Evidence map›Paper›PMID 30908480›Full record

ArticlePloS one2019

Suppression of Natural Killer cell NKG2D and CD226 anti-tumour cascades by platelet cloaked cancer cells: Implications for the metastatic cascade.

Christopher D Cluxton, Cathy Spillane, Sharon A O'Toole, Orla Sheils, Clair M Gardiner, John J O'Leary

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 64 papers.

0numbers the graph read from it
0cells of the map it votes in
64citing papers in PubMed
3.6field-weighted citation impact, top 6% 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

64 citing papers in PubMed, 84 citations in OpenAlex.

  1. Review
  2. Towards liquid biopsy-based analysis of antitumour immunity.Nature reviews. Clinical oncology · 2026
    Review
  3. Review
  4. Platelets as regulators of cancer immunity: mechanisms and therapeutic perspectives.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Review
  5. Review
  6. Review
  7. Review
  8. Hemostasis at the edge between physiology and cancer.Internal and emergency medicine · 2026
    Review
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  11. Review
  12. Article
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4 more citing papers are in PubMed but not listed here.

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

6 authors at 1 institution in 1 country.

Christopher D CluxtonDepartment of Histopathology, Trinity College Dublin, Dublin, Ireland.ORCID 0000-0002-5134-3279
Cathy SpillaneDepartment of Histopathology, Trinity College Dublin, Dublin, Ireland.ORCID 0000-0003-0358-5967
Sharon A O'TooleDepartment of Histopathology, Trinity College Dublin, Dublin, Ireland.
Orla SheilsDepartment of Histopathology, Trinity College Dublin, Dublin, Ireland.
Clair M GardinerTrinity Biomedical Sciences Institute, Trinity College Dublin, Dublin, Ireland.
John J O'LearyDepartment of Histopathology, Trinity College Dublin, Dublin, Ireland.
Trinity College Dublin · IE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tumour cell immune evasion is a principal hallmark of successful metastasis. Tumour cells in the vasculature adopt a platelet cloak that efficiently suppresses the innate immune system by directly inhibiting Natural Killer (NK) cells, which normally function to neutralise spreading cancers. Here we describe two novel mechanisms of tumour cell evasion of NK cell anti-tumour functions. The first, an 'immune decoy' mechanism in which platelets induce the release of soluble NKG2D ligands from the tumour cell to mask detection and actively suppress NK cell degranulation and inflammatory cytokine (IFNγ) production, concomitantly. This represents a double-hit to immune clearance of malignant cells during metastasis. The second mechanism, a platelet-derived TGFβ-mediated suppression of the CD226/CD96-CD112/CD155 axis, is a novel pathway with poorly understood anti-cancer functions. We have demonstrated that platelets robustly suppress surface expression of CD226 and CD96 on the NK cell surface and their associated ligands on the tumour cell to further enhance NK cell suppression. These highly evolved mechanisms promote successful tumour immune evasion during metastasis and provide a unique opportunity for studying the complexity of cellular interactions in the metastatic cascade and thus novel targets for cancer immunotherapy.

Indexed as

Tumor EscapeAntigens, CDAntigens, Differentiation, T-LymphocyteBlood PlateletsCell Line, TumorHistocompatibility Antigens Class IHumansImmunity, InnateInterferon-gammaKiller Cells, NaturalNectinsNeoplasm MetastasisNK Cell Lectin-Like Receptor Subfamily KReceptors, VirusSignal TransductionT Lineage-Specific Activation Antigen 1Antigens, CDAntigens, Differentiation, T-LymphocyteCD96 antigenHistocompatibility Antigens Class IInterferon-gammaKLRK1 protein, humanMHC class I-related chain AMICB antigenNectinsNK Cell Lectin-Like Receptor Subfamily Kpoliovirus receptorReceptors, VirusT Lineage-Specific Activation Antigen 1Transforming Growth Factor beta

Identifiers

PMID30908480
PMCPMC6433214
OpenAlexW2943263503

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.