Evidence map›Paper›PMID 19594892›Full record

ArticleJournal of translational medicine2009

A novel role of HLA class I in the pathology of medulloblastoma.

Courtney Smith, Mariarita Santi, Bhargavi Rajan, Elisabeth J Rushing, Mi Rim Choi, Brian R Rood, Robert Cornelison, Tobey J MacDonald, Stanislav Vukmanovic

Open access · goldAbstract read
In one paragraph

Article in Journal of translational medicine, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
0.5field-weighted citation impact, top 35% 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

18 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
  2. Medulloblastoma: biology and immunotherapy.Frontiers in immunology · 2025
    Review
  3. Article
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  9. Open MHC Class I Conformers: A Look through the Looking Glass.International journal of molecular sciences · 2021
    Review
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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

9 authors at 4 institutions in 1 country.

Courtney SmithCenter for Cancer and Immunology Research, Children's Research Institute, Children's National Medical Center, Washington, DC, USA. smithco@mlhs.org
Mariarita Santi
Bhargavi Rajan
Elisabeth J Rushing
Mi Rim Choi
Brian R Rood
Robert Cornelison
Tobey J MacDonald
Stanislav Vukmanovic
Children's National · USGeorge Washington University · USArmed Forces Institute of Pathology · USCancer Genetics (United States) · US

Funding

The Role of PDGFR in Medulloblastoma ProgressionR01CA111835 · NCI · EMORY UNIVERSITY · PI MACDONALD, TOBEY J. · 2006 to 2010
$1.3M
NCI NIH HHS R01 CA111835
6 · The paper itself

Abstract

backgroundMHC class I expression by cancer cells enables specific antigen recognition by the immune system and protection of the host. However, in some cancer types MHC class I expression is associated with an unfavorable outcome. We explored the basis of MHC class I association with unfavorable prognostic marker expression in the case of medulloblastoma.

methodsWe investigated expression of four essential components of MHC class I (heavy chain, beta2m, TAP1 and TAP2) in 10 medulloblastoma mRNA samples, a tissue microarray containing 139 medulloblastoma tissues and 3 medulloblastoma cell lines. Further, in medulloblastoma cell lines we evaluated the effects of HLA class I engagement on activation of ERK1/2 and migration in vitro.

resultsThe majority of specimens displayed undetectable or low levels of the heavy chains. Medulloblastomas expressing high levels of HLA class I displayed significantly higher levels of anaplasia and c-myc expression, markers of poor prognosis. Binding of beta2m or a specific antibody to open forms of HLA class I promoted phosphorylation of ERK1/2 in medulloblastoma cell line with high levels, but not in the cell line with low levels of HLA heavy chain. This treatment also promoted ERK1/2 activation dependent migration of medulloblastoma cells.

conclusionMHC class I expression in medulloblastoma is associated with anaplasia and c-myc expression, markers of poor prognosis. Peptide- and/or beta2m-free forms of MHC class I may contribute to a more malignant phenotype of medulloblastoma by modulating activation of signaling molecules such as ERK1/2 that stimulates cell mobility.

Indexed as

Biomarkers, TumorCerebellar NeoplasmsHistocompatibility Antigens Class IMedulloblastomaAnaplasiaCell Line, TumorEnzyme ActivationExtracellular Signal-Regulated MAP KinasesGene Expression Regulation, NeoplasticHumansImmunohistochemistryLeukocyte Common AntigensPrognosisProto-Oncogene Proteins c-mycBiomarkers, TumorExtracellular Signal-Regulated MAP KinasesHistocompatibility Antigens Class ILeukocyte Common AntigensProto-Oncogene Proteins c-myc

Identifiers

PMID19594892
PMCPMC2714836
OpenAlexW2166791024

What OpenQuestion holds

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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.