DIPG-70. NQO1 AS A RESISTANCE DRIVER AND THERAPEUTIC TARGET IN DMG

p53 pathway reactivation through pharmacologic inhibition of negative regulators was identified as a promising therapeutic strategy for TP53 wild-type (WT) high-grade gliomas, including Diffuse Midline Gliomas (DMGs). Despite widespread theoretical promise, the therapeutic efficacy of MDM2 inhibitor...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Neuro-oncology (Charlottesville, Va.) Va.), 2024-06, Vol.26 (Supplement_4), p.0-0
Hauptverfasser: Lupien, Leslie E, Morin, Eric, Zhang, Daren F, Novikov, Dana R, Chacon, Madison S, Khuu, Nicholas, Keshishian, Hasmik, Seidel, Olivia, Carr, Steven A, Goodale, Amy, Persky, Nicole S, Root, David E, Cusick, Margaret, Ligon, Keith L, Beroukhim, Rameen, Phoenix, Timothy M, Rendo, Veronica, Bandopadhayay, Pratiti
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 0
container_issue Supplement_4
container_start_page 0
container_title Neuro-oncology (Charlottesville, Va.)
container_volume 26
creator Lupien, Leslie E
Morin, Eric
Zhang, Daren F
Novikov, Dana R
Chacon, Madison S
Khuu, Nicholas
Keshishian, Hasmik
Seidel, Olivia
Carr, Steven A
Goodale, Amy
Persky, Nicole S
Root, David E
Cusick, Margaret
Ligon, Keith L
Beroukhim, Rameen
Phoenix, Timothy M
Rendo, Veronica
Bandopadhayay, Pratiti
description p53 pathway reactivation through pharmacologic inhibition of negative regulators was identified as a promising therapeutic strategy for TP53 wild-type (WT) high-grade gliomas, including Diffuse Midline Gliomas (DMGs). Despite widespread theoretical promise, the therapeutic efficacy of MDM2 inhibitors and PPM1D inhibitors as single agents have each been limited by issues, including sub-lethal effects on cancer cells and innate or emerging resistance leading to tumor progression. We carried out a genome-scale CRISPR activating (CRISPRa) screen to identify genes that, when overexpressed, confer resistance to p53 reactivation therapies. NAD(P)H quinone dehydrogenase 1 (NQO1) emerged as a top hit and was confirmed through secondary CRISPRa screens and low-throughput validations as driving a resistance phenotype in TP53 WT DMGs. Our subsequent work has aimed to elucidate the mechanisms through which NQO1 mediates the effects of p53 reactivation therapies, and assess the feasibility and impact of exploiting NQO1 in combination therapies towards a cure.
doi_str_mv 10.1093/neuonc/noae064.123
format Article
fullrecord <record><control><sourceid>pubmedcentral_cross</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_11182908</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>pubmedcentral_primary_oai_pubmedcentral_nih_gov_11182908</sourcerecordid><originalsourceid>FETCH-LOGICAL-c1433-f8d9a062f0d8b2f0cf32758f603da6c80c33bb078b55aa53e282f03d65823ad3</originalsourceid><addsrcrecordid>eNpVkMtOwzAQRS0EEqXwA6z8A2n9qB13hUxi0kglLYlhazmOA0VtUiUUib8n0AqJzdyRZu5ZHABuMZpgNKfTxh_axk2b1nrEZxNM6BkYYUZowATn5787CQTD4SW46vt3hAhmHI_AfZyukyBEE5g9rTCUBZQwV0VaaJlFCsZ5-qJyKLMY6oXK5Vo96zSCWuaJ0jDNYPyYXIOL2m57f3PKMdAPSkeLYLlK0kguA4dnlAa1qOYWcVKjSpTDdDUlIRM1R7Sy3AnkKC1LFIqSMWsZ9UQMX7TiTBBqKzoGd0fs_lDufOV889HZrdl3m53tvkxrN-b_pdm8mdf202CMBZkjMRDIkeC6tu87X_-VMTI_Gs1RozlpNING-g3KGmMb</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>DIPG-70. NQO1 AS A RESISTANCE DRIVER AND THERAPEUTIC TARGET IN DMG</title><source>Oxford University Press Journals All Titles (1996-Current)</source><creator>Lupien, Leslie E ; Morin, Eric ; Zhang, Daren F ; Novikov, Dana R ; Chacon, Madison S ; Khuu, Nicholas ; Keshishian, Hasmik ; Seidel, Olivia ; Carr, Steven A ; Goodale, Amy ; Persky, Nicole S ; Root, David E ; Cusick, Margaret ; Ligon, Keith L ; Beroukhim, Rameen ; Phoenix, Timothy M ; Rendo, Veronica ; Bandopadhayay, Pratiti</creator><creatorcontrib>Lupien, Leslie E ; Morin, Eric ; Zhang, Daren F ; Novikov, Dana R ; Chacon, Madison S ; Khuu, Nicholas ; Keshishian, Hasmik ; Seidel, Olivia ; Carr, Steven A ; Goodale, Amy ; Persky, Nicole S ; Root, David E ; Cusick, Margaret ; Ligon, Keith L ; Beroukhim, Rameen ; Phoenix, Timothy M ; Rendo, Veronica ; Bandopadhayay, Pratiti</creatorcontrib><description>p53 pathway reactivation through pharmacologic inhibition of negative regulators was identified as a promising therapeutic strategy for TP53 wild-type (WT) high-grade gliomas, including Diffuse Midline Gliomas (DMGs). Despite widespread theoretical promise, the therapeutic efficacy of MDM2 inhibitors and PPM1D inhibitors as single agents have each been limited by issues, including sub-lethal effects on cancer cells and innate or emerging resistance leading to tumor progression. We carried out a genome-scale CRISPR activating (CRISPRa) screen to identify genes that, when overexpressed, confer resistance to p53 reactivation therapies. NAD(P)H quinone dehydrogenase 1 (NQO1) emerged as a top hit and was confirmed through secondary CRISPRa screens and low-throughput validations as driving a resistance phenotype in TP53 WT DMGs. Our subsequent work has aimed to elucidate the mechanisms through which NQO1 mediates the effects of p53 reactivation therapies, and assess the feasibility and impact of exploiting NQO1 in combination therapies towards a cure.</description><identifier>ISSN: 1522-8517</identifier><identifier>EISSN: 1523-5866</identifier><identifier>DOI: 10.1093/neuonc/noae064.123</identifier><language>eng</language><publisher>US: Oxford University Press</publisher><subject>Final category: Diffuse Midline Glioma, Diffuse Intrinsic Pontine Glioma</subject><ispartof>Neuro-oncology (Charlottesville, Va.), 2024-06, Vol.26 (Supplement_4), p.0-0</ispartof><rights>The Author(s) 2024. Published by Oxford University Press on behalf of the Society for Neuro-Oncology. 2024</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,27901,27902</link.rule.ids></links><search><creatorcontrib>Lupien, Leslie E</creatorcontrib><creatorcontrib>Morin, Eric</creatorcontrib><creatorcontrib>Zhang, Daren F</creatorcontrib><creatorcontrib>Novikov, Dana R</creatorcontrib><creatorcontrib>Chacon, Madison S</creatorcontrib><creatorcontrib>Khuu, Nicholas</creatorcontrib><creatorcontrib>Keshishian, Hasmik</creatorcontrib><creatorcontrib>Seidel, Olivia</creatorcontrib><creatorcontrib>Carr, Steven A</creatorcontrib><creatorcontrib>Goodale, Amy</creatorcontrib><creatorcontrib>Persky, Nicole S</creatorcontrib><creatorcontrib>Root, David E</creatorcontrib><creatorcontrib>Cusick, Margaret</creatorcontrib><creatorcontrib>Ligon, Keith L</creatorcontrib><creatorcontrib>Beroukhim, Rameen</creatorcontrib><creatorcontrib>Phoenix, Timothy M</creatorcontrib><creatorcontrib>Rendo, Veronica</creatorcontrib><creatorcontrib>Bandopadhayay, Pratiti</creatorcontrib><title>DIPG-70. NQO1 AS A RESISTANCE DRIVER AND THERAPEUTIC TARGET IN DMG</title><title>Neuro-oncology (Charlottesville, Va.)</title><description>p53 pathway reactivation through pharmacologic inhibition of negative regulators was identified as a promising therapeutic strategy for TP53 wild-type (WT) high-grade gliomas, including Diffuse Midline Gliomas (DMGs). Despite widespread theoretical promise, the therapeutic efficacy of MDM2 inhibitors and PPM1D inhibitors as single agents have each been limited by issues, including sub-lethal effects on cancer cells and innate or emerging resistance leading to tumor progression. We carried out a genome-scale CRISPR activating (CRISPRa) screen to identify genes that, when overexpressed, confer resistance to p53 reactivation therapies. NAD(P)H quinone dehydrogenase 1 (NQO1) emerged as a top hit and was confirmed through secondary CRISPRa screens and low-throughput validations as driving a resistance phenotype in TP53 WT DMGs. Our subsequent work has aimed to elucidate the mechanisms through which NQO1 mediates the effects of p53 reactivation therapies, and assess the feasibility and impact of exploiting NQO1 in combination therapies towards a cure.</description><subject>Final category: Diffuse Midline Glioma, Diffuse Intrinsic Pontine Glioma</subject><issn>1522-8517</issn><issn>1523-5866</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNpVkMtOwzAQRS0EEqXwA6z8A2n9qB13hUxi0kglLYlhazmOA0VtUiUUib8n0AqJzdyRZu5ZHABuMZpgNKfTxh_axk2b1nrEZxNM6BkYYUZowATn5787CQTD4SW46vt3hAhmHI_AfZyukyBEE5g9rTCUBZQwV0VaaJlFCsZ5-qJyKLMY6oXK5Vo96zSCWuaJ0jDNYPyYXIOL2m57f3PKMdAPSkeLYLlK0kguA4dnlAa1qOYWcVKjSpTDdDUlIRM1R7Sy3AnkKC1LFIqSMWsZ9UQMX7TiTBBqKzoGd0fs_lDufOV889HZrdl3m53tvkxrN-b_pdm8mdf202CMBZkjMRDIkeC6tu87X_-VMTI_Gs1RozlpNING-g3KGmMb</recordid><startdate>20240618</startdate><enddate>20240618</enddate><creator>Lupien, Leslie E</creator><creator>Morin, Eric</creator><creator>Zhang, Daren F</creator><creator>Novikov, Dana R</creator><creator>Chacon, Madison S</creator><creator>Khuu, Nicholas</creator><creator>Keshishian, Hasmik</creator><creator>Seidel, Olivia</creator><creator>Carr, Steven A</creator><creator>Goodale, Amy</creator><creator>Persky, Nicole S</creator><creator>Root, David E</creator><creator>Cusick, Margaret</creator><creator>Ligon, Keith L</creator><creator>Beroukhim, Rameen</creator><creator>Phoenix, Timothy M</creator><creator>Rendo, Veronica</creator><creator>Bandopadhayay, Pratiti</creator><general>Oxford University Press</general><scope>AAYXX</scope><scope>CITATION</scope><scope>5PM</scope></search><sort><creationdate>20240618</creationdate><title>DIPG-70. NQO1 AS A RESISTANCE DRIVER AND THERAPEUTIC TARGET IN DMG</title><author>Lupien, Leslie E ; Morin, Eric ; Zhang, Daren F ; Novikov, Dana R ; Chacon, Madison S ; Khuu, Nicholas ; Keshishian, Hasmik ; Seidel, Olivia ; Carr, Steven A ; Goodale, Amy ; Persky, Nicole S ; Root, David E ; Cusick, Margaret ; Ligon, Keith L ; Beroukhim, Rameen ; Phoenix, Timothy M ; Rendo, Veronica ; Bandopadhayay, Pratiti</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c1433-f8d9a062f0d8b2f0cf32758f603da6c80c33bb078b55aa53e282f03d65823ad3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Final category: Diffuse Midline Glioma, Diffuse Intrinsic Pontine Glioma</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lupien, Leslie E</creatorcontrib><creatorcontrib>Morin, Eric</creatorcontrib><creatorcontrib>Zhang, Daren F</creatorcontrib><creatorcontrib>Novikov, Dana R</creatorcontrib><creatorcontrib>Chacon, Madison S</creatorcontrib><creatorcontrib>Khuu, Nicholas</creatorcontrib><creatorcontrib>Keshishian, Hasmik</creatorcontrib><creatorcontrib>Seidel, Olivia</creatorcontrib><creatorcontrib>Carr, Steven A</creatorcontrib><creatorcontrib>Goodale, Amy</creatorcontrib><creatorcontrib>Persky, Nicole S</creatorcontrib><creatorcontrib>Root, David E</creatorcontrib><creatorcontrib>Cusick, Margaret</creatorcontrib><creatorcontrib>Ligon, Keith L</creatorcontrib><creatorcontrib>Beroukhim, Rameen</creatorcontrib><creatorcontrib>Phoenix, Timothy M</creatorcontrib><creatorcontrib>Rendo, Veronica</creatorcontrib><creatorcontrib>Bandopadhayay, Pratiti</creatorcontrib><collection>CrossRef</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>Lupien, Leslie E</au><au>Morin, Eric</au><au>Zhang, Daren F</au><au>Novikov, Dana R</au><au>Chacon, Madison S</au><au>Khuu, Nicholas</au><au>Keshishian, Hasmik</au><au>Seidel, Olivia</au><au>Carr, Steven A</au><au>Goodale, Amy</au><au>Persky, Nicole S</au><au>Root, David E</au><au>Cusick, Margaret</au><au>Ligon, Keith L</au><au>Beroukhim, Rameen</au><au>Phoenix, Timothy M</au><au>Rendo, Veronica</au><au>Bandopadhayay, Pratiti</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>DIPG-70. NQO1 AS A RESISTANCE DRIVER AND THERAPEUTIC TARGET IN DMG</atitle><jtitle>Neuro-oncology (Charlottesville, Va.)</jtitle><date>2024-06-18</date><risdate>2024</risdate><volume>26</volume><issue>Supplement_4</issue><spage>0</spage><epage>0</epage><pages>0-0</pages><issn>1522-8517</issn><eissn>1523-5866</eissn><abstract>p53 pathway reactivation through pharmacologic inhibition of negative regulators was identified as a promising therapeutic strategy for TP53 wild-type (WT) high-grade gliomas, including Diffuse Midline Gliomas (DMGs). Despite widespread theoretical promise, the therapeutic efficacy of MDM2 inhibitors and PPM1D inhibitors as single agents have each been limited by issues, including sub-lethal effects on cancer cells and innate or emerging resistance leading to tumor progression. We carried out a genome-scale CRISPR activating (CRISPRa) screen to identify genes that, when overexpressed, confer resistance to p53 reactivation therapies. NAD(P)H quinone dehydrogenase 1 (NQO1) emerged as a top hit and was confirmed through secondary CRISPRa screens and low-throughput validations as driving a resistance phenotype in TP53 WT DMGs. Our subsequent work has aimed to elucidate the mechanisms through which NQO1 mediates the effects of p53 reactivation therapies, and assess the feasibility and impact of exploiting NQO1 in combination therapies towards a cure.</abstract><cop>US</cop><pub>Oxford University Press</pub><doi>10.1093/neuonc/noae064.123</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1522-8517
ispartof Neuro-oncology (Charlottesville, Va.), 2024-06, Vol.26 (Supplement_4), p.0-0
issn 1522-8517
1523-5866
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_11182908
source Oxford University Press Journals All Titles (1996-Current)
subjects Final category: Diffuse Midline Glioma, Diffuse Intrinsic Pontine Glioma
title DIPG-70. NQO1 AS A RESISTANCE DRIVER AND THERAPEUTIC TARGET IN DMG
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-30T10%3A20%3A15IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-pubmedcentral_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=DIPG-70.%20NQO1%20AS%20A%20RESISTANCE%20DRIVER%20AND%20THERAPEUTIC%20TARGET%20IN%20DMG&rft.jtitle=Neuro-oncology%20(Charlottesville,%20Va.)&rft.au=Lupien,%20Leslie%20E&rft.date=2024-06-18&rft.volume=26&rft.issue=Supplement_4&rft.spage=0&rft.epage=0&rft.pages=0-0&rft.issn=1522-8517&rft.eissn=1523-5866&rft_id=info:doi/10.1093/neuonc/noae064.123&rft_dat=%3Cpubmedcentral_cross%3Epubmedcentral_primary_oai_pubmedcentral_nih_gov_11182908%3C/pubmedcentral_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true