Cargando…

Combined MEK and JAK/STAT3 pathway inhibition effectively decreases SHH medulloblastoma tumor progression

Medulloblastoma (MB) is the most common primary malignant pediatric brain cancer. We recently identified novel roles for the MEK/MAPK pathway in regulating human Sonic Hedgehog (SHH) MB tumorigenesis. The MEK inhibitor, selumetinib, decreased SHH MB growth while extending survival in mouse models. H...

Descripción completa

Detalles Bibliográficos
Autores principales: Zagozewski, Jamie, Borlase, Stephanie, Guppy, Brent J., Coudière-Morrison, Ludivine, Shahriary, Ghazaleh M., Gordon, Victor, Liang, Lisa, Cheng, Stephen, Porter, Christopher J., Kelley, Rhonda, Hawkins, Cynthia, Chan, Jennifer A., Liang, Yan, Gong, Jingjing, Nör, Carolina, Saulnier, Olivier, Wechsler-Reya, Robert J., Ramaswamy, Vijay, Werbowetski-Ogilvie, Tamra E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9283517/
https://www.ncbi.nlm.nih.gov/pubmed/35835937
http://dx.doi.org/10.1038/s42003-022-03654-9
_version_ 1784747329803255808
author Zagozewski, Jamie
Borlase, Stephanie
Guppy, Brent J.
Coudière-Morrison, Ludivine
Shahriary, Ghazaleh M.
Gordon, Victor
Liang, Lisa
Cheng, Stephen
Porter, Christopher J.
Kelley, Rhonda
Hawkins, Cynthia
Chan, Jennifer A.
Liang, Yan
Gong, Jingjing
Nör, Carolina
Saulnier, Olivier
Wechsler-Reya, Robert J.
Ramaswamy, Vijay
Werbowetski-Ogilvie, Tamra E.
author_facet Zagozewski, Jamie
Borlase, Stephanie
Guppy, Brent J.
Coudière-Morrison, Ludivine
Shahriary, Ghazaleh M.
Gordon, Victor
Liang, Lisa
Cheng, Stephen
Porter, Christopher J.
Kelley, Rhonda
Hawkins, Cynthia
Chan, Jennifer A.
Liang, Yan
Gong, Jingjing
Nör, Carolina
Saulnier, Olivier
Wechsler-Reya, Robert J.
Ramaswamy, Vijay
Werbowetski-Ogilvie, Tamra E.
author_sort Zagozewski, Jamie
collection PubMed
description Medulloblastoma (MB) is the most common primary malignant pediatric brain cancer. We recently identified novel roles for the MEK/MAPK pathway in regulating human Sonic Hedgehog (SHH) MB tumorigenesis. The MEK inhibitor, selumetinib, decreased SHH MB growth while extending survival in mouse models. However, the treated mice ultimately succumbed to disease progression. Here, we perform RNA sequencing on selumetinib-treated orthotopic xenografts to identify molecular pathways that compensate for MEK inhibition specifically in vivo. Notably, the JAK/STAT3 pathway exhibits increased activation in selumetinib-treated tumors. The combination of selumetinib and the JAK/STAT3 pathway inhibitor, pacritinib, further reduces growth in two xenograft models and also enhances survival. Multiplex spatial profiling of proteins in drug-treated xenografts reveals shifted molecular dependencies and compensatory changes following combination drug treatment. Our study warrants further investigation into MEK and JAK/STAT3 inhibition as a novel combinatory therapeutic strategy for SHH MB.
format Online
Article
Text
id pubmed-9283517
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-92835172022-07-16 Combined MEK and JAK/STAT3 pathway inhibition effectively decreases SHH medulloblastoma tumor progression Zagozewski, Jamie Borlase, Stephanie Guppy, Brent J. Coudière-Morrison, Ludivine Shahriary, Ghazaleh M. Gordon, Victor Liang, Lisa Cheng, Stephen Porter, Christopher J. Kelley, Rhonda Hawkins, Cynthia Chan, Jennifer A. Liang, Yan Gong, Jingjing Nör, Carolina Saulnier, Olivier Wechsler-Reya, Robert J. Ramaswamy, Vijay Werbowetski-Ogilvie, Tamra E. Commun Biol Article Medulloblastoma (MB) is the most common primary malignant pediatric brain cancer. We recently identified novel roles for the MEK/MAPK pathway in regulating human Sonic Hedgehog (SHH) MB tumorigenesis. The MEK inhibitor, selumetinib, decreased SHH MB growth while extending survival in mouse models. However, the treated mice ultimately succumbed to disease progression. Here, we perform RNA sequencing on selumetinib-treated orthotopic xenografts to identify molecular pathways that compensate for MEK inhibition specifically in vivo. Notably, the JAK/STAT3 pathway exhibits increased activation in selumetinib-treated tumors. The combination of selumetinib and the JAK/STAT3 pathway inhibitor, pacritinib, further reduces growth in two xenograft models and also enhances survival. Multiplex spatial profiling of proteins in drug-treated xenografts reveals shifted molecular dependencies and compensatory changes following combination drug treatment. Our study warrants further investigation into MEK and JAK/STAT3 inhibition as a novel combinatory therapeutic strategy for SHH MB. Nature Publishing Group UK 2022-07-14 /pmc/articles/PMC9283517/ /pubmed/35835937 http://dx.doi.org/10.1038/s42003-022-03654-9 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Zagozewski, Jamie
Borlase, Stephanie
Guppy, Brent J.
Coudière-Morrison, Ludivine
Shahriary, Ghazaleh M.
Gordon, Victor
Liang, Lisa
Cheng, Stephen
Porter, Christopher J.
Kelley, Rhonda
Hawkins, Cynthia
Chan, Jennifer A.
Liang, Yan
Gong, Jingjing
Nör, Carolina
Saulnier, Olivier
Wechsler-Reya, Robert J.
Ramaswamy, Vijay
Werbowetski-Ogilvie, Tamra E.
Combined MEK and JAK/STAT3 pathway inhibition effectively decreases SHH medulloblastoma tumor progression
title Combined MEK and JAK/STAT3 pathway inhibition effectively decreases SHH medulloblastoma tumor progression
title_full Combined MEK and JAK/STAT3 pathway inhibition effectively decreases SHH medulloblastoma tumor progression
title_fullStr Combined MEK and JAK/STAT3 pathway inhibition effectively decreases SHH medulloblastoma tumor progression
title_full_unstemmed Combined MEK and JAK/STAT3 pathway inhibition effectively decreases SHH medulloblastoma tumor progression
title_short Combined MEK and JAK/STAT3 pathway inhibition effectively decreases SHH medulloblastoma tumor progression
title_sort combined mek and jak/stat3 pathway inhibition effectively decreases shh medulloblastoma tumor progression
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9283517/
https://www.ncbi.nlm.nih.gov/pubmed/35835937
http://dx.doi.org/10.1038/s42003-022-03654-9
work_keys_str_mv AT zagozewskijamie combinedmekandjakstat3pathwayinhibitioneffectivelydecreasesshhmedulloblastomatumorprogression
AT borlasestephanie combinedmekandjakstat3pathwayinhibitioneffectivelydecreasesshhmedulloblastomatumorprogression
AT guppybrentj combinedmekandjakstat3pathwayinhibitioneffectivelydecreasesshhmedulloblastomatumorprogression
AT coudieremorrisonludivine combinedmekandjakstat3pathwayinhibitioneffectivelydecreasesshhmedulloblastomatumorprogression
AT shahriaryghazalehm combinedmekandjakstat3pathwayinhibitioneffectivelydecreasesshhmedulloblastomatumorprogression
AT gordonvictor combinedmekandjakstat3pathwayinhibitioneffectivelydecreasesshhmedulloblastomatumorprogression
AT lianglisa combinedmekandjakstat3pathwayinhibitioneffectivelydecreasesshhmedulloblastomatumorprogression
AT chengstephen combinedmekandjakstat3pathwayinhibitioneffectivelydecreasesshhmedulloblastomatumorprogression
AT porterchristopherj combinedmekandjakstat3pathwayinhibitioneffectivelydecreasesshhmedulloblastomatumorprogression
AT kelleyrhonda combinedmekandjakstat3pathwayinhibitioneffectivelydecreasesshhmedulloblastomatumorprogression
AT hawkinscynthia combinedmekandjakstat3pathwayinhibitioneffectivelydecreasesshhmedulloblastomatumorprogression
AT chanjennifera combinedmekandjakstat3pathwayinhibitioneffectivelydecreasesshhmedulloblastomatumorprogression
AT liangyan combinedmekandjakstat3pathwayinhibitioneffectivelydecreasesshhmedulloblastomatumorprogression
AT gongjingjing combinedmekandjakstat3pathwayinhibitioneffectivelydecreasesshhmedulloblastomatumorprogression
AT norcarolina combinedmekandjakstat3pathwayinhibitioneffectivelydecreasesshhmedulloblastomatumorprogression
AT saulnierolivier combinedmekandjakstat3pathwayinhibitioneffectivelydecreasesshhmedulloblastomatumorprogression
AT wechslerreyarobertj combinedmekandjakstat3pathwayinhibitioneffectivelydecreasesshhmedulloblastomatumorprogression
AT ramaswamyvijay combinedmekandjakstat3pathwayinhibitioneffectivelydecreasesshhmedulloblastomatumorprogression
AT werbowetskiogilvietamrae combinedmekandjakstat3pathwayinhibitioneffectivelydecreasesshhmedulloblastomatumorprogression