Evidence map›Paper›PMID 25970789›Full record

ArticleOncotarget2015

Proteomic profiling of high risk medulloblastoma reveals functional biology.

Jerome A Staal, Ling San Lau, Huizhen Zhang, Wendy J Ingram, Andrew R Hallahan, Paul A Northcott, Stefan M Pfister, Robert J Wechsler-Reya, Jessica M Rusert, Michael D Taylor and 4 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.4field-weighted citation impact, top 20% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

14 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
  2. Group-specific cellular metabolism in Medulloblastoma.Journal of translational medicine · 2023
    Article
  3. Review
  4. Article
  5. A systematic view of pediatric medulloblastoma proteomics-current state of the field and future directions.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2021
    Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Review
  13. Review
  14. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors at 7 institutions in 4 countries.

Jerome A StaalCenter for Cancer and Immunology Research, Children's National Medical Center, Washington DC, USA.
Ling San LauCenter for Cancer and Immunology Research, Children's National Medical Center, Washington DC, USA.
Huizhen ZhangCenter for Cancer and Immunology Research, Children's National Medical Center, Washington DC, USA.
Wendy J IngramUQ Child Health Research Centre, The University of Queensland and Queensland Children's Medical Research Institute, Children's Health, Queensland, Australia.
Andrew R HallahanUQ Child Health Research Centre, The University of Queensland and Queensland Children's Medical Research Institute, Children's Health, Queensland, Australia.
Paul A NorthcottDivision of Pediatric Neurooncology, German Cancer Research Center, Heidleberg, Germany.
Stefan M PfisterDivision of Pediatric Neurooncology, German Cancer Research Center, Heidleberg, Germany.
Robert J Wechsler-ReyaSanford-Burnham Medical Research Institute, La Jolla, California, USA.
Jessica M RusertSanford-Burnham Medical Research Institute, La Jolla, California, USA.
Michael D TaylorDepartment of Neurosurgery, Hospital for Sick Children, Toronto, Canada.
Yoon-Jae ChoDepartment of Neurology and Neurological Sciences, Stanford University School of Medicine, Stanford, California, USA.
Roger J PackerCenter for Neuroscience and Behavioral Medicine, Children's National Medical Center, Washington DC, USA.
Kristy J BrownCenter for Genetic Medicine, Children's National Medical Center, Washington DC, USA.
Brian R RoodCenter for Cancer and Immunology Research, Children's National Medical Center, Washington DC, USA.
Children's National · USGerman Cancer Research Center · DESanford Burnham Prebys Medical Discovery Institute · USChildren's Medical Research Institute · AUHospital for Sick Children · CAStanford University · USUniversity of Queensland · AU

Funding

NEUROIMAGING COREP30HD040677 · NICHD · CHILDREN'S RESEARCH INSTITUTE · PI VITTORIO GALLO, VITTORIO GALLO VITTORIO GALLO · 2001 to 2015
$15.9M
Clinical and Translational Science Institute at Children's NationalUL1TR000075 · NCATS · CHILDREN'S RESEARCH INSTITUTE · PI GUAY-WOODFORD, LISA MARIE · 2012 to 2015
$13.7M
CTSA INFRASTRUCTURE FOR PEDIATRIC RESEARCHUL1RR031988 · NCRR · CHILDREN'S RESEARCH INSTITUTE · PI GUAY-WOODFORD, LISA MARIE · 2010 to 2011
$8.2M
NCATS NIH HHS UL1 TR000075NCATS NIH HHS UL1TR000075NCRR NIH HHS UL1 RR031988NCRR NIH HHS UL1RR031988NICHD NIH HHS 5P30HD040677NICHD NIH HHS P30 HD040677
6 · The paper itself

Abstract

Genomic characterization of medulloblastoma has improved molecular risk classification but struggles to define functional biological processes, particularly for the most aggressive subgroups. We present here a novel proteomic approach to this problem using a reference library of stable isotope labeled medulloblastoma-specific proteins as a spike-in standard for accurate quantification of the tumor proteome. Utilizing high-resolution mass spectrometry, we quantified the tumor proteome of group 3 medulloblastoma cells and demonstrate that high-risk MYC amplified tumors can be segregated based on protein expression patterns. We cross-validated the differentially expressed protein candidates using an independent transcriptomic data set and further confirmed them in a separate cohort of medulloblastoma tissue samples to identify the most robust proteogenomic differences. Interestingly, highly expressed proteins associated with MYC-amplified tumors were significantly related to glycolytic metabolic pathways via alternative splicing of pyruvate kinase (PKM) by heterogeneous ribonucleoproteins (HNRNPs). Furthermore, when maintained under hypoxic conditions, these MYC-amplified tumors demonstrated increased viability compared to non-amplified tumors within the same subgroup. Taken together, these findings highlight the power of proteomics as an integrative platform to help prioritize genetic and molecular drivers of cancer biology and behavior.

Indexed as

Biomarkers, TumorCell Line, TumorCerebellar NeoplasmsHumansMass SpectrometryMedulloblastomaProteomicsRisk FactorsBiomarkers, TumorcancercMYCglycolysismedulloblastomaproteomics

Identifiers

PMID25970789
PMCPMC4546489
OpenAlexW2161889038

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.