Evidence map›Paper›PMID 27834580›Full record

ArticleCancer biology & therapy2016

NKG2D ligand expression in pediatric brain tumors.

Kristen Haberthur, Kathryn Brennan, Virginia Hoglund, Stephanie Balcaitis, Harrison Chinn, Amira Davis, Shannon Kreuser, Conrad Winter, Sarah E S Leary, Gail H Deutsch and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Cancer biology & therapy, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
0.6field-weighted citation impact, top 29% 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

23 citing papers in PubMed, 30 citations in OpenAlex.

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  7. Advances in NK cell therapy for brain tumors.NPJ precision oncology · 2023
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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

12 authors at 3 institutions in 1 country.

Kristen Haberthura Ben Towne Center for Childhood Cancer Research, Seattle Children's Research Institute , Seattle , WA , USA.
Kathryn Brennanb University of Michigan , Department of Immunology , Ann Arbor , MI , USA.
Virginia Hoglunda Ben Towne Center for Childhood Cancer Research, Seattle Children's Research Institute , Seattle , WA , USA.
Stephanie Balcaitisa Ben Towne Center for Childhood Cancer Research, Seattle Children's Research Institute , Seattle , WA , USA.
Harrison Chinna Ben Towne Center for Childhood Cancer Research, Seattle Children's Research Institute , Seattle , WA , USA.
Amira Davisa Ben Towne Center for Childhood Cancer Research, Seattle Children's Research Institute , Seattle , WA , USA.
Shannon Kreusera Ben Towne Center for Childhood Cancer Research, Seattle Children's Research Institute , Seattle , WA , USA.
Conrad Winterc Department of Pathology Seattle Children's Hospital , Seattle , WA , USA.
Sarah E S Learyd Seattle Children's Hospital and Associate Professor , Center for Clinical and Translational Research, Seattle Children's Research Institute , WA , USA.
Gail H Deutsche Fetal Autopsy Services, Department of Pathology , Seattle Children's Hospital , WA , USA.
Richard G Ellenbogenf University of Washington School of Medicine, Theodore S. Roberts Endowed Chair in Pediatric Neurological Surgery, Seattle Children's Hospital , WA , USA.
Courtney A Cranea Ben Towne Center for Childhood Cancer Research, Seattle Children's Research Institute , Seattle , WA , USA.
Seattle Children's Hospital · USUniversity of Michigan–Ann Arbor · USUniversity of Washington · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Adult brain tumors establish an immunosuppressive tumor microenvironment as a modality of immune escape, with several immunotherapies designed to overcome this barrier. However, the relationship between tumor cells and immune cells in pediatric brain tumor patients is not as well-defined. In this study, we sought to determine whether the model of immune escape observed in adult brain tumors is reflected in patients with pediatric brain tumors by evaluating NKG2D ligand expression on tissue microarrays created from patients with a variety of childhood brain tumor diagnoses, and infiltration of Natural Killer and myeloid cells. We noted a disparity between mRNA and protein expression for the 8 known NKG2D ligands. Surprisingly, high-grade gliomas did not have increased NKG2D ligand expression compared to normal adjacent brain tissue, nor did they have significant myeloid or NK cell infiltration. These data suggest that pediatric brain tumors have reduced NK cell-mediated immune surveillance, and a less immunosuppressive tumor microenvironment as compared to their adult counterparts. These data indicate that therapies aimed to improve NK cell trafficking and functions in pediatric brain tumors may have a greater impact on anti-tumor immune responses and patient survival, with fewer obstacles to overcome.

Indexed as

Brain NeoplasmsChildCytotoxicity, ImmunologicHistocompatibility Antigens Class IHumansImmunohistochemistryKiller Cells, NaturalLigandsMyeloid CellsNK Cell Lectin-Like Receptor Subfamily KRNA, MessengerTissue Array AnalysisTumor EscapeTumor MicroenvironmentHistocompatibility Antigens Class IKLRK1 protein, humanLigandsNK Cell Lectin-Like Receptor Subfamily KRNA, MessengerImmune privilegeimmune surveillanceimmunosuppressiveNK cellsNKG2D ligands

Identifiers

PMID27834580
PMCPMC5199167
OpenAlexW2555694983

What OpenQuestion holds

Textmetadata
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.