Cargando…

DDRE-24. TARGETING PURINE METABOLISM TO OVERCOME GLIOBLASTOMA THERAPY RESISTANCE

Intratumoral genomic heterogeneity in glioblastoma (GBM) is a barrier to overcoming radiation (RT) resistance. To discover genotype-independent mediators of RT resistance, we correlated RT resistance with the concentration of approximately 700 metabolites across 23 GBM cell lines. Purine metabolites...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhou, Weihua, Yao, Yangyang, Scott, Andrew, Wilder-Romans, Kari, Dresser, Joseph, Werner, Christian, Sun, Hanshi, Pratt, Drew, Sajjakulnukit, Peter, Zaho, Shuang, Davis, Mary, Nelson, Barbara, Halbrook, Christopher, Zhang, Li, Gatto, Francesco, Srinivasan, Sudharsan, Jairath, Neil, Correa, Luis, Umemura, Yoshie, Walker, Angela, Kachman, Maureen, Qi, Nathan, Sarkaria, Jann, Xiong, Jianping, Morgan, Meredith, Rehemtulla, Alnawaz, Castro, Maria, Lowenstein, Pedro, Chandrasekaran, Sriram, Lawrence, Theodore, Lyssiotis, Costas, Wahl, Daniel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7992262/
http://dx.doi.org/10.1093/noajnl/vdab024.046
_version_ 1783669337515622400
author Zhou, Weihua
Yao, Yangyang
Scott, Andrew
Wilder-Romans, Kari
Dresser, Joseph
Werner, Christian
Sun, Hanshi
Pratt, Drew
Sajjakulnukit, Peter
Zaho, Shuang
Davis, Mary
Nelson, Barbara
Halbrook, Christopher
Zhang, Li
Gatto, Francesco
Srinivasan, Sudharsan
Jairath, Neil
Correa, Luis
Umemura, Yoshie
Walker, Angela
Kachman, Maureen
Qi, Nathan
Sarkaria, Jann
Xiong, Jianping
Morgan, Meredith
Rehemtulla, Alnawaz
Castro, Maria
Lowenstein, Pedro
Chandrasekaran, Sriram
Lawrence, Theodore
Lyssiotis, Costas
Wahl, Daniel
author_facet Zhou, Weihua
Yao, Yangyang
Scott, Andrew
Wilder-Romans, Kari
Dresser, Joseph
Werner, Christian
Sun, Hanshi
Pratt, Drew
Sajjakulnukit, Peter
Zaho, Shuang
Davis, Mary
Nelson, Barbara
Halbrook, Christopher
Zhang, Li
Gatto, Francesco
Srinivasan, Sudharsan
Jairath, Neil
Correa, Luis
Umemura, Yoshie
Walker, Angela
Kachman, Maureen
Qi, Nathan
Sarkaria, Jann
Xiong, Jianping
Morgan, Meredith
Rehemtulla, Alnawaz
Castro, Maria
Lowenstein, Pedro
Chandrasekaran, Sriram
Lawrence, Theodore
Lyssiotis, Costas
Wahl, Daniel
author_sort Zhou, Weihua
collection PubMed
description Intratumoral genomic heterogeneity in glioblastoma (GBM) is a barrier to overcoming radiation (RT) resistance. To discover genotype-independent mediators of RT resistance, we correlated RT resistance with the concentration of approximately 700 metabolites across 23 GBM cell lines. Purine metabolites, especially those containing the base guanine, were most correlated with RT resistance. Similarly, increased abundance of tumor purines was associated with decreased survival in GBM patients treated with RT. This relationship is causal. Purine supplementation protected RT-sensitive GBMs from RT and promoted the repair of RT-induced double strand DNA breaks (DSBs). In vitro and in vivo stable isotope tracing confirmed that GBM cell lines and orthotopic patient-derived xenografts primarily generated purines through the de novo synthetic pathway. RT treatment further increased de novo purine synthesis in GBM through signaling via the DNA damage response. Inhibition of de novo GTP synthesis with mycophenolic acid (MPA) sensitized multiple GBM cell lines and neurospheres to RT by slowing the repair of RT-induced DSBs. MPA-induced radiosensitization was GTP-dependent as it was rescued by nucleoside supplementation. Modulating pyrimidine metabolism affected neither RT resistance nor DSB repair, suggesting these GTP-specific effects are due to active signaling rather than its ability to act as a physical substrate for DNA repair and candidate signaling molecules have been identified. These results were recapitulated in vivo with mycophenolate mofetil (MMF), the orally bioavailable FDA-approved prodrug of MPA. MMF potentiated RT efficacy, reduced tumor guanylates and slowed the repair of RT-induced DSBs across multiple models. Because de novo purine synthesis is activated by many of the oncogenic alterations that drive GBM, its inhibition is a promising genotype-independent strategy to overcome GBM RT resistance. We have now begun a clinical trial to determine whether combining MMF and RT is safe and potentially efficacious in patients with GBM.
format Online
Article
Text
id pubmed-7992262
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-79922622021-03-31 DDRE-24. TARGETING PURINE METABOLISM TO OVERCOME GLIOBLASTOMA THERAPY RESISTANCE Zhou, Weihua Yao, Yangyang Scott, Andrew Wilder-Romans, Kari Dresser, Joseph Werner, Christian Sun, Hanshi Pratt, Drew Sajjakulnukit, Peter Zaho, Shuang Davis, Mary Nelson, Barbara Halbrook, Christopher Zhang, Li Gatto, Francesco Srinivasan, Sudharsan Jairath, Neil Correa, Luis Umemura, Yoshie Walker, Angela Kachman, Maureen Qi, Nathan Sarkaria, Jann Xiong, Jianping Morgan, Meredith Rehemtulla, Alnawaz Castro, Maria Lowenstein, Pedro Chandrasekaran, Sriram Lawrence, Theodore Lyssiotis, Costas Wahl, Daniel Neurooncol Adv Supplement Abstracts Intratumoral genomic heterogeneity in glioblastoma (GBM) is a barrier to overcoming radiation (RT) resistance. To discover genotype-independent mediators of RT resistance, we correlated RT resistance with the concentration of approximately 700 metabolites across 23 GBM cell lines. Purine metabolites, especially those containing the base guanine, were most correlated with RT resistance. Similarly, increased abundance of tumor purines was associated with decreased survival in GBM patients treated with RT. This relationship is causal. Purine supplementation protected RT-sensitive GBMs from RT and promoted the repair of RT-induced double strand DNA breaks (DSBs). In vitro and in vivo stable isotope tracing confirmed that GBM cell lines and orthotopic patient-derived xenografts primarily generated purines through the de novo synthetic pathway. RT treatment further increased de novo purine synthesis in GBM through signaling via the DNA damage response. Inhibition of de novo GTP synthesis with mycophenolic acid (MPA) sensitized multiple GBM cell lines and neurospheres to RT by slowing the repair of RT-induced DSBs. MPA-induced radiosensitization was GTP-dependent as it was rescued by nucleoside supplementation. Modulating pyrimidine metabolism affected neither RT resistance nor DSB repair, suggesting these GTP-specific effects are due to active signaling rather than its ability to act as a physical substrate for DNA repair and candidate signaling molecules have been identified. These results were recapitulated in vivo with mycophenolate mofetil (MMF), the orally bioavailable FDA-approved prodrug of MPA. MMF potentiated RT efficacy, reduced tumor guanylates and slowed the repair of RT-induced DSBs across multiple models. Because de novo purine synthesis is activated by many of the oncogenic alterations that drive GBM, its inhibition is a promising genotype-independent strategy to overcome GBM RT resistance. We have now begun a clinical trial to determine whether combining MMF and RT is safe and potentially efficacious in patients with GBM. Oxford University Press 2021-03-25 /pmc/articles/PMC7992262/ http://dx.doi.org/10.1093/noajnl/vdab024.046 Text en © The Author(s) 2021. Published by Oxford University Press, the Society for Neuro-Oncology and the European Association of Neuro-Oncology. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Supplement Abstracts
Zhou, Weihua
Yao, Yangyang
Scott, Andrew
Wilder-Romans, Kari
Dresser, Joseph
Werner, Christian
Sun, Hanshi
Pratt, Drew
Sajjakulnukit, Peter
Zaho, Shuang
Davis, Mary
Nelson, Barbara
Halbrook, Christopher
Zhang, Li
Gatto, Francesco
Srinivasan, Sudharsan
Jairath, Neil
Correa, Luis
Umemura, Yoshie
Walker, Angela
Kachman, Maureen
Qi, Nathan
Sarkaria, Jann
Xiong, Jianping
Morgan, Meredith
Rehemtulla, Alnawaz
Castro, Maria
Lowenstein, Pedro
Chandrasekaran, Sriram
Lawrence, Theodore
Lyssiotis, Costas
Wahl, Daniel
DDRE-24. TARGETING PURINE METABOLISM TO OVERCOME GLIOBLASTOMA THERAPY RESISTANCE
title DDRE-24. TARGETING PURINE METABOLISM TO OVERCOME GLIOBLASTOMA THERAPY RESISTANCE
title_full DDRE-24. TARGETING PURINE METABOLISM TO OVERCOME GLIOBLASTOMA THERAPY RESISTANCE
title_fullStr DDRE-24. TARGETING PURINE METABOLISM TO OVERCOME GLIOBLASTOMA THERAPY RESISTANCE
title_full_unstemmed DDRE-24. TARGETING PURINE METABOLISM TO OVERCOME GLIOBLASTOMA THERAPY RESISTANCE
title_short DDRE-24. TARGETING PURINE METABOLISM TO OVERCOME GLIOBLASTOMA THERAPY RESISTANCE
title_sort ddre-24. targeting purine metabolism to overcome glioblastoma therapy resistance
topic Supplement Abstracts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7992262/
http://dx.doi.org/10.1093/noajnl/vdab024.046
work_keys_str_mv AT zhouweihua ddre24targetingpurinemetabolismtoovercomeglioblastomatherapyresistance
AT yaoyangyang ddre24targetingpurinemetabolismtoovercomeglioblastomatherapyresistance
AT scottandrew ddre24targetingpurinemetabolismtoovercomeglioblastomatherapyresistance
AT wilderromanskari ddre24targetingpurinemetabolismtoovercomeglioblastomatherapyresistance
AT dresserjoseph ddre24targetingpurinemetabolismtoovercomeglioblastomatherapyresistance
AT wernerchristian ddre24targetingpurinemetabolismtoovercomeglioblastomatherapyresistance
AT sunhanshi ddre24targetingpurinemetabolismtoovercomeglioblastomatherapyresistance
AT prattdrew ddre24targetingpurinemetabolismtoovercomeglioblastomatherapyresistance
AT sajjakulnukitpeter ddre24targetingpurinemetabolismtoovercomeglioblastomatherapyresistance
AT zahoshuang ddre24targetingpurinemetabolismtoovercomeglioblastomatherapyresistance
AT davismary ddre24targetingpurinemetabolismtoovercomeglioblastomatherapyresistance
AT nelsonbarbara ddre24targetingpurinemetabolismtoovercomeglioblastomatherapyresistance
AT halbrookchristopher ddre24targetingpurinemetabolismtoovercomeglioblastomatherapyresistance
AT zhangli ddre24targetingpurinemetabolismtoovercomeglioblastomatherapyresistance
AT gattofrancesco ddre24targetingpurinemetabolismtoovercomeglioblastomatherapyresistance
AT srinivasansudharsan ddre24targetingpurinemetabolismtoovercomeglioblastomatherapyresistance
AT jairathneil ddre24targetingpurinemetabolismtoovercomeglioblastomatherapyresistance
AT correaluis ddre24targetingpurinemetabolismtoovercomeglioblastomatherapyresistance
AT umemurayoshie ddre24targetingpurinemetabolismtoovercomeglioblastomatherapyresistance
AT walkerangela ddre24targetingpurinemetabolismtoovercomeglioblastomatherapyresistance
AT kachmanmaureen ddre24targetingpurinemetabolismtoovercomeglioblastomatherapyresistance
AT qinathan ddre24targetingpurinemetabolismtoovercomeglioblastomatherapyresistance
AT sarkariajann ddre24targetingpurinemetabolismtoovercomeglioblastomatherapyresistance
AT xiongjianping ddre24targetingpurinemetabolismtoovercomeglioblastomatherapyresistance
AT morganmeredith ddre24targetingpurinemetabolismtoovercomeglioblastomatherapyresistance
AT rehemtullaalnawaz ddre24targetingpurinemetabolismtoovercomeglioblastomatherapyresistance
AT castromaria ddre24targetingpurinemetabolismtoovercomeglioblastomatherapyresistance
AT lowensteinpedro ddre24targetingpurinemetabolismtoovercomeglioblastomatherapyresistance
AT chandrasekaransriram ddre24targetingpurinemetabolismtoovercomeglioblastomatherapyresistance
AT lawrencetheodore ddre24targetingpurinemetabolismtoovercomeglioblastomatherapyresistance
AT lyssiotiscostas ddre24targetingpurinemetabolismtoovercomeglioblastomatherapyresistance
AT wahldaniel ddre24targetingpurinemetabolismtoovercomeglioblastomatherapyresistance