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Combined MEK and JAK/STAT3 pathway inhibition effectively decreases SHH medulloblastoma tumor progression.
- Source :
-
Communications biology [Commun Biol] 2022 Jul 14; Vol. 5 (1), pp. 697. Date of Electronic Publication: 2022 Jul 14. - Publication Year :
- 2022
-
Abstract
- 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.<br /> (© 2022. The Author(s).)
- Subjects :
- Animals
Child
Hedgehog Proteins genetics
Hedgehog Proteins metabolism
Humans
Mice
Mitogen-Activated Protein Kinase Kinases metabolism
Protein Kinase Inhibitors pharmacology
Protein Kinase Inhibitors therapeutic use
STAT3 Transcription Factor genetics
STAT3 Transcription Factor metabolism
Cerebellar Neoplasms drug therapy
Cerebellar Neoplasms genetics
Medulloblastoma drug therapy
Medulloblastoma genetics
Medulloblastoma metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 2399-3642
- Volume :
- 5
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Communications biology
- Publication Type :
- Academic Journal
- Accession number :
- 35835937
- Full Text :
- https://doi.org/10.1038/s42003-022-03654-9