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Characterization of an RNA binding protein interactome reveals a context-specific post-transcriptional landscape of MYC-amplified medulloblastoma
MM. Kameda-Smith, H. Zhu, EC. Luo, Y. Suk, A. Xella, B. Yee, C. Chokshi, S. Xing, F. Tan, RG. Fox, AA. Adile, D. Bakhshinyan, K. Brown, WD. Gwynne, M. Subapanditha, P. Miletic, D. Picard, I. Burns, J. Moffat, K. Paruch, A. Fleming, K. Hope, JP....
Jazyk angličtina Země Anglie, Velká Británie
Typ dokumentu časopisecké články, Research Support, N.I.H., Extramural, práce podpořená grantem
Grantová podpora
T32 HL086344
NHLBI NIH HHS - United States
T32 CA009523
NCI NIH HHS - United States
NLK
Directory of Open Access Journals
od 2015
Free Medical Journals
od 2010
PubMed Central
od 2012
Europe PubMed Central
od 2012
ProQuest Central
od 2019-01-01
Open Access Digital Library
od 2015-01-01
Open Access Digital Library
od 2015-01-01
Medline Complete (EBSCOhost)
od 2012-11-01
Health & Medicine (ProQuest)
od 2019-01-01
ROAD: Directory of Open Access Scholarly Resources
od 2010
Springer Nature OA/Free Journals
od 2010-12-01
Springer Nature - nature.com Journals - Fully Open Access
od 2010-12-01
- MeSH
- lidé MeSH
- meduloblastom * genetika MeSH
- myši MeSH
- nádory mozečku * genetika MeSH
- nádory mozku * MeSH
- proteiny nervové tkáně MeSH
- proteiny vázající RNA genetika MeSH
- proteomika MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- myši MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Research Support, N.I.H., Extramural MeSH
Pediatric medulloblastoma (MB) is the most common solid malignant brain neoplasm, with Group 3 (G3) MB representing the most aggressive subgroup. MYC amplification is an independent poor prognostic factor in G3 MB, however, therapeutic targeting of the MYC pathway remains limited and alternative therapies for G3 MB are urgently needed. Here we show that the RNA-binding protein, Musashi-1 (MSI1) is an essential mediator of G3 MB in both MYC-overexpressing mouse models and patient-derived xenografts. MSI1 inhibition abrogates tumor initiation and significantly prolongs survival in both models. We identify binding targets of MSI1 in normal neural and G3 MB stem cells and then cross referenced these data with unbiased large-scale screens at the transcriptomic, translatomic and proteomic levels to systematically dissect its functional role. Comparative integrative multi-omic analyses of these large datasets reveal cancer-selective MSI1-bound targets sharing multiple MYC associated pathways, providing a valuable resource for context-specific therapeutic targeting of G3 MB.
Centre for Discovery in Cancer Research McMaster University Hamilton ON Canada
Computational Biology Program Ontario Institute for Cancer Research Toronto Canada
Department of Biochemistry and Biomedical Sciences McMaster University Hamilton ON Canada
Department of Cellular and Molecular Medicine University of California at San Diego La Jolla CA USA
Department of Medical Biophysics University of Toronto Toronto Canada
Department of Molecular Genetics University of Toronto Toronto Canada
Donnelly Centre Department of Molecular Genetics University of Toronto Toronto Canada
McMaster University Department of Pediatrics Hamilton Canada
McMaster University Departments of Neuropathology Hamilton Canada
McMaster University Departments of Pediatrics Hematology and Oncology Division Hamilton Canada
Michael G DeGroote School of Medicine McMaster University Hamilton Canada
Sanford Consortium for Regenerative Medicine La Jolla CA USA
Stem Cell Program University of California San Diego La Jolla CA USA
Surgery Faculty of Health Sciences McMaster University Hamilton ON Canada
Citace poskytuje Crossref.org
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