and G207: GCLM, LANCL2, and RBM3 were enriched whilst ADAMTS1 and VEGFA were depleted. Likewise, there were few shared DE genes enriched between medulloblastoma and high-grade glioma cell lines treated with G207: GPSM2, CHECK2, SEPTIN2, EIF4G2, GCLM, GDAP1, LANCL2, and PWP1. Treatment with G207 and PVSRIPO appear to cause disparate gene enrichment and depletion suggesting disparate molecular mechanisms in malignant pediatric brain tumors.</description><subject>G207</subject><subject>Medulloblastoma</subject><subject>Oncolytic virus</subject><subject>Original Research</subject><subject>Pediatric high-grade glioma</subject><subject>PVSRIPO</subject><subject>Viral immunotherapy</subject><issn>1936-5233</issn><issn>1936-5233</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNpVUstu1TAUjBCIlsIfIOQlm1z8iPNYIVSVtlIlNrC2jh9JfOXYwXYK_D2-pFTtwrI1PmfOeDxV9Z7gA8Gk_XQ85Ag--APFtDlBfcdfVOdkYG3NKWMvn5zPqjcpHTFuyUDp6-qM9aRnPabn1e8rtymrIVs_IWWc2xxEFE1ag08G5YByNJAX4zP6ZfOM7m0Eh-yybD7k2URYrUnIerQabSFHq9Bsp7meImiDJmfDAgi8RovRm3NBOki5YG-rVyO4ZN497BfVj69X3y9v6rtv17eXX-5q1WCe65azpgPVUsBasxGKfjwCLuJlNxigBMpqdae7XjI1tKwbpGwkyLFjRhLMLqrbnVcHOIo12gXiHxHAin9AiJOAmK1yRgDpW2II77Eem5bynjM2ctyQUWpMlSpcn3eudZPlOaqYUsx4Rvr8xttZTOFeENzjgZCuMHx8YIjh52ZSFotNJ9vBm7AlQQfCeUfJwEtps5eqGFKKZnycQ7A4JUAcxZ4AcUqA2BNQ2j481fjY9P_L2V_JXLJZ</recordid><startdate>20240201</startdate><enddate>20240201</enddate><creator>Thompson, Eric M</creator><creator>Kang, Kyung-Don</creator><creator>Stevenson, Kevin</creator><creator>Zhang, Hengshan</creator><creator>Gromeier, Matthias</creator><creator>Ashley, David</creator><creator>Brown, Michael</creator><creator>Friedman, Gregory K</creator><general>Neoplasia Press</general><general>Elsevier</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-6260-3902</orcidid><orcidid>https://orcid.org/0000-0002-3957-1164</orcidid><orcidid>https://orcid.org/0000-0003-2796-9914</orcidid><orcidid>https://orcid.org/0000-0002-4754-5900</orcidid></search><sort><creationdate>20240201</creationdate><title>Elucidating cellular response to treatment with viral immunotherapies in pediatric high-grade glioma and medulloblastoma</title><author>Thompson, Eric M ; Kang, Kyung-Don ; Stevenson, Kevin ; Zhang, Hengshan ; Gromeier, Matthias ; Ashley, David ; Brown, Michael ; Friedman, Gregory K</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c405t-65347ac62a0dd3fa9220fa0380b79ea21aa216d7d78b3c96379bb4babf73eb103</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>G207</topic><topic>Medulloblastoma</topic><topic>Oncolytic virus</topic><topic>Original Research</topic><topic>Pediatric high-grade glioma</topic><topic>PVSRIPO</topic><topic>Viral immunotherapy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Thompson, Eric M</creatorcontrib><creatorcontrib>Kang, Kyung-Don</creatorcontrib><creatorcontrib>Stevenson, Kevin</creatorcontrib><creatorcontrib>Zhang, Hengshan</creatorcontrib><creatorcontrib>Gromeier, Matthias</creatorcontrib><creatorcontrib>Ashley, David</creatorcontrib><creatorcontrib>Brown, Michael</creatorcontrib><creatorcontrib>Friedman, Gregory K</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Translational oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Thompson, Eric M</au><au>Kang, Kyung-Don</au><au>Stevenson, Kevin</au><au>Zhang, Hengshan</au><au>Gromeier, Matthias</au><au>Ashley, David</au><au>Brown, Michael</au><au>Friedman, Gregory K</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Elucidating cellular response to treatment with viral immunotherapies in pediatric high-grade glioma and medulloblastoma</atitle><jtitle>Translational oncology</jtitle><addtitle>Transl Oncol</addtitle><date>2024-02-01</date><risdate>2024</risdate><volume>40</volume><spage>101875</spage><pages>101875-</pages><artnum>101875</artnum><issn>1936-5233</issn><eissn>1936-5233</eissn><abstract>HSV G207, a double-stranded, DNA virus, and the polio:rhinovirus chimera, PVSRIPO, a single positive-strand RNA virus, are viral immunotherapies being used to treat pediatric malignant brain tumors in clinical trials. The purpose of this work is to elucidate general response patterns and putative biomarkers of response. Multiple pediatric high-grade glioma and medulloblastoma cell lines were treated with various multiplicities of infection of G207 or PVSRIPO. There was a significant inverse correlation between expression of one HSV cellular receptor, CD111, and the lethal dose of 50% of cells (LD50) of cells treated with G207 (r = -0.985, P<0.001) but no correlation between PVSRIPO cellular receptor expression (CD155) and LD50. RNA sequencing of control cells and cells treated for 8 and 24 h revealed that there were few shared differentially expressed (DE) genes between cells treated with PVSRIPO and G207: GCLM, LANCL2, and RBM3 were enriched whilst ADAMTS1 and VEGFA were depleted. Likewise, there were few shared DE genes enriched between medulloblastoma and high-grade glioma cell lines treated with G207: GPSM2, CHECK2, SEPTIN2, EIF4G2, GCLM, GDAP1, LANCL2, and PWP1. Treatment with G207 and PVSRIPO appear to cause disparate gene enrichment and depletion suggesting disparate molecular mechanisms in malignant pediatric brain tumors.</abstract><cop>United States</cop><pub>Neoplasia Press</pub><pmid>38183802</pmid><doi>10.1016/j.tranon.2024.101875</doi><orcidid>https://orcid.org/0000-0002-6260-3902</orcidid><orcidid>https://orcid.org/0000-0002-3957-1164</orcidid><orcidid>https://orcid.org/0000-0003-2796-9914</orcidid><orcidid>https://orcid.org/0000-0002-4754-5900</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1936-5233 |
ispartof | Translational oncology, 2024-02, Vol.40, p.101875, Article 101875 |
issn | 1936-5233 1936-5233 |
language | eng |
recordid | cdi_doaj_primary_oai_doaj_org_article_a1861e1580df46258533f5041fbd02cc |
source | ScienceDirect®; PubMed Central |
subjects | G207 Medulloblastoma Oncolytic virus Original Research Pediatric high-grade glioma PVSRIPO Viral immunotherapy |
title | Elucidating cellular response to treatment with viral immunotherapies in pediatric high-grade glioma and medulloblastoma |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-27T19%3A03%3A15IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_doaj_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Elucidating%20cellular%20response%20to%20treatment%20with%20viral%20immunotherapies%20in%20pediatric%20high-grade%20glioma%20and%20medulloblastoma&rft.jtitle=Translational%20oncology&rft.au=Thompson,%20Eric%20M&rft.date=2024-02-01&rft.volume=40&rft.spage=101875&rft.pages=101875-&rft.artnum=101875&rft.issn=1936-5233&rft.eissn=1936-5233&rft_id=info:doi/10.1016/j.tranon.2024.101875&rft_dat=%3Cproquest_doaj_%3E2915572195%3C/proquest_doaj_%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c405t-65347ac62a0dd3fa9220fa0380b79ea21aa216d7d78b3c96379bb4babf73eb103%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2915572195&rft_id=info:pmid/38183802&rfr_iscdi=true |